The feasibility and safety study of the central nervous functional recovery therapy using a wearable human support robot HAL for the patients with the central motor dysfunction.
Not Applicable
Recruiting
- Conditions
- The central moter dysfunction associated with stroke, cerebrospinal injury, cerebrospinal tumor and neuromusclar disease
- Registration Number
- JPRN-UMIN000014336
- Lead Sponsor
- niversity of Tsukuba
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 15
Inclusion Criteria
Not provided
Exclusion Criteria
1. It is difficult to perform the volantary movement of the limbs in accordance with the instructions due to the disturbance of consciousness or dementia. 2. It is difficult to wear HAL or train using HAL due to the severe deformation of the skeletal system. 3. Patients has a complication, which can disturb the treatment using HAL. 4. The biological edectrode for HAL can not be affixed to patient's skin due to the skin disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Adverse event 2. Failure of HAL and ancillary equipment 3. Feasibility of study protocol
- Secondary Outcome Measures
Name Time Method