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THE RELATIONSHIP OF SELF-CONCEPT AND


SOCIAL SUPPORT IN SCHOOL AGE
CHILDREN WITH LEUKEMIA

by
LISA DARLYNNE SOUTH

A DISSERTATION

Submitted in partial fulfillment of the requirements for


the degree of Doctor of Science in Nursing in the
School of Nursing in the Graduate S c h o o l ,
The University of Alabama at Birmingham

BIRMINGHAM, ALABAMA
1995

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DMI Number:

9527022

Copyright 1995 by
South, Lisa Darlynne
All rights reserved.

OMI Microform 9527022


Copyright 1995, by UMI Company. All rights reserved.
This microform edition is protected against unauthorized
copying under Title 17, United States Code.

UMI
300 North Zeeb Road
Ann Arbor, MI 48103

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Copyright by
Lisa Darlynne South
1995

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ABSTRACT OF DISSERTATION
GRADUATE SCHOOL, UNIVERSITY OF ALABAMA AT BIRMINGHAM

Degree

D.S.N_______________ Major Subject

Name of Candidate
Title

Maternal Child Nursing

Lisa Darlynne South_____________________________

The Relationship of Self-Concept and Social Support___________


in School Age Children With Leukemia__________________________
Since 1960 there have been many advances in the treat

ment of pediatric cancers. With the focus of care shifting


from prolonging remission to the reality of cure, the p s y
chosocial well being of the pediatric oncology client must
be addressed.

The purpose of this study was to describe

perceived social support and self-concept of school age


children with leukemia,

and to ascertain if there is a

relationship between social support and self-concept of


school age children with leukemia.

The Neuman Systems model

served as the organizing framework for the research.


A convenience sample of 17 school age children with
leukemia was recruited from pediatric oncology treatment
centers in the southeast.

The Piers Harris Children's Self-

Concept Scale and the Personal Resource Questionnaire,


2 were utilized for data collection.
of descriptive statistics,

Part

Data analysis consisted

stepwise multiple regression,

and

one-way analysis of variance.


Results of the research show that school age children
with leukemia with lower levels of perceived social support
iii

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are significantly more likely to have lower self-concept in


comparison to children with higher perceived social support.
Perceived social support of the sample was moderate to high.
Self-concept of the sample was average to high. There was a
strong positive relationship between social
self-concept of school

support and

age children with leukemia.

By c o n

trolling for race and sex, nearly one half of the variance
in self-concept was accounted for by social support.
Implications included teaching client and family s t r a t
egies for dealing with disease specific social situations.
Positive and effective coping strategies should be i de nti
fied and reinforced from the point of diagnosis and t rea t
ment initiation.

Crisis points,

and relapse of disease,

such as remission induction

can be anticipated,

and intervention

efforts can be intensified in preparation for these crisis


points.

Children at increased risk for psychosocial

should be identified,

problems

and more intense attention should be

focused on those children.


Further study of self-concept and social

support in

children should include children with solid tumors,


as hematogenous malignancies,
ic illnesses.

as well

and children with other chron

The Neuman Systems Model would be of benefit

as a guiding theoretical

framework.
)

Abstract Approved by:

Committee Chairman
Program Director _

Date

Dean of Graduate Si

iv

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DEDICATION
I wish to thank the children with cancer who
participated in this research.
Clay.

I am especially thankful to

I would not be where I am today without these

children.

I am grateful

for having known them all.

dedicate this work, and its continuation,

to them.

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ACKNOWLEDGMENTS
I am especially grateful

to committee members,

especially my chairperson, Dr. Kathy Jimmerson, who provided


me with support and encouragement at every step.

It is with

great appreciation that I acknowledge Dr. Penny Wright,


whose support,

expertise, and encouragement motivated me to

complete my work. Appreciation is also extended to Dr. Ann


Edgil, Dr. Rathi Iyer, Dr. Beth Stullenbarger,
Claypool

for their continued support,

and Dr. John

encouragement,

and

constant but gentle nudging to complete this work.


For their interest,

time, and cheerleading,

I thank the

faculty of 346 and the staff of 5SE. Their support and


encouragement are greatly appreciated.
Special thanks must go to Ann Douglas, who has shared
much of this experience with me and provided continuous
emotional support. Also,

for his computer expertise and for

always coming through in crisis,

I would like to thank Art

Drott.
I am grateful to God for His blessings of wisdom,
patience, and ability.

I am most grateful

to God for

allowing me to work with children with cancer.

vi

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TABLE OF CONTENTS
Page
ABSTRACT

....................................................

iii

DEDICATION ...................................................

ACKNOWLEDGEMENTS
LIST OF TABLES

...........................................

vi

.............................................

ix

........................................

Chapter
I

Introduction

Purpose ............................................
Research Questions ...............................
Assumptions .......................................
Delimitations .....................................
Theoretical Framework ............................
Definition of Terms ..............................
Significance ......................................
S u m m a r y ............................................
II

III

IV

Review of R e s e a r c h ..................................

3
3
4
4
4
14
15
17
18

Self-Concept and Chronic Illness


...............
Psychosocial Responses to Childhood Cancer
...
Social Support and Health
......................
Self Concept and Childhood Cancer
.............
Summary ...........................................

18
22
29
37
39

M e t h o d o l o g y ...........................................

41

D e s i g n .............................................
Instrumentation ..................................
S u b j e c t s ...........................................
S e t t i n g ............................................
Procedure for Data C o l l e c t i o n ..................
A n a l y s i s ...........................................
L i m i t a t i o n s .......................................
S u m m a r y ............................................

41
41
46
46
47
48
49
50

F i n d i n g s ..............................................
vii

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51

TABLE OF CONTENTS (Continued)


Chapter

Rqg
Description of Subjects .........................
Analysis of the D a t a .............................
Incidental Findings ..............................
S u m m a r y ............................................

51
52
56
59

Summary, Discussion, Conclusions, Implications


and Recommendations ..............................

61

S u m m a r y ............................................
D i s c u s s i o n .........................................
Limitations ......................................
C o n c l u s i o n s .......................................
Implications ......................................
Recommendations ...................................
References

....................................................

61
63
67
67
68
68
70

Appendices
A

Institutional R eview B o a r d Approval Forms

Program Director Approval

Guidelines for A d m i n ist ra tio n of Research Tools ...

85

Cover Letter ..........................................

89

Demographic Qu estionnaire/Consent

91

Form

........

....................

.................

viii

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79
83

LIST OF TABLES
Table
1

Page
Frequency Distribution of Subjects by Age,
Race, and Sex
....................................

52

Descriptive Statistics for Self-Concept Scores.

53

Frequencies for Social Support Scores

55

Stepwise Multip le Regression Summary for


Self-Concept Total
Scores.......................

55

Stepwise Mu ltple Regression Summary for


Behavior Subscale
..........................

56

Stepwise Multiple Regression Summary for


............
Happiness and Satisfaction Subscale

56

Descriptive Statistics for the Mean Self-Concept


Score by Levels of Perceived Social Support ...

57

Self-Concept and
Stage of Therapy

Social Support by
................................

57

Self-Concept

and

Social Support by Race

......

58

10

Self-Concept

and

Social Support by Age

.......

58

11

Self-Concept

and

Social Support by Sex

.......

59

........

ix

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Chapter I
Introduction
Since 1960 there have been many advances in the treat
ment of pediatric cancers. Childhood cancers once viewed as
fatal can now be cured. Approximately 6,000 new diagnoses of
childhood malignancies are made each year. Of this number,
at least one half of these children will be cured of their
disease (Hockenberry, Coody,

S Falletta,

1986). Due to

prolonged survival and increased cure rates,

the child with

cancer requires nursing interventions that, in the past,


were not necessary (Hockenberry, Coody,

& Bennett,

1990).

Long-term psychological sequelae of cancer diagnosis and


treatment,

such as negative effects on the developing self-

concept, have only recently become topics of research.


Advances in therapy have prolonged the life expectan
cies of children with cancer.

In the 1940s, children with

acute lymphocytic leukemia died within a few months of


diagnosis. More than 50% of the children now diagnosed with
this disease will survive 5 or more years disease free
(Howell,

1981). By the year 2000 more than 1 in every 1,000

young adults will have survived childhood cancer


Kazak,

& Meadows,

(Greenberg,

1989). As the medical outlook for ch i l d

hood cancer continues to improve and childhood cancer b e


comes a chronic rather than fatal acute condition, many

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2
psychosocial

responses are evolving (Van Dongen-Melman &

Sanders-Woudstra,

1986).

W i t h the focus of care shifting from prolonging remis


sion to the reality of cure, the psychosocial well being of
the pediatric oncology client must be addressed.

Normal

growth and development must be fostered despite the s t r e s s


ors of childhood cancer.

Frequent intensive drug therapy,

painful and invasive procedures,


hospitalizations,

social

influence personal

frequent clinic visits and

isolation,

and long-term adjustment

responses to cancer (Micheal

& Copeland,

1987). Quality of life for the child with cancer should be


evaluated by psychological
Body changes,
stomatitis,

cure as well

as biological

such as weight gain or loss,

amputation,

sterility,

and changes in intellectual

cure.

alopecia,

skeletal abnormalities,

functioning,

are common side

effects of cancer therapy. These changes are constant re


minders to children with cancer that they are different from
their peers.

It is assumed that the basic developmental

course proceeds despite the stressors of cancer;


course might be altered by the cancer experience.

yet, the
Research

is lacking regarding the emotional aspects of living with


childhood cancer

(Van Dongen-Melman & Sanders-Woudstra,

1986). There is little research dealing with self-concept of


children with cancer or with childhood cancer survivors.
Secondary to advances in the treatment of childhood
cancer,

children face psychological stressors previously

unidentified when children with cancer universally died

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shortly after diagnosis.


include germ phobias,
related to therapy,

Lon g-t erm psychological sequelae

s el f-e ste em problems,

and depression

delayed puberty

(Koocher,

1986).

School

phobia is 10 times greater in children with cancer than that


in the general

population

Hockenberry

(Klopovich,

1983).

(1986) defines crisis points in pediatric

cancer as apparently unsolvable problems caused by stressful


events,

which lead to loss of individual

equilibrium.

lution of stress is possible only when the individual

Reso
is

able to re-establish equilibrium. Hockenberry identified


crisis points in pediatric cancer as diagnosis,
discontinuation of therapy,
However,

relapse,

treatment,

and end stage disease.

the degree of influence exerted by the stressors of

diagnosis,

treatment,

and living with cancer,

fects of these stressors on social


self-concept,

and the e f

support and the child's

are worthy issues for further study.

Purpose
The purpose of this research was to describe perceived
social support and self-concept of school

age children with

leukemia, and to ascertain if there is a relationship b e


tween social

support and self-concept in school

age children

with leukemia.
Research Questions
The research questions generated for this study i n c l u d
ed:

(a) What is the self-concept of school age children with

leukemia?

(b) What is the perceived social support of school

age children with leukemia?

(c)

Is there a relationship

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4
between social support and self-concept in school age chi l
dren with leukemia?
Assumptions
Assumptions inherent in this study include:
stressors of cancer diagnosis and its therapy,
self-concept of school age children,

(a) The

impact the

(b) the stressors of

cancer diagnosis and treatment effect the perceived social


support of school age children,

(c) accurate self-report

measures of self-concept can be obtained from school age


children
social

(d) accurate self-report measures of perceived

support can be obtained from school age children,

and

(e) responses to the items contained in the research tools


are an accurate reflection of the individual's self-concept
and social support.
Delimitations
This research was limited to school age children a t
tending pediatric oncology clinics of two major treatment
centers in the southeastern states. Uncontrollable extrane
ous variables,

which m a y influence alterations in self-

concept and social support,

include absence or death of a

family member, media presentation content, previous coping


strategies,

and mental

Theoretical

Framework

The theoretical

ability and education.

framework for this research was the

Neuman Systems model

(Neuman,

1989). The concept of concern

is the self-concept.

It is hypothesized that social support

may help to explain some of the variance in self-concept.

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Neuman Systems M o d e l . The Neuman Systems model

focuses

on the person and the person's responses to stressors.


person is described as a multidimensional

composite of

biological,

spiritual,

psychological,

developmental variables.

sociocultural,

The

and

The interrelationships of these

variables and the lines of normal defense determine the


degree of resistance a person has to stressors

(Neuman,

1989).
Every person has a central core of basic survival
characteristics.
defense,

Lines of resistance,

the normal

line of

and flexible lines of defense form boundaries for

this core. Stressors vary in their potential to disrupt the


normal

line of defense.

In this holistic approach,

person is able to make specific,

the

unique choices in response

to the stressors of the environment

(Neuman,

1989).

The

person is in a constant state of dynamic equilibrium with


the environment. Neuman defines the environment as the
internal

and external forces surrounding the person.

Based

on N e u m a n s broad definition of the environment and the


focus on stress, Ross and Bourbannais

(1985) speculate that

the environment is composed of stress factors. According to


Neuman, stress is any stimulus producing tension.

