Testing if a device that provides arm weight support is usable by stroke survivors.
Not Applicable
- Conditions
- Health Condition 1: G00-G99- Diseases of the nervous system
- Registration Number
- CTRI/2024/05/067363
- Lead Sponsor
- Christian Medical College Vellore
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Stroke survivor prescribed for upper limb therapy.
MoCA greater than 26/30
Minimum 10 cm voluntary movement with weight support from MARS
Exclusion Criteria
Shoulder subluxation greater than 0 by fingerbreadth palpation method
Pain in shoulder/elbow joints, visual analogue scale – VIS greater than 3/10
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method System Usability ScaleTimepoint: After a day or within a week from enrolment.
- Secondary Outcome Measures
Name Time Method Box and Block TestTimepoint: Baseline;Fugl Meyer AssessmentTimepoint: Baseline;Grip strength with 0%, 50% and 100% weight supportTimepoint: Baseline;Intrinsic Motivation Inventory (IMI)Timepoint: After two therapy sessions;Work Area with 0%, 50% and 100% weight supportTimepoint: Baseline