utritional intervention study focusing on maintaining and improving ADL of the older inpatient
Not Applicable
Recruiting
- Conditions
- sarcopenia, frailty, fracture, cerebral infarction
- Registration Number
- JPRN-UMIN000051159
- Lead Sponsor
- Kansai Electric Power Medical Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Subjects with serious heart disease, renal disease, or liver disease (2) Those who are using steroids (3) Individuals who have difficulty observing and evaluating dietary guidance due to dementia, mental illness, etc. (4) Those who have implanted cardiac pacemakers or implanted cardioverter-defibrillators (5) Individuals who are deemed inappropriate for this clinical study by the research implementation supervisor or research co-investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in muscle mass, strength and physical function over 2 months
- Secondary Outcome Measures
Name Time Method Changes in stratum corneum water content, changes in skin elasticity, and changes in blood test results (hemoglobin, aspartate aminotransferase, alanine aminotransferase, creatinine, blood urea nitrogen, estimate glomerular filtration rate, serum albumin, C-reactive protein, rapid turnover protein) over the 2 months