Stress has

the potential to cause or intensify illness by disrupting


the person's equilibrium.
Health is a steady state of equilibrium determined by
the biological, psychological,
developmental variables.

sociocultural,

spiritual,

and

It is a process of becoming that

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develops over time. H ealth is a reflection of the person's


level of wellness

(Neuman,

1989). This definition allows for

individual differences so that health is not a perfect


state, but the best possible state for the individual
given time

(Whall,

at any

1983). W i thi n the Neuman model, nursing

focuses on the total person and is concerned with all the


variables that stress the person.

Nursing's objective is to

assist the person in maintaining maxi mum health by stre ngt h


ening adaptation,

decreasing encounters with stressors,

and

reducing the effects of stressors that cannot be avoided


(Neuman,

1989).

Utilizing Neuman's model,

the nurse must focus on the

total client system and the system's reactions to stressors.


The client system may consist of an individual
clude significant others.

or may i n

The goals of pediatric nursing are

directed at assisting the client system in attaining optimal


wellness in order to progress through the stages of d e vel op
ment appropriately.
General

reactions to the stressors of cancer depend on

the developmental
capacity,

stage of the child, previous adaptive

the degree of pain and perceived mutilation,

meaning of the illness to the child and family,


child relationship,
in equilibrium.

the

the parent-

and the child's reactions to the change

The nurse must be cognizant of what the

individual is capable of accomplishing developmentally,


physically,

psychologically,

socioculturally,

and spi ritual

ly.

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Children are in constant change and m o tio n resulting


from continuous interaction wit h the environment.

Stressors

associated wi th pe diatric cancer penetrate the normal and


flexible lines of defense,

through the lines of resistance,

to invade the core of the individual


ors may affect the biological,
spiritual,

and developmental

individual.

Stressors,

of both are most


individual,

and the family.

psychological,

Stres s

sociocultural,

variables that make up the

coping strategies,

and the appraisal

likely to be directly controlled by the

so they are the most amenable to change through

health promotion efforts

(Neuman,

S e l f - c o n c e p t . Shavelson,

1989).

Hubner,

and Stanton (1976)

broadly defined self-concept as perceptions of self inf lu


enced by environmental
ers.

reinforcements and significant oth

Self-concept is inferred from a person's physical

symbolic responses to situations.


influence actions.
perceptions.

In turn,

or

One's self-perceptions

actions influence o n e s s e l f

These authors identified seven aspects of self-

concept as hierarchial, multifaceted,


developmental,

valuative,

organized,

relatively stable,
and differentiable.

Neuman (1989) does not explicitly define self-concept.


However,

an inference can be made from Neuman's model

that

self-concept is influenced through experience with the


environment. The environmental

influence is implicit in many

of the definitions of self-concept to be discussed.


Self-concept is learned and is an extremely important
aspect of growth and development.

Cooley (1912)

stated that

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self-concept is consequentially influenced by what indi vi du


als believe others to think of them. Felker (1974) defined
self-concept as the unique perceptions,
an individual has about the self.

ideas,

Further,

the sum total view one holds of oneself


Self-concept is defined by Burns

and attitudes

self-concept is

(Felker,

1974).

(1979) as m u l t i d i m e n

sional, being composed of what one thinks one is, what one
thinks that others think of oneself, what one thinks one can
become,

and what one would like to become.

unique and personal

Self-concept is

to each i n d i v i d u a l . It is a dynamic

valuative process whereby personal development evolves


through transactions with both the internal and external
environment

(Burns,

1979).

Self-concept consists of two levels.

The basic level

of

self-concept is learned and is relatively stable as age


increases.

The functional

level is continuously evolving

with each new relationship and situation.


levels,

Based on these

it can be surmised that self-concept develops over

time through an individual's perceptions of exchanges with


the social

environment

(Foltz,

1987). This view of self-

concept is consistent with Neuman's systems model

(Neuman,

1989).
There are many theories that describe self-concept.
Common to all theories is the belief that self-concept is an
abstract quality with cognitive and affective components.
Self-concept is learned as the result of experience and,
some extent,

to

is a determinant of behavior.

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Self-concept is useful in coping with chronic illness


and achieving psychological,

as well as biological,

cure. As

defined by van Eys (1987), psychological cure is acceptance


of having had cancer in one's past without evidence of
influence on education,

growth, and development. As new

treatment methods are refined and the numbers of survivors


of childhood cancer increase,

the pediatric client must be

assisted in adjusting emotionally,

intellectually, psych oso

cial ly, and developmentally to life with a chronic illness


(Klopovich,

1983).

Psychosocial responses to childhood cancer and its


treatment are essentially unstudied areas. However,
edge of psychosocial

kn owl

responses to childhood cancer stressors

is necessary so that psychological


(Koocher, O'Malley, Gogan,

cure can be achieved

& Foster,

cal phenomenon of self-concept,

1980). The psychologi

in its multidimensions,

is

the focus of this study.


Social support.

The environment is composed of the

internal and external

forces surrounding a person. The

environment consists of all factors affecting or affected by


an individual

(Neuman,

1989).

Social support can be viewed

as an environmental variable potentiating or alleviating


stress for an individual.

Social support is differential,

comprehensive, multidimensional,
1985). Social

and parsimonious

support is viewed as informal,

noncontractual.

(V eiel,

reciprocal,

and

It also acts to buffer stress by preventing

or reducing stress effects

(Tilden 6. W e i n e r t , 1987).

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10

Social support may meet individual needs by fulfilling


the social

functions of social

integration,

attachment,

nurturance, guidance in difficult circumstances,


ance of self-worth (Alloway & Bebbington,

or reassur

1987). Cohen and

Syme (1985) define social support as the resources provided


by others. This help provided by others may be in the form
of feedback, validation,
extent,

or satisfaction of needs. To some

our emotional well being is dictated by the support

of significant others

(Galanter,

1988).

Kane (1988) views negative supports as stressors so


that social support is entirely positive,
nurturing.

encouraging,

and

Cobb (1976) defined social support as information

that leads one to believe that they are loved, cared for,
valued,

and a member of a network with mutual

Social support, as defined by Cobb,


support,

esteem support,

includes emotional

and network support.

ly omitted tangible or material

obligations.

Cobb explicit

support from his definition.

An inductive definition of social support is offered by


Gottlieb (1978), who includes tangible support in three of
four categories of social support.
emotionally sustaining behavior,
ence,

environmental

action,

These categories include

indirect personal

influ

and problem-solving behavior.

In

1981, Gottlieb described social support as supporting the


three constructs of social integration,
interactions,
Weinert

social network

and access to resources in peer relationships.

(1987) considered social support to be composed of

provisions for attachment;

social

integration;

opportunities

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11

for nurturing behavior;


accomplishment;

reassurance of individual worth and

and informational, material,

and emotional

aid.
According to Caplan (1974),
mastery of the environment.

social support facilitates

Social

support is a pattern of

ties serving to m aintain psychological and physiological


integrity.

Individuals who receive consistent feedback about

behavior and performance,

and information about resources,

are able to cope most effectively with environmental st r e s s


ors. This definition of social support is difficult to
operationalize but

lends support to the n otion that social

support prevents or reduces the negative effects of stress


on health.
Lin, Dean,

and Ensel

(1986) break down social

into the two concepts of social and support.

support

The social

component reflects the connection of the individual


social

environment at varying levels of intimacy.

to the

The s u p

port component reflects activities deemed to be in strumen


tal,

expressive,

and essential.

Social support is further

seen as attachments serving to promote emotional mastery,


offer guidance,

or provide identity and performance feedback

to the i n d i v i d u a l .
Social

support can be viewed as a coping strategy in

the face of stress. Mutually reciprocated social support is


not protective

(Tilden,

1985).

Several m odels have been

suggested that serve to explain the relationship among


stress,

social

support,

and coping

(Roberts,

1988).

Coping

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12

and social support may function as a barrier to stressors.


Social support and coping may alter health habits influ enc
ing symptoms.

Coping and social

support may also alter

adjustment to the stressors of illness. Roberts states that


self-concept is highly related to social support and may be
related to the measurement and presence of social
Malone

support.

(1988) suggests that social network is an u m

brella concept encompassing social support.

Social support

consists of the positive outcomes occurring within the


social network.

According to Malone,

social support and

social dissupport exist along a fluid and dynamic continuum.


Social support generates self-concept and assists the i n d i
vidual

in assuming proper societal

roles.

Social support may

play a part in protecting the self-concept,


stressful

life conditions

(Malone,

especially under

1988).

Stress occurs when situational demands surpass one's


ability to cope with given events.
characteristic of the social

Social

support is a

environment that acts to c u s h

ion the effects of stressors by lessening the severity of


the reaction to the stressor,
efforts,

and empowering the individual

stressor as less stressful


ment,

enhancing individual

including social

overall physical
O'Reilly-Knapp,

(Northouse,

support,

to perceive the
1988).

is a potential

and psychological well being


1994). The loss of social

The envir on
resource for
(Cobb,

1976;

support can be a

factor in both physical disease and psychological


(Bruhn & Phillips,

coping

stress

1984).

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13

The literature suggests that social support may play an


important function in coping with cancer diagnosis and
treatment.

Social support plays a critical

role in mediating

the effects of cancer on both family units and individuals.


The loss of social support has been associated with cardio
vascular disease,

accidental injury, suicide, mental ill

ness, school phobias,

cancer,

and gastrointestinal di so r

ders. This suggests that social support may be a source of


prevention.

Social support has been shown to modify the

effects of negative stress as well as to strengthen hope.


social support is positive,

If

it enhances health and well

being. The ability to reciprocate social support is affected


by numerous factors including age, sex,
self-concept

(Bruhn 8 Phillips,

learned coping,

and

1984).

Social support exists everywhere and in everyone by


some definition. As the individual's environment changes,
the individual grows and develops,
support,

or

the need for social

and use of social support changes.

Change in p h y s i

cal and psychosocial functioning of the individual

can

affect their perception of the need and availability of


social support.

If an individual does not perceive that

social support is available,


Phillips,

it cannot be utilized (Bruhn &

1984).

Social support may serve to explain m u c h of the u n e x


plained variance of self-concept in this study.
the multidimensional

Therefore,

concept of social support is included

in this study.

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14

Definition of Terms
For the purpose of this research the following d ef ini
tions are provided:
1. Self-concept--a multidimensional composite of unique
perceptions,

attitudes,

and ideas that an individual de vel

ops about the self. This composite develops over time


through transactions between the self and the environment.
Self-concept is the unique and personal sum total view one
holds of oneself.
the individual

Operationally,

self-concept is defined as

total score on the Piers-Harris Children's

Self-Concept Scale (Piers & Harris,

1969).

2. Social support--Information that one is cared for


and loved, esteemed and valued,
a network or community of mutual
Social

and a sense of belonging to


obligation (Cobb,

support is described as empathy,

nurturance, behavior,

1976).

encouragement,

and information that confirms reci

procity and recognition of competence.


support is defined as the individual

Operationally,

social

score obtained on the

Personal Resource Questionnaire Part 2 (Brandt & W e i n e r t ,


1985).
3. School

age children--Children 8 to 12 years of age

without obvious physical

or mental

limitations who are or

have been receiving anticancer therapy at one of two major


pediatric oncology treatment centers.
4. Leuk emi a--Oncological disorder affecting the bone
marrow and specifically confirmed by appropriate pathology
and laboratory evaluation.

Leukemia is the most common

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15

cancer diagnosis in children age 2 to 9 years. Types of


leukemia include acute lymphocytic leukemia,
phocytic leukemia,

and T-cell

acute nonlym-

leukemia.

Significance
The A m er ic an Nurses'

Association

(1980) defines nursing

as the "diagnosis and treatment of human responses to actual


or potential heal th problems"

(p.9). The primary focus of

nursing is the prevention of illness and the maintenance of


optimal health.

The American Nurses' Assoc iat ion also notes

the need for n u rsi ng research to identify determinants of


wellness and heal th functioning,
Social support relates health,

such as social support.

environment,

which guide the discipli ne of nursing


& Kuo, 1979).

(Lin,

and person,
Simeone,

Ensel,

The Associ ati on of Pediatric Oncology Nurses

has also selected late effects of childhood cancer and l on g


term sequelae as research priorities for the future
(Education Committee, A sso cia ti on of Pediatric Oncology
Nurses,

1985; Hinds et a l ., 1990; Hinds et a l ., 1994).

The results of this research are useful


education,

practice,

and research.

in nursing

Nurses need to know what

to include when educating the client and the family regard


ing care of the child w ith cancer.

Educators need to know

what to teach n ursing students to provide the best client


outcomes for children with cancer.
The basis for future interpersonal
during the school

relations is laid

age years. The extent to w hich pediatric

cancer and its treatment interferes with social peer

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16

relations may determine the overall compromise of psyc ho so


cial adaptation with associated long-term consequences
(LaGreca,

1990).

Social support may be a critical


and maintenance of health.

factor in prevention

Specific interventions need to be

recognized that may require high levels of individualization


for total cure of the child wi th cancer to occur.

