Health Condition 1: F- Physical Rehabilitation and Diagnostic Audiology
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Unilateral upper limb impairment caused by a single stroke at least 2 weeks to 6 months prior to the start of the study. 2. Healthy (or corrected-to-normal) vision and hearing abilities to understand the information communicated by the research investigators. 3. Ambulatory, and/or able to travel to research study location. 4. CMSA: Level 3 or greater for hand function, and Shoulder pain 5. MMSE score = 24 6. Capacity to consent is established
Exclusion criteria
Exclusion criteria: 1. Diagnosis of a neurological disorder other than stroke that can impede in hand function therapy (e.g. peripheral neuropathy, myopathies, Parkinson’s disease etc.) 2. Participants suffering from osteoarthritis or other musculoskeletal or neuromuscular disorders that affect hand function. 3. Participants with severe systemic disease that has an impact on hand function 4. Participants with severe spasticity or contractures, that has a limiting impact on hand function therapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Efficacy of the IRegained MyHandTM System and assessment of objective & subjective changes as a result of the hand function trainingTimepoint: 16 to 18 sessions of training | — |
Secondary
| Measure | Time frame |
|---|---|
| To observe objective and subjective changes in hand function as a result of hand-function trainingTimepoint: 16 to 18 sessions of training | — |
Countries
India
Contacts
ApoKOS Rehabilitation Center