Clinical trial
Exercise and Taurine Supplementation on Intramuscular Fat in Older Women With Obesity
Active, not recruiting · Not applicable · 1 countries · Registry ID NCT07730255
What this study is about
This randomized clinical trial aims to investigate the effects of multicomponent concurrent exercise training associated or not with taurine supplementation on intramuscular fat infiltration, physical performance, transcriptomic profile, and metabolomic profile in older women with obesity. Forty women aged 60 to 75 years with obesity will be randomized into four groups: control, exercise, taurine, and exercise plus taurine. The intervention will last 16 weeks. Outcomes include magnetic resonance imaging, body composition, muscle biopsy, blood biomarkers, functional capacity tests, transcriptomic analysis, and metabolomic analysis.
Basic eligibility
Full registry criteria
Treatments and study arms
Concurrent Exercise Training
Participants will perform supervised concurrent exercise training three times per week for 16 weeks. Exercise sessions will include warm-up, resistance exercises, aerobic training, and stretching exercises, according to American College of Sports Medicine (ACSM) recommendations for older adults.
Taurine
Participants will receive 3 grams per day taurine supplementation administered orally in capsules for 16 weeks.
Placebo
Participants will receive placebo capsules identical in appearance to taurine capsules.
Primary outcomes
Intramuscular fat fraction assessed by magnetic resonance imaging (MRI) using the Dixon technique, reported as percentage (%) of fat within the muscle tissue. Change is calculated from baseline to Week 16.
Skeletal muscle biopsy samples will be analyzed using RNA sequencing to characterize changes in the skeletal muscle transcriptomic profile following the intervention.
Plasma samples will be analyzed using untargeted metabolomic analysis to evaluate changes in the plasma metabolomic profile after 16 weeks of intervention.
Plasma taurine concentration will be measured before and after the 16-week intervention.
Study locations
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