If a

relationship between self-concept and social support can be


supported,

children at risk for less than optimal

can be identified,

outcomes

and a foundation can be developed upon

which to base nursing interventions.

Data obtained from

clients could assist nursing educators and practicing nurses


in better meeting the needs of the child with leukemia.
It is obvious that the diagnosis and treatment of
childhood cancer have the potential
psychological,
disruption.

sociocultural,

for physiological,

spiritual,

and developmental

Total cure of the child with cancer involves

treating the child as a cancer survivor from the point of


diagnosis.
Children with cancer have an increased risk for p s y c h o
social maladaptation,

underscoring the need to identify the

risks and protective factors that may help explain indiv idu
al differences.

The multitude of chronic stressors b o mb ard

ing the child with cancer interact to impede psychosocial


adjustment. The child with cancer must be physically and
emotionally capable of handling teasing,
tions,

comments,

ques

and innuendos from peers in addition to coping with

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17

their own concerns about feeling different and unattractive.


Studying the relationship of psychological adjustment,
including self-concept,

with perceived social support may

lead to better understanding of the resilience of the child


with cancer.

Studies of self-concept and social support may

provide empirical evidence for the development of cognitive


behavioral

interventions to prevent or decrease psychosocial

maladaptation (Varni, Katz, Colegrove,

& Dolgin,

1994).

It is essential that the pediatric oncology nurse have


a sound scientific basis for anticipatory guidance and
interventions into actual and potential

alterations of self-

concept and its relationship with social support.

The rela

tionship between self-concept and social support must be


confirmed and fully understood in the child with leukemia so
that survivors will truly be cured.
Summary
In this chapter,

the purpose of the research was s t a t

ed. Research questions were formulated,

and the theoretical

basis for the research was reviewed. Finally the signifi


cance of the study was addressed.

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Chapter II
Review of Research
The purpose of this research was to ascertain if there
is a relationship between self-concept and social support in
school

age children with leukemia. A review of research was

conducted to support the study.

Self-concept and self-esteem

are considered identical concepts in the majority of the


literature and so are used interchangeably in the review of
research.

Limited research has been reported describing the

psychological

effects of childhood cancer. Areas of review

included self-concept and chronic illness,


responses to childhood cancer,

psychosocial

social support and health,

and the relationship of self-concept and childhood cancer.


The terms self-concept and self-esteem are used i nterchange
ably throughout much of the literature and are considered
synonymous for the purpose of this review of research.
Self-Concept and Chronic Illness
Robinson,
cial

Greene,

and Walker

(1988) studied p s y c hos o

factors possibly associated with recurrent somatic

complaints in 115 adolescents seen for the first time.


Adolescents with functional

complaints had significantly

greater negative life events,

lower self-esteem,

and a lower

self-evaluation than those adolescents coming for routine


health care.

It was concluded that functional somatic


18

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19

complaints are associated with poor psychosocial


in reaction to stressful

adjustment

life events and m ay result in poor

self-esteem in adolescents.
Self-esteem expresses approval

or disapproval

of o n e

self and is used interchangeably with self-concept as p o i n t


ed out by Riffee (1980). Riffee studied se lf-esteem in
hospitalized school age children undergoing surgery,
age children in the hospital,
hospitalized.
12 years.

school

and school age children not

The sample consisted of 63 children,

age 9 to

Total self-esteem scores were lower for the c h i l

dren hospitalized for surgery than either of the other


groups. This finding is applicable to pediatric oncology
because many children with solid tumors must undergo repeat
ed surgery for tumor debulking and staging.
Beddell, Giordani, Amour,

Tavormina,

and Boll

(1977)

examined the relationship of self-concept and the stresses


of life in chronically ill children.
the chronically ill completed several

Children at a camp for


tools including the

Piers-Harris Children's Self-Concept Scale (Piers & Harris,


1969). Children with low life stress had a more positive
self-concept and scored higher in the subscales of behavior,
intellectual
attributes,

and school status,


popularity,

physical appearance and

and happiness and satisfaction.

Both

the low life stress and the high life stress groups scored
equally on the anxiety subscale.

The low life stress group

experienced fewer health problems than the high stress


children.

The authors concluded that social and

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20

environmental

influences were important in determining the

psychological well being of chronically ill children. Highly


stressed,

chronically ill children evaluate themselves

negatively. The presence of chronic illness in childhood is


not sufficient to produce psychopathology but does increase
the risk and increases vulnerability to the stressors of
life (Beddell et a l ., 1977).
The self-concept of children with cerebral palsy,

age 4

to 8 years, was found to be similar to the self-concept of a


control group in a study conducted by Teplin, Howard,

and

O'Connor (1981). While the children in both groups rated


themselves similarly,

teachers rated the handicapped c h i l

dren as having lower self-concept than the control

subjects.

Parent ratings of the behavior of their children revealed no


group differences in self-concept.

The researchers concluded

that children may begin to regard themselves as different as


early as the age of 4 years,
permanent or obvious until
Several

but these views do not become

the child is school age.

studies found no differences in self-concept

and psychosocial

functioning among children with a chronic

illness. Tavormina, Kastner,

Slater,

and Watt

(1976) c o n

ducted standardized psychological assessments of children


with diabetes,

asthma,

and cystic fibrosis.

The overall

pattern of scores obtained demonstrated normalcy rather than


deviancy. Wadden,

Foster,

and Brownell

(1984) found no

significant differences in Piers-Harris Children's SelfConcept Scale scores

(Piers & Harris,

1969) between obese

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21

and normal weight children in Grades 3 through 8. They


reported no interaction among weight,
Magill and Hurlbut

grade,

or sex.

(1986) measured the self-concept of

children age 13 to 18 with cerebral palsy. No significant


differences were found between the handicapped and the
nonhandicapped children. However,

a significant interaction

was found between sex and disability, with the handicapped


females scoring lower than the handicapped males.
verse was found in the healthy children.

The re

No significant

differences were found between sexes on overall self-concept


(Magill & Hurlbut,

1986).

The Piers-Harris Children's Self-Concept Scale (Piers 6


Harris,

1969) was utilized to assess the self-concept scores

of black obese children in Grades 4 through 12 (Kaplan &


Wadden,
normal

1986). The self-concept scores were all within


range and were not affected by age or sex. The re

searchers concluded that the consequences of childhood


obesity may be less harmful psychosocially than formerly
presumed.

The promise of enhanced self-concept would fail to

motivate weight

loss in many children. While obesity was not

associated with impaired self-concept,

leanness was a ssoci

ated with enhanced self-worth (Kaplan S Wadden,


Cadman,

Boyle,

1986).

S z a t ma ri, and Offord (1987) ascertained

that children with chronic health problems are at signifi


cantly greater risk for psychiatric problems, social and
school

adjustment problems, neuroses,

disorders than their healthy peers.

and attention deficit

The authors studied

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22

children age 4 to 16 who had a chronic illness or disability


and found an association between chronic health problems and
mental health problems,
term disability.

especially in children with a long

They suggested that poor social adjustment

and school problems may include poor self-concept and may be


precursors of psychiatric problems.
Children with sickle cell disease were the focus of a
self-concept study conducted by Kumar,
Haywood (1976).

P o w a r s , Allen,

and

The researchers utilized the Piers-Harris

Children's Self-Concept Scale (Piers & Harris,

1969) and

ascertained that children with sickle cell disease were not


different than the control group on the personal,

social,

and total adjustment scores. The children with sickle cell


disease did tend to withdraw and had lower level social
skills than the control group.

Interestingly,

the children

with sickle cell disease showed considerably less anxiety


than the control group (Kumar et a l ., 1976).
Psychosocial Responses to Childhood Cancer
Mattson (1972) identified malaise,
symptoms,

pain, physical

reasons for illness, hospitalization,

procedures,

painful

and specific stressors related to the illness as

frequent causes of psychological

stress associated with

chronic illness. Children with cancer have been reported as


missing more school than their healthy peers.

Psychosocial

problems have been associated with this increase in school


absences
(1983)

(Weitzman, Walker,

& Gortmaker,

emphasized this point,

1986).

Klopovich

stating that children with

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23

cancer continue to miss school


apparent physical

even years after there is no

cause. Older children and adolescents are

at higher risk for developing school phobias than young


children (Lansky,

Lowman, Vats,

& Guylay,

Early research on psychosocial

1975).

problems in childhood

cancer was conducted in suboptimal psychological

conditions.

Mo r e recent research has shown that children who have open


communication and appropriate information about their di ag
nosis and prognosis have better long-term psychosocial
adjustment.

They have a higher level of self-regard and

remain closer to family members. Wi th a more open approach


to children and families currently being employed,
of early studies of psychosocial

adjustment to childhood

cancer may not apply to children diagnosed today


Copeland,

results

(Micheal

&

1987).

Chronic stressors of childhood cancer,


gain or loss,

school

ment related pain,

absences,

separation from peers,

chronic nausea,

act to impact psychosocial

such as weight

and alopecia,

adjustment.

treat

all in te r

Demographic variables

may explain a small amount of variance in psychosocial


adjustment of kids with cancer.
sized that social

Varni et a l . (1994) h y p o t h e

environment variables might explain some

of the variance in adaptation of children with cancer.


study,

lasting 4 years,

Their

included subjects ranging in age

from 8 to 13 years. M u l t ipl e regression analyses revealed


that children with de creased perceived social

support had an

increased risk for psychological adjustment problems.

The

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24
researchers concluded that social

skills training might

increase social competence, which in turn will decrease


adjustment problems.

Social

competence is viewed as a p r e

ventative intervention, w h ich increases over time

(Varni et

al., 1994).
Brunquell and Hall

(1982)

researched children age 6 to

10 years of age who supposedly were unaware of the fatal


nature of their cancer.

These children showed clear evidence

of an awareness of the seriousness of their illness.

The

fatally ill child showed excessive anxiety and preoccupation


with threats to body integrity,

and made overt references to

death.
Spinetta

(1981) found that the child's level

of anxiety

and feelings of isolation were directly related to family


patterns of communication.

Children with cancer who come

from families with open communication have a better selfconcept,

are less defensive,

and have a closer relationship

with family members.


Koocher et a l . (1980) have performed extensive studies
of children with cancer.

They have found that developmental

disruptions engendered by cancer treatment are more marked


and more persistent when they occur in middle childhood and
adolescence,

as compared to infancy.

These researchers

studied former pediatric oncology clients and found that 59%


had lingering psychosocial

problems.

Children who were

younger at diagnosis had fewer adjustment problems.


of treatment was not found to be important,

Duration

but age at

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25

diagnosis and time since diagnosis were significant factors.


Depression,

anxiety, and poor self-concept were experienced

by a significant number of children who survive pediatric


cancer experiences

(Koocher

Research was conducted

et a l ., 1980).
by Kimsey (1990) to investigate

parent's response to a cancer diagnosis in their child and


to assess the relationship of these variables to the psycho
logical adaptation of the child during diagnosis and treat
ment. Results indicate that diagnosis and prognosis are not
related to parent or child adjustment to the disease.
child's psychological

The

functioning before diagnosis is the

best index of their adjustment to the disease process.


Fergusson (1976) studied 18

subjects who had been treated

for cancer between the ages

of 2 to 5 years. This

researcher

concluded that psychologic damage does not necessarily


follow treatment for cancer in early childhood.

Children who

had their diagnosis fully discussed with them were function


ally normal.

Factors identified as contributing to the

child's well being during hospitalization and treatment for


cancer included the parent-child relationship,
family structure,
(Fergusson,

changes in

and interaction with the health care team

1976).

Hymovich and Roehnert

(1989) report that survivors of

childhood cancer with severe medical


poorer self-concept,
symptomatology,

effects may have a

lower popularity, more depressive

and more external

locus of control than

survivors with mild or moderate late medical

effects. Girls

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26

exhibit greater anxiety and concern than boys about their


physical appearance. Factors associated with better ps ycho
social adjustment for long-term survivors of childhood
cancer include younger age at onset,
diagnosis,
relapse,

longer time since

shorter treatment duration,

remission without

early knowledge of the disease,

communication,

open and supportive

and higher social maturity.

Resources gen er

ally considered to enhance a long-term survivor's ability to


resist detrimental
adaptive individual

effects of childhood cancer include


coping skills and an emotionally sup

portive social network.

Development of effective interven

tion programs is hindered by the lack of research investi


gating the psychosocial
diagnosis

consequences of a childhood cancer

(Hymovich & Roehnert,

Feelings of anxiety,

1989).

depression,

fear,

and helplessness

often accompany the diagnosis of childhood cancer.

Survival

rates have drastically improved while the impact of the


diagnosis has not. The impact of childhood cancer may be
physical

or psychological

pacts may be obvious,

or both. While the physical

the psychological

im

impact may be more

subtle (Hockenberry et a l ., 1990). Bossert and Martinson


(1990) utilized kinetic family drawings to determine the
impact of cancer on the family from the perception of the
child with cancer. The authors found a trend in type of
cancer,

sex, and status of cancer.

age or in family dynamics.

