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utritional intervention for hemodialysis patients with locomotive syndrome

Not Applicable
Conditions
locomotive syndrome hemodialysis
Registration Number
JPRN-UMIN000032457
Lead Sponsor
Shinkohkai Murakamikinen Hospital Department of Nutrition
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

Absolute contraindication Acute myocardial infarction within 2 days Unstable angina Arrhymia Arotic stenosis Symptomatic heart failure Acute myocarditis or acute pericarditis Acute pulmonary embolism or acute pulmonary infarct Arotic dissection Difficult communication due to mental illness Relative contraindication Stenosis of the left coronary artery main pipe section Moderate stenosis of valve Electrolyte abnormalities Severe hypertension Tachyarrthymia or bradyarrthythmia Hypertrophic cardiomyopathy or other Inability to exercise test due to mental illness or physical disability Seriously atrioventricular block

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Physical component summary of SF-36
Secondary Outcome Measures
NameTimeMethod
Mental component summary and Role/Social component summary of SF-36, Prevalence of locootive syndrome, Skeletal muscle mass indexs,Nutritional status
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