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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05809219
Other study ID # NSTC 112-2320-B-039-008
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date July 10, 2023
Est. completion date February 29, 2024

Study information

Verified date September 2023
Source China Medical University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
1 hour combined intervention ( Exercise and nutrition)
Subjects take oral supplement after exercise in the time period between 1-2 hours. They will take oral supplement during hemodialysis treatment.
3 hours combined intervention ( Exercise and nutrition)
All procedures between "1 hour combined intervention" and "3 hours combined intervention" are the same. The only one different is the time interval between exercise and nutrition. In this arm, the time interval of exercise and nutrition is 2.5 to 4 hours. When we recruiting subjects, all interventions will be clearly introduced to them, including the same and the different parts among them.
Dietary Supplement:
Nutrition intervention
Subjects only take oral supplement during hemodialysis treatment. The oral supplement is the same as the "1 hour combined intervention" and "3 hours combined intervention".

Locations

Country Name City State
Taiwan China Medical University Hospital Taichung City

Sponsors (1)

Lead Sponsor Collaborator
China Medical University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

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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