They found no trend in

The scores of children with

leukemia were significantly lower on communication and

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27

self-image,
emotional

while children with solid tumors scored lower on

tone and had poorer scores over time. W h e n com par

ing cohesive families to fragmented families,

no trends were

identified.

The authors suggest that, f ro m the child's

perspective,

their family's attitudes and emotions become

more regular as time from diagnosis increases


Martinson,

(Bossert S

1990).

Neff and Beardslee


children with cancer.

(1990) studied body knowledge of

They hypothesized that anticipatory

anxiety is a conditioned behavioral


invasive procedures.

response to repeated

The authors found that fatally ill

children had significantly higher levels of anxiety.


comparison was made of children with cancer,
problems,

and healthy school age children.

orthopedic

Children with

cancer were found to have more knowledge about body func


tioning than the other groups. Children w i t h cancer also
indicated significantly m o re bodily concerns.

It was con

cluded that body integrity concerns are m o re likely to be


expressed when a child anticipates,
ed with,

or is actually c o nf ron t

a stressor that has the potential

to violate body

integrity.
Gregory,

Parker,

returning to school
cancer.

and Craft

(1994) studied 14 children

after extended absence for treatment of

The researchers utilized a control group of healthy

children and a group of 11 siblings of children with cancer.


Behavioral

rating scores showed no significant differences

in socialization,

emotional behavior,

performance.

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28

adaptation,

or learning disabilities.

Teachers anticipated

many problems when the child with cancer returned to school,


but few problems were actually experienced.
cited support from staff,
and physicians,

The researchers

including nurses, social workers,

as being invaluable as evidenced by the ease

with which the children with cancer reintegrated with their


peers.
Both diagnosis and treatment of cancer are sources of
stress to the client with cancer. Wi th the reduction of
therapy toxicities,

psychosocial

difficulties may become one

of the major long-term complications of treatment. R e


searchers studying survivors of Hodgkin's disease found that
37% suffered from persistent energy loss.

The remainder of

the subjects reported requiring 12 to 16 months for energy


levels to return to normal.
of the sample.

Depression was indicated in 18%

The inability to per fo rm usual activities and

the resulting loss of social

contact clearly undermined

self-concept and generated feelings of guilt in a small


percentage of the sample (Fobair et a l ., 1986).
Van Dongen-Melman and Sanders-Woudstra (1986) conducted
an extensive review of the literature pertaining to the
psychosocial

aspects of childhood cancer.

Their review

indicated that the more complex the cancer treatment regimen


the more likely it is to interfere with psychosocial
bilitation.

reha

The child w ith cancer experiences greater a n x i

ety with the progression of the disease and with every


clinic visit.

This results in greater susceptibility to

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29

psychosocial problems. Recurrent procedures pose problems in


psychosocial adjustment, which may include such symptoms as
insomnia, nightmares,

anorexia, withdrawal,

Factors that seem related to optimal

and depression.

long-term psychosocial

adjustment include a short treatment course, continuous


remission without relapse,

early knowledge of the disease,

supportive and open communication,

and age at disease onset.

The researchers point out that limited attention has been


given to the emotional aspects of living with the diagnosis
of cancer.
Social

Support and Health

Social support appears to enhance effective coping with


stressors.

Social support may buffer stress by intervening

between the stressor and the outcome by weakening a stress


or perceived threat appraisal.

It may play a role in inter

vention between the threat appraisal

and outcome by altering

the reaction to the perceived threat through offering a


solution or decreasing the importance of the threat

(McNett,

1987).
Families appear to be the principal

environmental

source of social support for children (Boyce,

1985).

Boyce

defines childhood social support as those resources provided


to the child through intimate relationships and social
interactions. There is limited information regarding the
origin and character of the social support that children
receive and provide, or of the evolution of supportive
family interactions.

Childhood family attachment is

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30

essential

in the evolution of social support. Development of

attachment to the social environment is crucial

in order for

the child to fulfill a need for stability and develop a


capacity for successful

social

interactions.

Stressors act

on the health of a child through their ability to undermine


the child's sense of stability or permanence.

Social support

may function to promote some sense of permanence and c o n t i


nuity, which are representative of the meaning of social
support in a child's life (Boyce,
Woodbury

1985).

(1992) examined the characteristics and e f

fects of children's social support in relation to sel f


esteem and behavior problems.

Data suggest that children who

are less stressed have higher self-esteem and fewer behavior


problems.

Social support has a tendency to enhance a dju st

ment over time for children with both high and low levels of
stress. Results also indicate that satisfaction and social
support act as a buffer against poor adjustment to stressful
life circumstance in 13 to 14 year old subjects.
support does show developmental

Social

change and is essential

to

the maintenance of a child's emotional health (Woodbury,


1992).
Marital

status and social

support in relation to c h i l d

ren's self-esteem was studied by Read

(1991). The Piers-

Harris C h i l d r e n s Self-Concept Scale was used to compare


levels of self-esteem of children, age 8 to 10 years, whose
parents had divorced versus self-esteem of children from
traditional

two-parent families.

The researchers found that

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31

the level

of social support perceived by the child was

proportional

to the level of the child's self-esteem.

perceived higher intrapersonal

Girls

social support than boys.

longer parents had been divorced,

The

the higher the child's

self-esteem.
Support systems of college students were studied by
Parish and Parish (1991). The researchers were concerned
with the impact of changes in family configurations and
support systems,

occurring during school age and a d o l e s

cence, and their effects on support systems and self-concept


in later college years. Results showed that college students
whose parents divorced were significantly more likely to
encounter support system failures including parental h o s t i l
ity, perceived lack of caring,
of teacher concern,

inadequate supervision,

and increased financial hardship.

lack
These

support system failures were associated with decreased selfconcept and decreased social

skills

(Parish & Parish,

1991).

It has been determined that the quality of life of


children with cancer is influenced to a great extent by
family members,
policies.

health care providers,

and health care

This influence comes from the availability of

supportive resources for the child with cancer.


influence quality of life include internal
as how the child relates to the self;

Factors that

environment,

immediate environment,

including significant others and health care providers;


institutional

environment,

such

such as public and social

and

sys

tems .

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32

In a study by Chekryn,

Deegan,

and Reid (1986),

chi l

dren with cancer identified socialization with peers as what


they liked best about school.
the most common fear,
tal source of support.

Although peer rejection was

classmates were viewed as a fundamen


Play with peers provided an opportu

nity for stress release and respite from the sick role. The
results of the study indicate that a positive school

experi

ence can provide the child with a sense of accomplishment


and social acceptability,

strengthening self-esteem,

decreasing maladaptive emotional


In a study of maternal
fants,

Capuzzi

and

responses to cancer.

attachment to handicapped i n

(1989) found that the stressor of having a

handicapped infant interferes with the development of m a t e r


nal attachment.

Social support facilitates attachment by

reducing the stress of having a handicapped infant.

Capuzzi

suggested that social support plays an important role in


buffering the stressors of having a handicapped child.
Therefore,

social

support systems should be promoted and

increased.
People wi th cancer often experience a loss of a sense
of self.
a degree,
1982).

This perceived loss can be relieved or lessened,


by support from significant others

(Maxwell,

Studies of cancer patients suggest that social

port is associated with better psychosocial


the illness

(Mishel & Braden,

1987).

sup

adjustment to

It has been postulated

that the uncertainties and fears associated with cancer


generate the need for social

to

support in oncology patients.

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33

Further,

adequate communication with significant others

facilitates the cancer patient's ability to deal with the


diagnosis and treatment of cancer. Findings of the study
conducted by Mishel and Braden support the proposition that
social support functions change over time. Also, social
support influences varying aspects of the uncertainty of the
cancer diagnosis.

The authors conclude that social support

may have a direct as well as indirect influence on adjust


ment to life with a chronic illness.
Stewart

(1989) reviewed social support instruments

created by nurse investigators. Measures of structure,


function,

and nature of social support were found to be

common to all instruments reviewed.

The three sources of

social support most consistently measured were family,


friend,

and spouse.

Burnout and social support were studied in family


caregivers

(Lindgren,

1990).

identified as a personal

Social support was conceptually

resource for coping with the stress

of giving care and is negatively related to the degree of


burnout experienced.

Study participants who felt they re

ceived social support reported a sense of accomplishment.


This is reinforced by commendations from others that enhance
the individual's sense of self-esteem.
Riegel

(1989) determined that effective social support

is directly and positively related to positive


tion;

self-evalua

increased self-concept; mastery over the environment;

and enhanced feelings of love, worth, importance,

and

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34

esteem.

Social support that has positive effects on well

being and adjustment to chronic illness may actually be


serving as a buffer to the stressors of the illness.

Social

support may lead to negative effects and feelings when the


receiver of the support fears inadequacy,
loss of freedom.

indebtedness,

or

These feelings may in turn lead to a p e r

ceived loss of competence and decreased self-concept.


support is a major factor influencing self-concept,
ceived functioning capacity, mood,

Social

per

and adjustment to life

with a chronic illness ( R i e g e l , 1989).

It is concluded that

the quality of social support is a major determinant of an


individual's adjustment to life with a chronic illness.
Quality of social support is affected by chronic ill
ness

(Tilden & Weinert,

1987).

The chronically ill person

may be unable to reciprocate the received support.


lead to strain on the social network.
is stigmatizing or anxiety ridden,

If the chronic illness

the social support n e t

work may eventually dilute or withdraw,

resulting in social

isolation or impaired social interaction.


ing to social

This may

Factors c on tribut

isolation include altered physical appearance,

altered mental state, altered states of wellness,

d e vel op

mental delays or changes,

resources.

Ineffective social
dysfunctional
iors.

and inadequate personal

exchange may include social discomfort,

communication,

and inappropriate social b e h a v

Self-concept disturbances and major emotional d i s o r

ders are common factors to both social


paired social

isolation and im

interaction (Tilden & Weinert,

1987).

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35

Cherry

(1991) compared self-esteem of adolescents wit h

cerebral palsy or spina bifida to the self-esteem of ablebodied adolescents age 13-19 years. The author identified
other variables that may correlate with self-esteem.

Results

indicated no significant differences between the two groups


for self-esteem or for social support from family.

The able-

bodied adolescent perceived higher levels of social support


from peers and perceived larger social

support networks.

The

able-bodied adolescent participated more frequently in


shared peer activities. Multiple regression analysis re
vealed four factors that accounted for 77.4% of self- est ee m
variance in the physically disabled adolescent group.
factors were social support from peers,
from father,
pendence.

team sport participation,

reflected appraisals
and functional

included social

support from friends,

These factors

social support from

and frequency of attending a school

athletic event.

The researcher concluded that perceived social


peers,

inde

Three factors accounted for 54.8% of the variance

in self-esteem for the able-bodied adolescent.

family,

These

support

from

shared activities with peers related to self-esteem,

and family influences on self-esteem were important.


Chronic illness places the individual
social

isolation or impairment.

at high risk for

Social support is often

strained or disrupted and may even disintegrate under the


stressors of chronic illness and its treatment.

The effects

of chronic illness may reduce the individual's ability to


maintain,

develop,

or reciprocate social support.

Lowered

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36

self-concept,

depression,

and dependency may result.

It is

suggested that nursing intervention should focus on finding


new methods of reciprocation to prevent deterioration of the
social support network and to promote a more positive selfconcept

(Tilden & Weinert,

1987).

Noll, B o k o w s k i , Davies, Koontz,


examined the psychosocial

and Kulkarni

(1993)

adaptations of children age 11 to

18 years who were primarily off treatment

for cancer.

The

researchers used a variety of sources for information,


multiple standardized measures,

and matched controls.

The

subjects were found to have a reputation of being socially


isolated,

however,

friendship,

no differences were found in popularity,

self-concept,

or loneliness.

The researchers

extended the study longitudinally to ascertain if there were


long-term problems with peer relationships and to determine
whether the children with cancer showed differences in
loneliness,

depression,

and self-concept.

Results suggested

that whether the child was receiving treatment or had com


pleted treatment for cancer had little effect on social
reputation,

popularity,

friendships,

or self-concept.

The

study indicates that adolescents with cancer may experience


social
overall

isolation,

popularity,

self-concept.
social

but the isolation has minimal


friendships,

effect on

loneliness, depression,

and

Further research is suggested in the area of

competence and social support of children with can

cer .

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37

Self-Concept and Childhood Cancer


Utilizing the Piers-Harris Children's Self-Concept
Scale (Piers & Harris,

1969),

40 pediatric oncology clients

were studied by Carr-Gregg, White, Hughes,

and Vowels

(198-

5). Healthy children were matched with pediatric oncology


clients for age, sex, race, and socioeconomic status. R e
sults indicated significant relationships between selfconcept and family adjustment and support. Almost 75% of the
pediatric oncology clients scored below the published norms
on the self-concept tool

(Carr-Gregg et a l ., 1985). Carr-

Gregg and White (1987) studied self-concept in relation to


disease type among adolescents with cancer. Their results
suggested that adolescents with solid tumors have a poorer
self-concept than those adolescents with leukemia.
A study by South (1988) compared the self-concept of
school

age survivors of acute leukemia and the self-concept

of healthy school

age children.

