Post-stroke arm/hand training at home.
- Conditions
- Stroke, CVA, beroerte
- Registration Number
- NL-OMON29571
- Lead Sponsor
- Roessingh Research and Development b.v.
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
1. Patients with an unilateral ischemic or hemorrhagic stroke, between 6 and 12 months post-stroke;
2. Between 18 and 80 years of age;
Exclusion Criteria
1. Patients who receive additional therapy of the affected arm/wrist/hand during participation of the study;
2. Patients who are not eligible to join normal rehabilitation (psychological issues, patients with near complete paralysis etc.);
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main study parameters are outcomes related to user acceptance, including usability, satisfaction, motivation and compliance (Intrinsic Motivation Inventory, System Usability Scale, Qualitative interview about experience of use).
- Secondary Outcome Measures
Name Time Method Measures to examine general motor function, perceived use and participation (The Action Research Arm Test (ARAT), the upper extremity part of the Fugl-Meyer (FM) test, the Box & Blocks test (BBT), Motor Activity Log (MAL), the Stroke Impact Scale (SIS), kinematics and EMG).