Purpose
PSFS is a self-report measure that assess a patient's perception of spasticity frequency and severity following a spinal cord injury.
Acronym
PSFS
Area of Assessment
Bodily Functions
Assessment Type
Patient Reported Outcomes
Administration Mode
Paper & Pencil
Cost
Free
- Composed of 2 parts:
1) A self-report measure with items on 5-point scales developed to augment clinical ratings of spasticity and provides a more comprehensive assessment of spasticity.
2) A 3-point scale assessing the severity of spasms.
- Spasm Frequency:
0 = No spasm
1 = Mild spasms induced by stimulation
2 = Infrequent full spasms occurring less than once per hour
3 = Spasms occurring more than once per hour
4 = Spasms occurring more than 10 times per hour
- Spasm Severity:
1 = Mild
2 = Moderate
3 = Severe
- If the patient indicates no spasms in Part 1, then they do not proceed to Part 2.
Required Training
Reading an Article/Manual
Instrument Reviewers
Initially reviewed by the Rehabilitation Measures Team in 2011; Updated by the TBI EDGE task force and Christopher Newman, PT, MPT, NCS, Jennifer Kahn, PT, DPT, NCS and the SCI EDGE task force of the Neurology Section of the APTA in 2012.
ICF Domain
Body Structure
Body Function
Measurement Domain
Motor
Professional Association Recommendation
Recommendations for use of the instrument from the 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 (Vestibular EDGE) are listed below. These recommendations were developed by a panel of research and clinical experts using a modified Delphi process.
For detailed information about how recommendations were made, please visit: ANPT Outcome Measures Recommendations (EDGE)
Abbreviations:
HR
Highly Recommend
R
Recommend
LS / UR
Reasonable to use, but limited study in target group / Unable to Recommend
NR
Not Recommended
Recommendations for use based on acuity level of the patient:
Acute
(CVA < 2 months post)
(SCI < 3 month post)
(Vestibular < 6 weeks post)
Subacute
(CVA 2 to 6 months)
(SCI 3 to 6 months)
Chronic
(> 6 months)
SCI EDGE
LS
LS
LS
Recommendations based on SCI AIS Classification:
AIS A/B
AIS C/D
SCI EDGE
LS
LS
Recommendations for entry-level physical therapy education and use in research:
Students should learn to administer this tool? (Y/N)
Students should be exposed to tool? (Y/N)
Appropriate for use in intervention research studies? (Y/N)
Is additional research warranted for this tool (Y/N)
SCI EDGE
No
Yes
Yes
Not reported
Considerations
- May not adequately record flexor and extensor spasms (Hsieh et al, 2008)
- The current form of the PSFS was modified from its original version to include spasm frequency and severity. (Priebe et al, 1996)
Do you see an error or have a suggestion for this instrument summary? Please e-mail us!