Instruments utilized were an

investigator constructed demographic tool and the PiersHarris Children's Self-Concept Scale (Piers & Harris,

1969).

One-way analysis of variance revealed a significant differ


ence in self-concept between the two groups.

Significant

differences were also found between the two groups on the


Physical Appearance and Attributes subscale and the Intel
lectual and School Status subscale of the self-concept tool.
Twenty-two subjects were included in the study. No attempt
was made to measure or control developmental stage, previous
adaptive capacity,

the meaning of the illness to the child

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38

and family,

the parent-child relationship,

reaction to changes in equilibrium.


knowledge concerning diagnosis,

and the child's

The child's

level of

disease state, and prognosis

was not assessed.


Benson (1987) studied children ages 7 to 18 who were
attending a pediatric oncology camp for the first time.
Fourteen subjects were pretested and posttested utilizing
the Piers-Harris C h i l d r e n s Self-Concept Scale (1969) and
kinetic family drawings,

t tests showed no significant

differences in self-concept.

Since self-concept is relative

ly stable and does not change over a short period of time,


this finding is to be expected.
Self-concepts of school

age children with leukemia were

compared to self-concepts of healthy school age children by


Scungio (1981).

It was ascertained that children with leuke

mia reported significantly lower self-concepts than the


healthy school

age children.

Burns and Zweig (1980) studied self-concept of well


children and children with cancer.

The sample consisted of

54 children with oncological disorders and 115 healthy


school age children ranging in age from 3 to 12 years. The
mean self-concept scores of the children with cancer did not
differ significantly from the scores of the healthy chil
dren. The researchers recognized the possibility that the
child with cancer may deny a poor self-concept.
with cancer viewed themselves as friendlier,

The children

possibly to

overcompensate for feelings of social isolation.

It was also

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39

found that dying children rely strongly on such coping


mechanisms as denial,

repression,

and hope,

and can use

those mechanisms to maintain equilibrium between ego ideal


and a more realistic self-concept.

Burns and Zweig stressed

the importance of identifying the psychosocial

effects of a

chronic illness so that appropriate intervention can be


provided.
Summary
The research cited provided the background for this
study.

The literature was placed within the categories of

self-concept in chronic illness,

psychosocial

responses to

childhood cancer, social support and self-concept in rela


tion to health and well being,
cancer.
social

and self-concept in childhood

There were no studies of relationships between


support and self-concept in children with chronic

i 1 In e s s .
Variations in research findings may be due to v ari a
tions in methods of data collection,

such as use of c on

trols, sources of information, use of nonstandardized m e a


sures,

and problems with observer bias. Very little data

could be found relevant to the adjustment of children with


chronic illness within their social peer group.
The review of research indicates that social support
may be an especially vulnerable area for children with
cancer

(Koocher et a l ., 1980). Many of the stressors a s s o c i

ated with pediatric cancer develop in the structure of

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40

coping w i th peer pressure and the social consequences of


having a chronic illness

(LaGreca,

1990).

Children with cancer are dealt with more openly today,


so that early research in the areas of psychosocial

ad jus t

ment may no longer be valid when applied to children cur


rently diagnosed with cancer.
ing psychological
ric oncology,

Studies previously invest iga t

factors and stress in relation to p ed i a t

and studies of social support, have had poor

methodological

rigor, so that conclusions based on results

of early studies must remain imprecise and general.


fore,

T here

limited evidence is actually available concerning

psychosocial

factors associated with the occurrence and

subsequent treatment of cancer.

There is a paucity of re

search specifically related to self-concept and social


support in children with a chronic illness.

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Chapter III
Methodoloqy
The purpose of this research was to ascertain if there
is a relationship between self-concept and social support of
school age children with leukemia.
the design of the study,

In the following chapter,

instrumentation,

procedure will be described.

subjects,

and

The method of data analysis and

limitations of the research will also be presented.


Design
This study is descriptive in design.

The variables

included in the research are stage of antileukemia therapy,


age, gender,

race, social support as measured by the Person

al Resource Questionnaire,
Weinert,

1985),

Part 2 (PRQ 85)

(Brandt &

and self-concept as measured by Piers Harris

Children's Self-Concept Scale

(PHCSCS)

(Piers S Harris,

1969).
Instrumentation
A demographic and information questionnaire was devel
oped by the researcher in order to obtain factual informa
tion concerning the diagnosis,

treatment,

and stage of therapy for each subject.

age,

race, gender,

The demographic

questionnaire also served as the consent form and was signed


by at least one parent and the child when completed.

41

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42
The PRQ 85 Part 2 was utilized to measure social s u p
port as perceived by each subject.

The PRQ was originally

developed by Brandt and Weinert in 1981. Following extensive


testing and modification,

the PRQ 85 has evolved as the

current version of the tool. The tool consists of a twopart,

self-administered questionnaire.

Part 1 describes

situational support in the context of life situations.


2 describes perceived social

support consisting of a five-

factor structure of intimacy,


ce, worth,

Part

social

integration,

nurturan-

and assistance.

Part 2 of the PRQ 85 was utilized for the present study


and consists of 25 items on a 7 point Likert scale.

The PRQ

85 Part 2 requires approximately 10 min to complete.


ble scores range from 25 to 175.

Scores greater than 150

indicate higher levels of perceived social support


& Tilden,

P o s si

(Weinert

1990).

Weinert and Tilden (1990)

report internal

consistency

coefficients ranging from 0.87 to 0.90 for the total social


support scale.

Subscale reliability coefficients have ranged

from 0.70 to 0.88.

Total scale to subscale correlations

range from 0.70 to 0.81

(Weinert,

1987).

Construct validity information was obtained with corre


lations between the PRQ 85 and the social support subscale
of the Cost and Reciprocity Index (Tilden S Galyen,

1987).

Correlation coefficients ranged from 0.53 to 0.58,


indicating that both tools are measuring the same construct
yet are not highly redundant

(Weinert & Tilden,

1990).

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43

Royeen (1985) studied the use of Likert scaling with


children.

Likert scaling was found to be the most widely

used and recognized as the easiest and most reliable tec h


nique for data collection.

Children reported less anxiety

during administration of Likert scaling instruments when


they were told it was a game and not a test.

Rephrasing

items from statement to question format made them more


comprehensible for children. Most items were clearly u n d e r
stood by the children unless the item had two parts such as:
Does it bother you to have your socks pulled up, after they
have fallen down? Royeen suggested that all items have only
one straightforward concept with no dependent clauses.

It

was concluded that Likert scaling is appropriate for use in


children. The PRQ 85 has been chiefly administered to
adults, but has been utilized in adolescents.
PRQ 85 measures the theoretical

Because the

concept of social support,

as well as its multidimensionality,

it was deemed a p p rop ri

ate for the purpose of this study.


The PHCSCS

(Piers & Harris,

1969) was utilized to

measure self-concept of each subject.

The PHCSCS is a self-

report instrument that consists of 80 items.

It requires

about 20 min to complete and is appropriate for a wide age


range (Piers & Harris,

1969). The PHCSCS provides a total

self-concept score as well as subscores for:


(b) intellectual
and attributes,

and school

status,

(d) anxiety,

ness and satisfaction (Piers,

(a) behavior,

(c) physical

(e) popularity,

appearance

and (f) h a p p i

1984).

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44
M uch of the reliability of the PHCSCS is based on the
original standardization study.

Piers

(1984) obtained i nter

nal consistency coefficient scores ranging from 0.88 to 0.93


using the KR-20 formula on the total scores of a normative
sample of 6th and 10th graders.

Lefley

(1974) utilized the

PHCSCS with native Americans ranging in age from 7 to 14


years.

Split-half reliability,

formula,
Rogers

using the Spearman-Brown

gave a reliability coefficient of 0.91.

Smith and

(1978) administered the PHCSCS to subjects age 6 to

12 years who had learning disabilities.

They reported an

alpha coefficient of 0.89 for the total scores obtained.


Reliability coefficients for the six subscales were
based on the standardization study sample of children in
Grades 4 through 12 and a sample of children from three
psychiatric clinics. The alpha coefficients ranged from 0.73
to 0.81

for each of the subscales, while the coefficient for

the total score was 0.90.


to be 0.72,

0.71,

Stability coefficients were found

and 0.72 over a 4-month period

(Piers,

1984) .
Franklin,

Duley, Rousseau,

and Sabers

(1981) studied

convergent and discriminant validity of the PHCSCS by c o m


paring it to the Self-Esteem Inventory

(Coopersmith,

1967).

Convergent validity was evidenced by a correlation co e f f i


cient of 0.78. Multiple correlations produced coefficients
not exceeding 0.25 between self-concept and academic a c h i e v
ement,

socioeconomic status,

ethnic background,

special

grade placement,

education placement,
sex, and age variables.

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45

Possible intervening variables were identified through


literature review and logic. The variables considered prior
to hypotheses testing were age,

race, and sex. The effects

of these variables have been evaluated to identify interac


tion patterns that reflect valid group differences on the
PHCSCS. The sample on which the PHCSCS was standardized did
not indicate differences in self-concept according to age.
The standardization sample included subjects in Grades 4, 6,
8, 10, and 12 (Piers & Harris,

1964). Multiple studies

utilizing the PHCSCS have reported no significant d iff erenc


es due to gender
Ketcham & Snyder,
by Bentler

(Crase, Foss,

& Colbert,

1977; Piers & Harris,

1981; Devoe,

1964).

1977;

In a review

(1972), no significant sex or grade differences

in means were identified.

Bentler states that reliability

and validity are present and sufficient,

and recommends the

PHCSCS for use in research.


The PHCSCS is simple to administer and score. When
administered individually or in a group,
items should be read aloud for clarity.
defining terms are also given.

the directions and


Instructions for

Each item has been written so

that it is scored in the direction of high self-concept.

The

key for scoring each item is included in the test manual.


Norms and stanine scores are given, which take into account
the negative skewness,

or the tendency of the general p o p u

lation to respond in a generally positive fashion.


The items on the PHCSCS are constructed to reflect the
concerns children have about themselves.

Piers

(1984) states

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46
that variability of scores decreases as grade level in cre as
es. Piers further reports that all high scores cannot be
assumed to reflect true positive self-attitudes,

but it can

be assumed that low scores reflect true negative self -at ti


tudes .
Subjects
The sample for this research consisted of children,
8 to 12 years, who had a diagnosis of leukemia.

age

All pa r t i c i

pants were able to read and write and were physically able
to complete the instruments.
or mental

limitations,

Children with obvious physical

other than those related to cancer

diagnosis and treatment,

were excluded from the study.

Participants were chosen by convenience at two pediatric


oncology treatment centers in the southeastern United
States. There was no random selection of subjects.

Children

were contacted at the time of their regular clinic a p poi nt


ment. All

children who met the inclusion criteria,

and who

had a parent available to give consent, were asked to p a r


ticipate in the research.
Setting
Data collection for this study took place at two p e d i
atric oncology/hematology clinics.

The researcher attended

outpatient clinics in an effort to identify those children


eligible for the study.
identifying subjects.

Clinic receptionists assisted in

Subjects and their parent or guardian

met the researcher or interviewer in an examination room or

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47

the patient interview room. A parent or guardian was present


at all times, in addition to the interviewer.
Procedure for Data Collection
In order to safeguard the human rights of the p a rt ici
pants in the research,

the researcher secured permission to

conduct the research from the Institutional Review Board of


the University of Alabama at Birmingham.

Writt en approval

to enter the agencies and seek the participation of subjects


was obtained from the appropriate administrators.

The p h y s i

cians caring for children with cancer at the major medical


centers were contacted by formal

letter and telephone r e

questing permission to seek participation of their clients


in the research.

These physicians signed permission forms

for their clients to participate.


A letter of information and consent/assent was given to
all children and their parents at the time of the regular
clinic visit.

Assent was obtained from each child who p a r

ticipated in the study,

and informed consent was obtained

from at least one parent of each participant.

The researcher

attended clinic and gave consent/assent forms to all on colo


gy clients with leukemia who met inclusion criteria. All
clients who met inclusion criteria and agreed to participate
were included in the research.
Children who agreed to participate,
agreed to allow participation,
Harris,

and whose parents

completed the PHCSCS (Piers &

1969) and the PRQ 85 Part 2 (Brandt & Weinert,

1985)

in a parent interview room. The parent accompanying the

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48

child completed the demographic and information q u e s tio n


naire developed by the researcher.

Specific guidelines were

developed for approaching children and administering the


research tools so that the procedure did not vary with each
child.
The researcher scored the PHCSCS and the PRQ 85 Part 2,
and coded the demographic information.

No other individual

reviewed the information or was able to identify the s u b


jects.

In this way confidentiality and anonymity of subjects

were maintained.

