Safety and feasibility study of mobility support using excretion support robot
- Conditions
- Patients with spinal cord injury, stroke, bone joint diseases, life inactive disease (disuse syndrome), and postoperative such as spinal disease and so on.
- Registration Number
- JPRN-UMIN000035219
- Lead Sponsor
- niversity of Tsukuba
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 10
Not provided
Patients who conflict with one of the following criteria are excluded and not subject to this clinical study. 1. A patient who is judged to have the following findings by the research director or the research assignee. 1) A patient who have marked muscle weakness and motor paralysis on both side upper limbs (Manual Muscle Testing: MMT 0 to 1) 2) A patient with advanced immobility, contraction and ataxia. 3) A patient who have difficulty in rehabilitation in the training room. 4) A patient who is judged to be difficult to understand instructions (including patients who can not understand instructions and express their own condition due to aphasia). 5) A patient who have severe spasticity, deformation, contracture of the lower limbs, judged to be difficult to stand up and transfer. 2. A patient who is judged inappropriate to participate in the study by the research director or research assignee.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Safety (status of occurrence of adverse event, situation of malfunction of this equipment) Feasibility (completion rate of movement using this equipment)
- Secondary Outcome Measures
Name Time Method