Beruflich Dokumente
Kultur Dokumente
Measu
res:
FIM®
instru
ment
(FIM);
FIM®
is a
trade
mark
of the
Unifor
m
Data
Syste
m for
Medic
al
Rehab
ilitatio
n, a
divisio
n of
UB
Found
ation
Activit
ies,
Inc.
Link to instrument
Uniform Data System for Medical Rehabilitation (external
link)
Title of Assessment
FIM® instrument (FIM); FIM® is a trademark of the
Uniform Data System for Medical Rehabilitation, a division
of UB Foundation Activities, Inc.
Acronym
Instrument
Initially reviewed by the Rehabilitation Measures Team;
Reviewer(s)
Updated by Eileen Tseng, PT, DPT, NCS, Rachel
Tappan, PT, NCS, and the SCI EDGE task force of the
Neurology Section of the APTA in 2012; Updated by
Tammie Keller, PT, DPT, MS and the TBI EDGE task
force of the Neurology Section of the APTA; Updated by
Dev Kegelmeyer, PT, DPT, MS, GCS and the PD EDGE
task force of the neurology section of the APTA in 2013.
Summary Date
10/6/2015
Purpose
Provides a uniform system of measurement for disability
based on the International Classification of
Impairment, Disabilities and Handicaps; measures the
level of a patient's disability and indicates how much
assistance is required for the individual to carry out
activities of daily living.
Description
Contains 18 items composed of:
o 13 motor tasks
o 5 cognitive tasks (considered basic
activities of daily living)
Tasks are rated on a 7 point ordinal scale that
ranges from total assistance (or complete
dependence) to complete independence
Scores range from 18 (lowest) to 126 (highest)
indicating level of function
Scores are generally rated at admission and
discharge
Dimensions assessed include:
o Eating
o Grooming
o Bathing
o Upper body dressing
o Lower body dressing
o Toileting
o Bladder management
o Bowel management
o Bed to chair transfer
o Toilet transfer
o Shower transfer
o Locomotion (ambulatory or wheelchair
level)
o Stairs
o Cognitive comprehension
o Expression
o Social interaction
o Problem solving
o Memory
Area of Assessment
Activities of Daily Living
Body Part
Not Applicable
ICF Domain
Activity
Domain
ADL; Cognition; Motor
Assessment Type
Observer
Length of Test
31 to 60 Minutes
Time to Administer
30-45 minutes
Number of Items
18
Equipment Required
May vary based on level and impairment category
measured.
Training Required
Yes, certification in administering the FIM instrument is
required prior to use. Training is available through
UDSMR at: www.udsmr.org.
Type of training
Reading an Article/Manual
required
Cost
Not Free
Actual Cost
A license to use the FIM instrument may be obtained
at: http://www.udsmr.org.
Age Range
Adult: 18-64 years; Elderly adult: 65+
Administration Mode
Paper/Pencil
Diagnosis
Geriatrics; Multiple Sclerosis; Pain; Spinal Cord Injury;
Stroke
Populations Tested
Brain Injury
Geriatrics
Multiple Sclerosis
Orthopedic Conditions including Low Back Pain
Parkinson's Disease
Spinal Cord Injury
Stroke
Standard Error of
Not Established
Measurement (SEM)
Minimal Detectable
Not Established
Change (MDC)
Minimally Clinically
Stroke:
Important Difference
(MCID)
(Beninato et al, 2006; n = 113; mean age = 63.9 (14.3)
years; mean FIM score at admission = 63.4 (24.4) points,
Acute Stroke)
Cut-Off Scores
Not Established
Normative Data
SCI:
Stroke:
Parkinson's Disease:
Rehabilitation Patients:
Rehabilitative patients:
SCI:
Face Validity
SCI:
(Grey and Kennedy, 1993; Chronic SCI)
Stroke:
Motor subscale:
o Large effect size with standardized
response mean = 1.3
Professional
Recommendations for use of the instrument from the
Association
Recommendations Neurology Section of the American Physical Therapy
Association’s Multiple Sclerosis Taskforce (MSEDGE),
Parkinson’s Taskforce (PD EDGE), Spinal Cord Injury
Taskforce (PD EDGE), Stroke Taskforce (StrokEDGE),
Traumatic Brain Injury Taskforce (TBI EDGE), and
Vestibular Taskforce (VEDGE) are listed below. These
recommendations were developed by a panel of research
and clinical experts using a modified Delphi process.
Abbreviations:
HR Highly Recommend
R Recommend
LS / Reasonable to use, but limited study in
UR target group / Unable to Recommend
NR Not Recommended
Recommendations for use based on acuity level of the
patient:
Acute Subacute Chronic
(CVA < 2 (CVA 2 to (> 6
months 6 months) months)
post) (SCI 3 to 6
(SCI < 1 months)
month post)
(Vestibular
< 6 weeks
post)
SCI EDGE R R R
StrokEDGE HR UR UR
Instrument in PDF
Yes
Format
Approval Status
Approved