All data are reported as group data so that

no individual score can be identified.


to withdraw,

Children were allowed

or be withdrawn by a parent or guardian,

point in the study until

at any

completion of the instruments and

questionnaire.
Analysis
The statistical hypotheses are stated in the null form:
(a) There will be no statistically significant relationship
between the total scores on the PHCSCS and the PRQ 85 Part 2
among school age children with leukemia,

and (b) there will

be no statistically significant relationship between the


subscale scores on the PHCSCS and the PRQ 85 Part 2 among
school

age children with leukemia.

Regression analyses were computed to ascertain if


significant relationships existed at the 0.05 level between
total

scores and subscale scores on the PHCSCS and the PRQ

85 Part 2 of school age children with leukemia.

Stepwise

multiple regression begins with no variables and adds

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variables one at a time. After adding each variable,

all

previously added variables are reevaluated for significance.


If a variable is considered that does not contribute signif
icantly to an increase in variance,
equation.

In this way,

it is removed from the

the unique significance of each

variable can be ascertained (Norusis,


predictive variables are considered;

1988). All potential


and the combination of

variables providing the most predictive power are selected


(Polit & Hungler,

1983).

The effects of a predictor variable

on a criterion variable can be isolated,

and fraudulent

influences can be controlled for by using stepwise multiple


regression.

Incremental variance accounted for by a set of

variables can also be investigated.


can be explained,

The more variance that

the stronger the findings and conclusions.

Limitations
The target population for this research is restrictive.
Therefore,

conclusions are limited to the specific p op ula

tion. The subjects for this study were selected by conve


nience rather than randomly selected. This also limited the
generalizability of the results.

Parents or guardians were

not separated from their children for the administration of


the research questionnaires.

The presence of the parent or

guardian may have influenced the child's responses.

Data

were self-reported and so may represent only what the s u b


ject is willing to report.

Present mood of the subject may

also affect responses.

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50

Summary
This chapter has examined the methodology of the p r e s
ent research. The design of the study,
subjects have been identified.
data analysis were presented,

instrumentation,

and

The procedure and methods of


as well as limitations of the

study.

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Chapter IV
Findings
The purpose of this study was to describe social sup
port and self-concept in school

age children with leukemia

and to ascertain the relationship between social support and


self-concept in school age children with leukemia.

Demo

graphic descriptions of the study sample and findings of the


social support scale and the self-concept scale are p r e s e n t
ed in this chapter.

The results of the correlation and

regression analyses are also presented.


Des cri pti on of Subjects
Subjects were predominately m al e (70.6%) with 41% being
White male and 29% being Black male.

Subjects ranged in age

from 8 to 12 years with a mean age of 10.2 years and a


standard deviation of 1.79 years. The majority of the s a m
ple,

or 82%, were diagnosed with acute lymphocytic leukemia.

The remaining 18% were diagnosed with T cell

leukemia.

Children who were off therapy constituted 41% of the sample,


while 24% of the subjects had relapsed at least once since
their original diagnosis.

Eighteen percent of the sample

were newly diagnosed and in the remission induction phase of


therapy.

An additional

18% of the subjects were more than 6

weeks into therapy and on maintenance regimens.

Subjects

attended one of two pediatric oncology treatment centers.


51

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52
Both centers were members of the Pediatric Oncology Group so
that all subjects were receiving similar treatment.

Demo

graphic description of the sample is represented in Table 1.


Table 1
Frequency Distribution of Subjects by Age, Race,

and Sex

Sex

Race

Female

Ma le

Black

White

Age

29.4

5.9

23.5

11.8

17.6

11.8

5.9

5.9

11.8

10

11.8

11.8

11

11.8

11.8

12

35.3

17.6

17.6

17

100.0

29.4

12

70.6

Total

0
11.8
0

0
2

11.8

17.6

17.6

41.2

10

58.8

Analysis of the Data


R esearch Q uestion 1 . What is the self-concept of school
age children with leukemia? The mean score for the selfconcept of the total sample was 63.6, with a standard d e v i a
tion of 15.03.

Two scores,

or 11.8%, were below the average

score stated by Piers and Harris


within the average range.

(1969).

Two scores were

The remaining 76.4% was above the

stated average score for self-concept.

Descriptive s t ati s

tics of the self-concept scores are displayed in Table 2.

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53

Descriptive statistics for the six subscale scores are also


presented in Table 2.
Table 2
Descriptive Statistics for Self-Concept Scores
Mdn

Mde

8.65

10

10

5.49

2.34

3-10

13.41

14

14

13.76

3.71

4-16

Popularity

8.94

4.43

2.11

4-12

Physical
appearance

10.41

12

13

9.88

3.14

4-13

Intelligence

14.24

16

16

12.19

3.49

4-17

Anxiety

10.65

11

11

8.62

2.94

3-14

Total score

63.65

70

72

225.87

15.03

23-76

M
Happiness &
satisfaction
Behavior

Variance

SD

Range

Research Question 2. What is the social support of


school

age children with leukemia? The mean score for social

support of the sample was 146 with a standard deviation of


16.14.

Scores ranged from 88 to 162. Fifty-three percent of

the scores were considered moderate scores

(n = 9). The

remaining 47% of scores were in the high range. There were


no low range scores.

Therefore,

moderate to high social support.

all subjects perceived


The social support s t ati s

tics are given in Table 3.


R esearch Question 3 . Is there a relationship between
social support and self-concept of school

age children with

leukemia? Correlation coefficients were calculated using the


total score from the self-concept tool, the social support
scores,

and the six subscales of the self-concept tool. A

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54
statistically significant positive correlation was obtained
between the social support scores and the self-concept
scores (r = 0.545, p. = 0.012). Thus, as social support
scores increase,

the self-concept scores also increase.

Significant positive correlations were also obtained


between the social support scores and each of the selfconcept subscales of Happiness and Satisfaction,
Anxiety,

Popularity,

and Attributes.

Behavior,

Intelligence, and Physical Appearance

Regression analyses were obtained to examine

the relationships between the variables.

Perceived social

support was entered as Step 1 in the equation.


variable entered into the equation was sex,

The second

followed by

race. Age, stage, and diagnosis did not enter the equation.
The findings revealed that 30% of the variance of selfconcept was accounted for by the variable of social

support

(p < 0.05). Additionally 38% of the variance of self-concept


was accounted for by both social support and sex (p < 0.05).
By forcing race into the equation with sex and social s u p
port, 44.5% of the variance of self-concept could be a c
counted for (p < 0.05). The regression summary is reported
in Table 4.
To measure the strength of the linear relationship
between the observed values of self-concept and those p r e
dicted by the regression equation

(Goodness of Fit test), a

correlation coefficient was computed between observed and


predicted values. This coefficient was significant at the
0.05 1e v e l .

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55
In order to gain further insight into the relationship
between self-concept and social support,

regression analyses

were then computed for each of the six subscales of the


self-concept instrument.

Statistically significant results

were obtained for the subscales of Behavior,


and Satisfaction.

and Happiness

These results are displayed in Table 5 and

6.
Table 3
Frequencies for Social Support Scores
Scores

Raw score range

25-74

Low

75-149

Moderate

53

88-149

High

47

150-162

150-176

Table 4
Stepwise Multiple Regression Summary for
Self-Concept Total Scores
Step

Variable

Cumulative

SE of b

R 2__________ _________________________________

Social
Support

0.297

0.719

0.224

0.0068

Sex

0.378

-11.488

7.439

0.1465

________________________0.445_______
3
Race
-8.054
Note, b = slope

6.398________ 0.230

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56

Table 5
Stepwise Mult ipl e Regress ion for Behavior Subscale
Step

Variable

Cumulative
R

SE of b

Social
Support

0.398

0.183

0.053

0.0045

Sex

0.469

-2.482

1.776

0.1856

0.481

-0.823

1.527

0.5990

3
Race
N o t e . b = slope
Table 6

Stepwise Multiple Regression Summary for Happiness and


Satisfaction Subscale
Step

Variable

Cumulative
R

SE of b

Social
Support

0.266

0.112

0.035

0.0064

Sex

0.357

-1.933

1.147

0.1158

0.458

-1.536

0.986

0.1434

3
Race
N o t e . b = slope
Incidental Findings

Descriptive statistics were completed for the mean


self-concept scores by levels of perceived social

support.

It was noted that those subjects with higher levels of


social support had higher mean self-concept scores. One-way
analysis of variance revealed that these means were s i gni fi
cantly different at the 0.05 level.

This information is

summarized in Table 7.
Self-concept scores were grouped by stage of treatment.
r

Social support scores were also grouped by stage of treat


ment.

These results are shown in Table 8. The mean self-

concept and social support scores,

by stage of treatment.

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57

were not statistically significant at the 0.05 level.


interesting to note, however,

It was

that during the relapse stage

both the social support scores and the self-concept scores


were the lowest and were below the total mean scores.
Table 7
Descriptive Statistics for the M e a n Self-Concept Score by
Levels of Perceived Social Support
f

Scores
High (greater than 150)
Moderate

(75 to 149)

Low (less than 75)

sd

47

70.750

4.7434

53

57.333

18.3507

100

63.647

15.0289

0
17

Total

Mean

Table 8
Self-Concept and Social

Support by Stage of Therapy


Social support

Self -concept

Stage

Mean

SD

Induction

154.00

9.17

61.67

12.34

Maintenance

155.67

1.53

73.00

1.0

Off therapy

146.14

4.95

64.71

19.02

Relapse

132.75

29.86

56.25

14.57

Total

17

146.06

16.14

63. 65

15.03

M ean

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SD

In an attempt to further describe the sample,


as self-concept and social

support scores,

statistics were computed by age,

as well

descriptive

race, and sex of the s a m

ple. This information is given in Tables 9, 10, and 11.


Table 9
Self-Concept and Social Support by Race
Social support
Race

Self-concept

Mean

SD

Mean

SD

Black

141.29

23.87

64.86

14.51

White

10

149.40

7.31

62.80

16.10

Total

17

146.06

16.14

63.65

15.03

Table 10
Self-Concept and Social Support by Aqe
Social support
Age

Mean

Self-concept

SD

Mean

SD

152.80

4.21

73.00

2.24

139.50

2.12

49.50

37.48

10

156.00

0.0

72.00

11

155.00

9.89

56.50

12.02

12

139.14

22.69

61.86

12.99

17

146.06

16.14

63.65

15.03

Total

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59
Table 11
Self-Concept and Social

Support by Sex

Social
f

support

Self-concept

Mean

SD

135.4

26.78

64.00

14.35

Male

12

150.4

6.71

63.50

15.92

Total

17

146.1

16.14

63.65

15.03

Sex
Female

Mean

SD

Correlation coefficients were obtained for the selfconcept tool,

the social support tool, and the six self-

concept subscales with age,


ment.

race, sex, and stage of treat

Social support and stage of treatment were noted to be

significantly negatively correlated (r = -0.48, = 0.026).


No other statistically significant correlations were o b
tained with age,

race,

sex,

or stage of treatment.

Summary
Findings and analysis of data have been presented.
Demographic data were analyzed utilizing descriptive s tat i s
tics .
Measures of central
self-concept and social

tendency were used to analyze the


support scores.

Correlations were

utilized to ascertain if there was a relationship between


self-concept and social

support.

Stepwise multiple regres

sion was then chosen to determine the combination of v a r i


ables providing the most predictive power for the selfconcept of school

age children with leukemia.

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60

The research questions were addressed in this chapter.


The mean self-concept score was 63.65. Almost one third of
the scores fell below the mean.

The me an social support

score was found to be 146, with slightly less than one


fourth of scores falling below the mean.
Significant positive correlations existed between
social

support and the self-concept scores,

of the six subscale scores,

as well as each

and stage of therapy.

Stepwise

multiple regression revealed that nearly one half of the


variance in self-concept scores was accounted for by the
social
Age,

support variable when controlling for sex and race.

stage,

and diagnosis were not found to significantly

contribute to self-concept at the 0.05 level.

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Chapter V
Summa ry, Discussion, Conclusions.
Implications, and Recommendations

Summary
This chapter provides discussion of the findings of the
study in relation to the review of the literature.
are summarized from the analysis of data.

Findings

Conclusions and

implications are postulated along with recommendations for


future research.
The purpose of this study was to describe self-concept
and social support in school

age children with leukemia and

to ascertain if there is a relationship between self-concept


and social support in school age children with leukemia.

The

PHCSCS was administered to subjects to discover the selfconcept.

The PRQ 85 Part 2 was used to obtain a description

of perceived social support.

The PHCSCS,

the PRQ 85 Part 2,

and a demographic questionnaire developed by the researcher


were utilized to ascertain the relationship between social
support and self-concept.
The data were analyzed by computing descriptive s t a t i s
tics,

correlational matrices,

sis. The 0.05 level


analyses.

and stepwise regression a n a l y

of significance was u tilized for all

SPSS Studentware (Norusis,

1988) was used to

compute all statistics.


61

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62
Data analysis revealed the following findings:
1. The mean self-concept scores of school age children
with leukemia was 63.65 with a standard deviation of 15.03.
This mean score is above the average range of scores from 46
to 60, stated by Piers

(1984). The data revealed that 88% of

the subjects had average or above average self-concept


scores.
2. The mean social support scores of school age c h il
dren with leukemia was 146 with a standard deviation of
16.14.

