Invloed van robotische handschoen op functioneren van de arm- en handfunctie van patiënten die een beroerte door hebben gemaakt
- Conditions
- English: stroke, CVA, arm function, hand functionNederlands: beroerte, armfunctie, handfunctie
- Registration Number
- NL-OMON25281
- Lead Sponsor
- Roessingh Research and Development (Enschede, the Netherlands)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 10
Inclusion Criteria
• Patients should be clinically diagnosed with unilateral ischemic or hemorrhagic stroke
• Between 18-80 years of age
Exclusion Criteria
• People with severe sensory problems of the affected hand.
• People with severe acute pain of the affected hand.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The main study parameters are outcomes related to functional hand performance in ADL.
- Secondary Outcome Measures
Name Time Method Secundary study parameters are related to user acceptance, perceived use, amount of use, changes in hand motor function and impact on quality of life.