MedPath

Interactive training devices for people with hand weakness

Phase 1
Recruiting
Conditions
Health Condition 1: null- Stroke
Registration Number
CTRI/2017/06/008860
Lead Sponsor
Department of Bioengineering Christian Medical College Vellore
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

Stroke patients with Brunstrom stage 3 and above hemiparesis

Exclusion Criteria

Movement restricted due to musculo-skeletal problems, patients with global aphasia, patients with cognitive deficit and other neurological disorders.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. The primary outcome would be the count of movements performed, movement range and quality of movement. The therapist assisted rehabilitation session will be compared with the new sensor based rehabilitation. <br/ ><br>2. FMA (Fugl-Meyer Assessment of motor recovery after stroke) <br/ ><br>3. System Usability Scale (SUS)Timepoint: Study 1 :- <br/ ><br>Four phases of assessment, <br/ ><br>Day 1, Day 3, Day 14 and Day 28 <br/ ><br>SUS will be given only on the last day (28th). <br/ ><br> <br/ ><br>Study 2 :- <br/ ><br>One time assessment - Day 1
Secondary Outcome Measures
NameTimeMethod
1. Clinical assistance providedTimepoint: Qualitative measure recorded on a daily basis in study 1 (from day 1 to day 28). <br/ ><br> <br/ ><br>One time measurement - day 1 in study 2
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