Combined effects of botulinum toxin and splinting therapy on upper limb spasticity
Not Applicable
Recruiting
- Conditions
- patients with upper limb spasticity
- Registration Number
- JPRN-UMIN000032170
- Lead Sponsor
- Hamamatsu City Rehabilitation Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1)patients with no adaptation to botulinum toxin A 2)Patients with disturbance of consciousness or higher brain dysfunction who were considered to be inappropriate to participate in the study 3)Patients with severe limitation of range of motion because of joint contracture
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method passive range of motion
- Secondary Outcome Measures
Name Time Method Modified Ashworth Scale Brunnstrom recorvery stage Disability assessment scale attachment time of splint status of implementation of self training