All scores were within the moderate or high range for

perceived social support.

The mean of 146 is within the

moderate range reported by Brandt and Weinert

(1985).

3. A statistically significant relationship existed


between social support and self-concept scores of school age
children with leukemia.

Social support was associated with

29.7% of the variance in self-concept. A total

of 44.5% of

variance in self-concept was associated with social support


by controlling for sex and race.
4. Additionally a statistically significant relation
ship existed between social support and the Behavior s u b sc
ale and the Happiness and Satisfaction subscale scores on
the PHCSCS at the 0.05 level of significance.

Social support

was associated with 39.8% of variance in the Behavior s u b sc


ale of self-concept.
equation,

By controlling for race and sex in the

a total of 48.1% of the variance in self-concept

was accounted for.

Similarly, social support was associated

with 26.6% of the variance in the Happiness and Satisfaction

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63

subscale of self-concept.

By controlling for sex and race

bias, total variance accounted for by social support i n


creased to 45.8%.
Discussion
The findings of the present study are similar to s t u d
ies conducted by Carr-Gregg et a l ., (1985), Read (1991),
Parish and Parish (1991), Mishel and Braden (1987), Riegel
(1989), Cherry

(1991),

and Fobair et a l ., (1986).

Common to

all these studies is the conclusion that self-concept and


social support are related. Read concluded that the level of
social support is proportional

to the level of self-concept.

This finding is supported by the present research, which


concluded that social support is positively related to selfconcept and may be a determinant of an individual's a d jus t
ment to live with a chronic illness.
The findings of the present study also support the work
of Beddell et a l . (1977), who found a relationship between
self-concept and life stress in chronically ill children.
They concluded that environmental
nants of psychological well being.

influences were d e t erm i


Based on their findings

and the findings of the current study,


that environmental

influences,

it can be deduced

such as social support,

affects the self-concept of chronically ill children.


Varni et a l . (1994)

similarly studied children age 8 to

13 years and found that those with decreased social


had increased risk for psychological

support

adjustment problems.

Cadman et a l . (1987) also concluded that poor social

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64

adjustment and school problems include poor self-concept and


may be precursors of psychological
chronic illness.
study.

problems in children with

This finding is supported by the present

In the present sample decreased social

fact, does result in decreased self-concept,


indicator of further psychological

support,

in

which may be an

adjustment problems.

The present findings support research done by Woodbury


(1992).

Social support may buffer against poor adjustment to

the stressors of cancer as evidenced by higher self-concept


wit h higher levels of perceived social
wit h Wood bu ry and the present findings,

support.

Consistent

Parish and Parish

(1991) associated support system failures with decreased


self-concept.
The current study does not support the work of Noll et
a l . (1993),

who found that adolescents with cancer experi

ence social

isolation, but this isolation has little effect

on self-concept.

South (1988) found that children with

leukemia had significantly lower self-concept scores when


compared to a control group of healthy school age children.
While the present findings do indicate self-concept scores
to be w ith in the established norms,
to a control

group.

Similarly,

there was no comparison

Carr-Gregg et a l . (1985)

found that 75% of pediatric oncology clients scored below


the published norms for the PHCSCS

(Piers,

1984). However,

the present study found the maj ori ty of self-concept scores


to be wi thin the established norms for the self-concept
t o o l . This is consistent w i t h research conducted by Burns

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65

and Zweig

(1980) who found that the self-concept scores of

well children and children with cancer did not differ s i g


nificantly.
Van Dongen-Melman and Sanders Woudstra

(1986) found

that the more complex the treatment for cancer the more
likely children were to have psychosocial

problems.

Inter

estingly the present study indicates that self-concept and


social support may be related to the intensity of treatment,
because both self-concept and social support scores were
lowest for children in the intensive stages of beginning
therapy and those in relapse. This is an area in need of
further study.
Neuman's Systems model

(Neuman,

1989) provided an

excellent basis for guiding this research. The Neuman model


is congruent with pediatric oncology nursing. The pediatric
oncology client has unique needs and responses to stressors
that the nurse must identify,

assess,

and understand in

order to provide appropriate care so that the client can


achieve optimal wellness biologically as well as p syc hol og i
cally,

socioculturally,

d e v e l o p m e n t a l l y , and spiritually.

Neuman's Systems model suggests dynamic energy exchange


between the person and the environment. Nursing is concerned
with conserving energy to move toward wellness rather than
illness.

This model

can assist pediatric oncology nurses to

identify appropriate responses to stress related situations


and possible reactions of the client, such as decreasing
self-concept.

Nursing intervention can then be focused on

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66

decreasing stress factors and opposing conditions,


low perceived social support,

such as

that could affect optimal

client functioning and response to treatment.


Ultimately nursing must keep the client system rela
tively stable.

Stability is achieved through accurate a s

sessment of environmental stressors,

their effects,

and

responses of the client and in assisting the client to


adjust.

Stress occurs when situational demands surpass one's

ability to cope with certain events. Social support cushions


effects of stressors by lessening the severity of the re ac
tion to the stressor,

enhancing coping efforts,

and empower

ing the person to perceive the stress as less stressful.


The Neuman model has the ability to integrate health
related theories and concepts,
social support,

including self-concept and

and to elucidate the relationship of va ri

ables in nursing care. Nursing actions should include a s


sisting the pediatric oncology client in retaining,

at tain

ing, or maintaining optimal wellness through specific in ter


ventions aimed at reducing or relieving stressors.
tion should be based on client data,

Interven

relevant theory, and

research.
The concepts of prevention through intervention are
already used in oncology nursing,
Systems model

so that use of Neuman's

(Neuman, 1989) does not involve a major shift

in focus. The model

can provide theoretically valid and

consistent means to assess and intervene at the appropriate


level of prevention. With more open approaches used today,

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67

early studies of psychosocial

adjustment and consequences of

pediatric cancer and treatment may not apply to children


being treated today. Treatment for childhood leukemia does
not necessitate psychological damage.
Limitations
Conclusions may not be generalized beyond the sample
because a sample of convenience was utilized and because of
the small sample size.

It was difficult to recruit subjects

mainly due to small total potential subjects available.

The

average age of the child with acute lymphocytic leukemia is


2-9 years. Adolescents are more commonly affected by acute
nonlymphocytic leukemia. Therefore the pool of potential
subjects was severely limited.
about 3 years.

Data collection continued for

Despite small sample size, adequate power

was shown (0.89).


Conclusions
The results of the research show that school

age ch il

dren with leukemia with low levels of perceived social


support are significantly more likely to have low selfconcept in comparison to children with higher perceived
social support. For the present sample the following conclu
sions can be made:

(a) Perceived social support of school

age children with leukemia is moderate to high;

(b) reported

self-concept of school age children with leukemia is average


to high;

(c) there is a strong positive relationship between

social support and self-concept in school age children with


leukemia;

(d) if race and sex are controlled for, social

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68

support can account for nearly one half of the variance in


self-concept;

and (e) stage of therapy and age of subject

does not significantly impact self-concept.


Implications
Clinical

implications emerging and supported by this

research include:
1. Client and family teaching should include strategies
for dealing with disease specific social
2. Social

situations.

concerns of children with cancer can be

recognized early,

before they interfere with treatment or

future psychosocial

adaptation.

3. Positive and effective coping strategies should be


identified and reinforced from the point of diagnosis and
initiation of treatment.
4. Crisis points,
relapse of disease,

such as remission induction and

can be anticipated.

Psychosocial

inter

vention efforts can be intensified in preparation for these


crisis points.
5. Children at increased risk for psychosocial problems
should be identified,

and intense attention should be

focused on those children.


6. Methods of promoting social support of the child
with cancer should be identified,

including interventions

through community education.


Recommendations
The following recommendations are submitted for further
study based on the findings,

conclusions,

and implications:

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69

(a) Studies of self-concept and social

support in childhood,

to include a broader age and developmental

range,

conducted in order to examine developmental


studies of self-concept and social

should be

influences;

(b)

support in children with

solid tumors as well as hematogenous malignancies should be


performed;

(c) studies of self-concept and social support in

children with other chronic illnesses should be conducted;


and (d) a control

group of healthy children should be u t i

lized to study self-concept and social support in children


with chronic illnesses such as cancer.
Treatment for childhood cancer has been refined,
prognosis has improved remarkably since the 1970s.

and

Children

are informed openly and honestly about their disease today.


For all these reasons,

early research may not be applicable

to children diagnosed with cancer today.

In the 1970s c hil

dren diagnosed with cancer universally died.


rather than imminent death,

Today survival,

can be anticipated.

examination of the role of social

Further

support as it pertains to

self-concept,

as well as psychosocial

is essential.

Psychological

adjustment to stress,

as well as biological

cure must

be the aim and outcome of interventions.

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72

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76

Operationalization of Johnson's behavioral


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78

Whall, A. L. (1983). The Betty Neuman health care


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Appendix A
Institutional Review Board Approval Forms

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80

THE UNIVERSITY OF
ALABAMA AT BIRMINGHAM
Ortice (it th e Institutional R ev iew Board for H um an U se

FORM 4: IDENTIFICATION AND CERTIFICATION OF


RESEARCH PROJECTS INVOLVING HUMAN SUBJECTS

THE INSTITUTIONAL REVIEW BOARD (IRB) MUST COMPLETE THIS FORM FOR ALL APPLI
CATIONS FOR RESEARCH AND TRAINING GRANTS, PROGRAM PROJECT AND CENTER GRANTS,
DEMONSTRATION GRANTS, FELLOWSHIPS, TRAINEESHIPS, AWARDS, AND OTHER PROPOSALS
WHICH MIGHT INVOLVE THE USE OF HUMAN RESEARCH SUBJECTS INDEPENDENT OF SOURCE
OF FUNDING.
THIS FORM DOES NOT APPLY TO APPLICATIONS FOR GRANTS LIMITED TO THE SUPPORT
OF CONSTRUCTION, ALTERATIONS AND RENOVATIONS, OR RESEARCH RESOURCES.

PRINCIPAL INVESTIGATOR: LISA SOUTH, RN


PROJECT TITLE: THE RELATIONSHIP BETWEEN SELF-CONCEPT AND SOCIAL SUPPORT IN
CHILDREN WITH ACUTE LEUKEMIA AT DIFFERENT STAGES OF CANCER
THERAPY

1.

THIS IS A TRAINING GRANT. EACH RESEARCH PROJECT INVOLVING HUMAN


SUBJECTS PROPOSED BY TRAINEES MUST BE REVIEWED SEPARATELY BY THE
INSTITUTIONAL REVIEW BOARD (IRB).

_X___ 2. THIS APPLICATION INCLUDES RESEARCH INVOLVING HUMAN SUBJECTS. THE


IRB HAS REVIEWED AND APPROVED THIS APPLICATION ON NOVEMBER 13, 1991
IN ACCORDANCE WITH UAB'S ASSURANCE APPROVED BY THE UNITED STATES
PUBLIC HEALTH SERVICE. THE PROJECT WILL BE SUBJECT TO ANNUAL
CONTINUING REVIEW AS PROVIDED IN THAT ASSURANCE.
THIS PROJECT RECEIVED EXPEDITED REVIEW.
_X_

THIS PROJECT RECEIVED FULL BOARD REVIEW.

3.

THIS APPLICATION MAY INCLUDE RESEARCH INVOLVING HUMAN SUBJECTS.


REVIEW IS PENDING BY THE IRB AS PROVIDED BY UAB'SASSURANCE.
COMPLETION OF REVIEW WILL BE CERTIFIED BY ISSUANCE OF ANOTHER
FORM 4 AS SOON AS POSSIBLE.

4.

EXEMPTION IS APPROVED BASED ON EXEMPTION CATEGORY NUMBER(S)_______

fitiHUX CunjwyAvu'Hj-iQ

DATE: NOVEMBER 13, 1991

RUSSELL CUNNINGHAM,,MID.
INTERIM CHAIRMAN OF THE
INSTITUTIONAL REVIEW BOARD
The
i I. j , m : i M ill

nt ALikmi.i .it
!

^ I V. p e j - i r \ R< MiU-v.irJ I A R

R ep ro d u ced with p erm ission o f th e copyright ow ner. Further reproduction prohibited w ithout p erm ission .

81

THE UNIVERSITY OF
ALABAMA AT BIRMINGHAM
O ffice o f the Institutional R eview Board for H u m an b s e

FORM 4: IDENTIF ICATION AND CERTIFICATION OF


RESEARCH PROJECTS INVOLVING HUMAN SUBJECTS

THE INSTITUTIONAL REVIEW BOARD (IRB) MUST COMPLETE THIS FORM FOR ALL APPLI
CATIONS FOR RESEARCH AND TRAINING GRANTS, PROGRAM PROJECT AND CENTER GRANTS,
DEMONSTRATION GRANTS, FELLOWSHIPS, TRAINEESHIPS, AWARDS, AND OTHER PROPOSALS
WHICH MIGHT INVOLVE THE USE OF HUMAN RESEARCH SUBJECTS INDEPENDENT OF SOURCE
OF FUNDING.
THIS FORM DOES NOT APPLY TO APPLICATIONS FOR GRANTS LIMITED TO THE SUPPORT
OF CONSTRUCTION, ALTERATIONS AND RENOVATIONS, OR RESEARCH RESOURCES.

