Comparison of the effect of a Proprioceptive Neuromuscular Facilitation (PNF)-based virtual reality intervention versus real PNF exercises in stroke
Not Applicable
Recruiting
- Conditions
- Chronic Stroke Survivors.Stroke, not specified as haemorrhage or infarction
- Registration Number
- IRCT20240406061422N1
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 28
Inclusion Criteria
First stroke experience
A minimum of 6 months to a maximum of 4 years since stroke
Ability to sit independently on a chair during the intervention
Ability to understand and follow instructions
Brunnstrom stage 3 or higher for upper extremity
Exclusion Criteria
Severe visual impairment that makes it difficult to interact with virtual reality tool
History of previous mood disorders or use of related medications
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pper Extremity motor performance. Timepoint: Pre ,Post, After 1 month follow up. Method of measurement: Fugl-Meyer Assessment, Motor Activity Log.;Cognitive performance. Timepoint: Pre ,Post, After 1 month follow up. Method of measurement: Montreal Cognitive Assessment, Wisconsin Card Sorting Test ,Forward and backward Digit Span Test.;Occupational performance. Timepoint: Pre ,Post, After 1 month follow up. Method of measurement: Canadian Occupational Performance Measure.
- Secondary Outcome Measures
Name Time Method Depression and Anxiety. Timepoint: Pre, Post, After 1 month follow up. Method of measurement: Hospital Anxiety and Depression Scale.