Sarcopenia Clinical Trial
Official title:
The Effect of Different Post-exercise Oral Nutritional Supplement Intake Timing on Sarcopenia Indicators in Hemodialysis Patients
Verified date | September 2023 |
Source | China Medical University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Objective: To assess the effect of different post-exercise oral nutritional supplement intake timing on sarcopenia indicators in hemodialysis patients. Study Design: 24-weeks Randomized Control Trial (RCT), includes 12-wk intervention period and 12-week follow up period. Setting & Participants: Maintenance hemodialysis patients who were older than 20 years old meet sarcopenia diagnosis criteria. Intervention: Group A: During intervention period, participants have 3 times exercise program per week. Each program is 30 minutes of resistance exercise and aerobic exercise. Participants take oral supplement in 1 to 2 hours after exercise program. Group B: Participants have the same exercise program and oral supplement as Group A. However, they take oral supplement in 2.5-4 hours after exercise program. Group C: Participants only take oral supplement. Control group: Participants maintain usual diet and physical activity without any intervention.
Status | Enrolling by invitation |
Enrollment | 200 |
Est. completion date | February 29, 2024 |
Est. primary completion date | February 29, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years and older |
Eligibility | Inclusion Criteria: - Hemodialysis treatment longer than 3 months - Hemodialysis treatment 3 times treatment per weeks - Kt/V=1.2 or URR=65% - Taking foods by oral - Meeting the criteria of sarcopenia. Exclusion Criteria: - Soy allergy - Amputation - Significantly edema - Receiving palliative care - Severe angina - Unstable arrhythmias - Severe infection - Heart failure (class 4 of New York Heart Association scale) - Central venous catheter or femoral arteriovenous fistula - Pacemaker - Pregnancy - Severe paleness - Severe difficulty breathing - Chest pain - Hospitalization 3 months before recruited in this study - Oral supplement intolerance diagnosed by the doctor or dietitian - Bone injury/nerve damage/cognition impairment affecting physical activity intervention |
Country | Name | City | State |
---|---|---|---|
Taiwan | China Medical University Hospital | Taichung City |
Lead Sponsor | Collaborator |
---|---|
China Medical University Hospital |
Taiwan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Appendicular skeletal muscle mass | The weight of appendicular skeletal muscle mass. This is one of the sarcopenia indicator. | Change from baseline appendicular skeletal muscle mass at 3 months | |
Primary | Appendicular skeletal muscle mass | The weight of appendicular skeletal muscle mass. This is one of the sarcopenia indicator. | Change from baseline appendicular skeletal muscle mass at 6 months | |
Primary | Muscle strength | The measurement of handgrip strength. This is one of the sarcopenia indicator. | Change from baseline muscle strength at 3 months | |
Primary | Muscle strength | The measurement of handgrip strength. This is one of the sarcopenia indicator. | Change from baseline muscle strength at 6 months | |
Primary | Physical performance | Measuring whether the of 6-meter walk is less than 1.0 m/s or not. This is one of the sarcopenia indicator. | Change from baseline physical performance at 3 months | |
Primary | Physical performance | Measuring whether the of 6-metre walk is less than 1.0 m/s or not. This is one of the sarcopenia indicator. | Change from baseline physical performance at 6 months |
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