PRINCIPAL INVESTIGATOR: LISA SOUTH, RN


PROJECT TITLE: THE RELATIONSHIP BETWEEN SELF-CONCEPT AND SOCIAL SUPPORT IN
CHILDREN WITH ACUTE LEUKEMIA AT DIFFERENT STAGES OF CANCER
THERAPY

THIS IS A TRAINING GRANT. EACH RESEARCH PROJECT INVOLVING HUMAN


SUBJECTS PROPOSED BY TRAINEES MUST BE REVIEWED SEPARATELY BY THE
INSTITUTIONS REVIEW BOARD (IRB).
X

2.

THIS APPLICATION INCLUDES RESEARCH INVOLVING HUMAN SUBJECTS. THE


IRB HAS REVIEWED AND APPROVED THIS APPLICATION ON NOVEMBER II, 1992
IN ACCORDANCE WITH UAB'S ASSURANCE APPROVED BY THE UNITED STATES
PUBLIC HEALTH SERVICE. THE PROJECT WILL BE SUBJECT TO ANNUAL
CONTINUING REVIEW AS PROVIDED IN THAT ASSURANCE.
THIS PROJECT RECEIVED EXPEDITED REVIEW.
THIS PROJECT RECEIVED FULL BOARD REVIEW.

3.

THIS APPLICATION MAY INCLUDE RESEARCH INVOLVING HUMAN SUBJECTS.


REVIEW IS PENDING BY THE IRB AS PROVIDED BY UAB'S ASSURANCE.
COMPLETION OF REVIEW WILL BE CERTIFIED BY ISSUANCE OF ANOTHER
FORM 4 AS SOON AS POSSIBLE.

4.

EXEMPTION IS APPROVED BASED ON EXEMPTION CATEGORY NUMBER(S)

DATE: NOVEMBER 11, 1992


RUSSELL CUNNINGHAM,M.D.
INTERIM CHAIRMAN OF THE
INSTITUTIONAL REVIEW BOARD

The l.'mver'irv '! Al.iKim.t .it Birmineh.un


MTtinier I.>r.i.m H ill i-I'l ntver-ir. Bmiiev.ira ' AH

R ep ro d u ced with p erm ission o f the copyright ow ner. Further reproduction prohibited w ithout perm ission.

82

I M B S THE UNIVERSITY OF
O H P ALABAMA AT BIRMINGHAM
O ffice o f the Institutional R eview Board for H um an Use

FORM 4: IDENTIFICATION AND CERTIFICATION OF


RESEARCH PROJECTS INVOLVING HUMAN SUBJECTS

THE INSTITUTIONAL REVIEW BOARD (IRB) MUST COMPLETE THIS FORM FOR ALL APPLI
CATIONS FOR RESEARCH AND TRAINING GRANTS, PROGRAM PROJECT AND CENTER GRANTS,
DEMONSTRATION GRANTS, FELLOWSHIPS, TRAINEESHIPS, AWARDS, AND OTHER PROPOSALS
WHICH MIGHT INVOLVE THE USE OF HUMAN RESEARCH SUBJECTS INDEPENDENT OF SOURCE
OF FUNDING.
THIS FORM DOES NOT APPLY TO APPLICATIONS FOR GRANTS LIMITED TO THE SUPPORT
OF CONSTRUCTION, ALTERATIONS AND RENOVATIONS, OR RESEARCH RESOURCES.

PRINCIPAL INVESTIGATOR: LISA SOUTH, RN


PROJECT TITLE: THE RELATIONSHIP BETWEEN SELF-CONCEPT AND SOCIAL SUPPORT IN
CHILDREN WITH ACUTE LEUKEMIA AT DIFFERENT STAGES OF CANCER
THERAPY

I.

THIS IS A TRAINING GRANT. EACH RESEARCH PROJECT INVOLVING HUMAN


SUBJECTS PROPOSED BY TRAINEES MUST BE REVIEWED SEPARATELY BY THE
INSTITUTIONAL REVIEW BOARD (IRB).

X___2. THIS APPLICATION INCLUDES RESEARCH INVOLVING HUMAN SUBJECTS. THE


IRB HAS REVIEWED AND APPROVED THIS APPLICATION ON DECEMBER 08, 1993
IN ACCORDANCE WITH UAB'S ASSURANCE APPROVED BY THE UNITED STATES
PUBLIC HEALTH SERVICE. THE PROJECT WILL BE SUBJECT TO ANNUAL
CONTINUING REVIEW AS PROVIDED IN THAT ASSURANCE.
THIS PROJECT RECEIVED EXPEDITED REVIEW.
_X_

THIS PROJECT RECEIVED FULL BOARD REVIEW.

3.

THIS APPLICATION MAY INCLUDE RESEARCH INVOLVING HUMAN SUBJECTS.


REVIEW IS PENDING BY THE IRB AS PROVIDED BY UAB'SASSURANCE.
COMPLETION OF REVIEW WILL BE CERTIFIED BY ISSUANCE OF ANOTHER
FORM 4 AS SOON AS POSSIBLE.

4.

EXEMPTION IS APPROVED BASED ON EXEMPTION CATEGORY NUMBER(S)_______

DATE: DECEMBER 08, 1993


i 1

Russell cunningham
cunningh
, m .d
INTERIM CHAIRMAN OF THE
INSTITUTIONAL REVIEW BOARD

T h e U n iv ersity o f A labam a at Birm ingham


212 M ortim er Jordan H all 1825 U niversity Boulevard
B irm ingham , A labam a 35294-2010 (205) 934-3789 FAX (205) 975-5977

R ep ro d u ced with p erm ission o f the copyright ow ner. Further reproduction prohibited w ithout p erm ission.

Appendix B
Program Director Approval Form

R ep ro d u ced with p erm ission o f th e copyright ow ner. Further reproduction prohibited w ithout perm ission.

84

I grant permission for Lisa South to seek the p a r t i c i


pation of children with leukemia in her research study, and
to administer the Pier's Harris Children's Self-Concept
Scale and the PRQ 85, Part 2 to these participants.

(Circle o n e ) :
YES

Date

NO

Signature

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Appendix C
Guidelines for Administration of Re search Tools

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86

G uidelines for Administering the


Self-Concept Tool an d the Social Support Tool
1. Offer the parent or guardian a copy of the questionaires and the information and demographic form. Explain that
the questionaires "Consists of simple questions about how
the child feels about themselves.
right or wrong answers.

Explain that there are no

If the child answers the way they

really feel, then the answer is right."


2. Allow the parent or guardian time to read the infor
mation letter and to complete and sign the
demographic/consent form.

Ask if they have any questions

and answer these. Ask the child if they agree to participate


and complete the questionaires.

If the child agrees, and

parent or guardian has signed consent, proceed with the


questionaires.
3. To develop rapport with the child, state "The p u r
pose of this scale is to find out how you really feel about
yourself.

If you answer the way you really feel, then it's

the right answer.

Sometimes

your parents or teachers might

be asked to say how they think you f e e l , but this is your


chance to say how you feel".
4. To assure that the child answers the questions on
the PHCSCS scale honestly,

instruct them to "answer each

item on the scale the way you really feel and not the way
you think you ought to feel".
5. To assure that the child does not become anxious
about completing the scale,
like a game.

state,

"This is not a test, more

So there are no right or wrong answers.

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87

6. Give a booklet and pencil

to the child and ask the

child to turn to the first page and complete the identifying


information.

Then state,

"I would like you to read the

directions silently as I read them aloud.


7. Emphasize that every item should be circled YES or
NO. All items should be answered even if they have a hard
time deciding which answer to mark.
8. Since some children may have difficulty reading and
understanding the items,

read each item aloud as the child

reads it silently. Read each item twice.

I give the child

the option of reading the questions and answering them


silently or having me read the items for them as they a n
swer.

Younger children may require/request the items be

read.
9. Check to make sure the child is completing the scale
correctly. Ask if there are any questions.
10. Any word that the child does not understand,

or is

uncertain about, may be briefly defined.


11.

If some children are reluctant to give a simple YES

or NO answer,

tell them that they should answer the item the

way they u sually f e e l .


12.

Items 32 and 72 should not be omitted even if the

child is an only child.

Those children who do not have a

sibling should be told to answer No to item 32 and YES to


i t em 72.

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88

13. Allow the child to proceed at his or her own pace.


14. After the PHCSCS is completed,

collect the booklet

and hand out the PRQ-85 Part 2.


15. State "These are some questions to find out more
about you. You will mark these statements differently.
are 7 possible answers.

There

Look at the scale at the top of the

page (Point out the scale).

#1 means that you really don't

agree with the sentence at all. #2 means that you Mostly


don't agree with the sentence.

#3 means that you disagree a

little bit. #4 means that you don't have any feeling about
the sentence on way or another.

#5 means that you agree a

little bit. #6 means that you mostly agree with the s e n


tence.

#7 means that you really agree with the sentence.

16. Be sure that the child understands the scale before


beginning.
17. Offer to read each statement aloud as the child
reads them silently.
18. Ask the child completes the questionnaire,
there are any questions.

ask if

Offer to explain the scale again if

needed at any time while the questionnaire is being c o m ple t


ed.
19. Allow the child to work at his own pace.
20. Collect the questionnaire when the child has f in
ished. Offer thanks for participation.

Remind them that they

may call the number on the information letter if they have


any questions.

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Appendix D
Cover Letter

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90

Dear Parent,
I am a graduate student in nursing at the University of
Alabama School of Nursing, University of Alabama at
Birmingham.
My major is maternal-child nursing.
In order to complete dissertation research requirements for
my doctoral degree, I am conducting a study of self-concept
and social support of school age children with leukemia.
Because you have a child fitting this description, I am
asking that you give permission for your child to partici
pate in the study.
Participation in the study involves completion of the dem o
graphic questionnaire attached, by the parent of the child.
After the questionnaire has been returned, your child will
be asked to complete the Piers-Harris Children's Self C o n
cept Scale and the PRQ 85, Part 2 Social Support Scale.
It
will take approximately 30 minutes for your child to com
plete the tools.
All information obtained for this study will be treated
confidentially and individual names will remain anonymous.
The questionnaires are assigned numbers, so that no names
will be used,
all information will be recorded as group
data, so that no individual can be identified.
No risks to
participants has been identified.
Results of the study will
be made available to you upon request.
Participation in the study is voluntary and you may withdraw
your child from the study until the point at which the data
have been collected.
If you agree for your child to p ar tic
ipate in the study, I would appreciate you completing,
signing, and returning the attached questionnaire.
Your
willingness to participate will be greatly appreciated.
Should you have any questions regarding the study, please
feel free to contact me at (205) 822-6507.

Sincerely,

Lisa South, R . N . , D.S.N.

candidate

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Appendix E
Demographic Questionnaire/Consent

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92
Demographic Questionnaire
ChiId's Name:
Child's date of birth:
Child's sex (circle one):

MA LE

FEMALE

C h i l d s race

BLACK

WH ITE

(circle one):

Child's grade in school

(circle one):

OTHER:
3

Chi Id's d i a a n o s i s :
Date of d i a a n o s i s :
Stage of therapy:______
Present disease status:
Does your child have any chronic illness other than le uke
mia, or obvious physical or mental limitations?
(circle
one):
YES

NO

If yes, please specify illness or limitation:

_____________

The completion of this questionnaire and my signature below,


signify that consent is granted for my child to participate
in the study to be conducted by Ms. Lisa South.
I under
stand that I am not waiving any of my legal rights by s i g n
ing this form.
M y signature below indicates that I have
received a copy of the informed consent letter.

Date

Signature of Parent or Guardian

Date

Signature of Witness

As a school age child, I agree to participate in the re


search conducted by Ms. Lisa South.
I understand that my
participation involves answering simple questions about
myself.

Date

Signature of Parent,

Guardian,

or Child

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G R A D U A T E SCH OOL
U N IV E R S IT Y O F A L A B A M A A T B IR M IN G H A M
D IS S E R T A T IO N A P P R O V A L F O R M

N a m e o f C a n d id a te

L is a p.

s out h__________________________________

M ajor S u b j e c t _______ M a t e r n a l C h ild H e a l t h N u r s i n g _______________


T itle o f D isserta tio n

The R e l a t i o n s h ip B e t w een S e l f C o n c e p t and

_________ S o ci al S u p p o r t

in S c h o o l A g e C h i l d ren w i t h L e u k e m i a

D isserta tio n C om m ittee:

/ ( . I - .

ILll

Z'-

C hairm an

A.
f'

D irecto r o f G raduate Program


D ea n , U A B G raduate S ch ool

D a te

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