Clinical application of neuromuscular electrical stimulation therapy for Locomotive syndrome.
Not Applicable
- Conditions
- ocomotive syndrom
- Registration Number
- JPRN-UMIN000026253
- Lead Sponsor
- Hiroshima University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 29
Inclusion Criteria
Not provided
Exclusion Criteria
1: diabetes mellitus 2: neuromuscular disorders 3: hypersensitivity of alcohol
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measurement of lower muscle strength is examine using the BIODEX system. Measurement is baseline, after 4 weeks, and 8 weeks.
- Secondary Outcome Measures
Name Time Method Secondary outcomes are muscle thickness, balance performance, and motor unit recruitment. Measurement of muscle thickness is examine using the ultrasound. Measurement of balance performance is examine using the Berg balance scale. Measurement of motor unit recruitment is examine using the multi-channel surface electromyography. Measurement is baseline, after 4 weeks, and 8 weeks.