Comparison of Effects of upper limb rehabilitation robotics application method in Spinal Cord Injury Patients
Not Applicable
Completed
- Conditions
- Diseases of the nervous system
- Registration Number
- KCT0006389
- Lead Sponsor
- ational Rehabilitation Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
1) age 19 years old or above
2) time since injury was of less than 2 year
3) AIS C, D
4) able to understand instructions of the protocol
5) Patients who decide to participate in the study directly with their own or their parents' consent
Exclusion Criteria
1) Patients with obvious diseases that may cause muscle weakness other than spinal cord injury (e.g. neuromuscular disease)
2) Patients with severe upper limb stiffness above MAS 3
3) Patients who are restricted in wheelchairs or chairs for more than 30 minutes
4) patients with severe shoulder pain
5) Patients whose upper extremity ROM movement is limited by more than 50%
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Arm trajectory measurement using trakSTAR
- Secondary Outcome Measures
Name Time Method Manual muscle test;Modified ashworth scale;Korean version of spinal cord independence measure-3;The capabilities of upper extremity instrument (CUE);Visual analoge scale