Verification of muscle strengthening effect of Neuromuscular electrical stimulation using wearable small electric stimulation device in patients with stable COPD: randomized controlled trials
Not Applicable
Recruiting
- Conditions
- Chronic obstructive pulmonary disease
- Registration Number
- JPRN-UMIN000034790
- Lead Sponsor
- Matsusaka Municipal Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with central and peripheral neuropathy, progressive cancer, using cardiac pacemakers, contraindicated for cardiopulmonary exercise test
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint is fat free mass index, and it is investigated before intervention 8 week and 6 months.
- Secondary Outcome Measures
Name Time Method The secondary endpoint is fat free mass index, right upper limb muscle mass, left upper limb muscle mass, right lower limb muscle mass, left lower limb muscle mass, total muscle mass,% VC,% FEV1,FEV 1%,% FVC, step, METs, MVPA,6 minutes walking distance,WBI, grip, walking speed (m / sec), right upper limb circumference, left upper limb circumference, right circumference of right leg, left lower limb circumference, body weight,BMI, NRADL, CAT, m-MRC are investigated before intervention 8 weeks and 6 months.