Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT07730255

Exercise and Taurine Supplementation on Intramuscular Fat in Older Women With Obesity

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Notify Me

Key information

Age range

60 year–75 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Escola de Educação Física e Esporte de Ribeirão Preto, Ribeirão Preto, São Paulo.

Ribeirão Preto, São Paulo, 14040-900, Brazil

About this study

Aging and obesity are associated with important physiological, metabolic, and functional alterations, including increased intramuscular fat infiltration, also known as myosteatosis. Intramuscular fat infiltration is associated with reduced muscle quality, impaired physical performance, metabolic dysfunction, insulin resistance, and increased risk of morbidity and mortality in older adults.

Physical exercise is recognized as an important non-pharmacological strategy to improve muscle function and metabolic health. In addition, taurine supplementation has demonstrated anti-inflammatory and metabolic effects that may contribute to the reduction of intramuscular fat accumulation and improvement of skeletal muscle health.

However, the synergistic effects of concurrent exercise training associated with taurine supplementation on intramuscular fat infiltration and molecular mechanisms involved in older women with obesity are still unclear.

Therefore, this randomized clinical trial aims to investigate the effects of physical exercise associated or not with taurine supplementation on intramuscular fat infiltration, physical performance, body composition, transcriptomic profile, and metabolomic profile in older women with obesity.

Forty women aged 60 to 75 years with obesity (Body mass index - BMI between 30 and 40 kg/m²) will be randomized into four groups:

  • Control group;
  • Exercise group;
  • Taurine supplementation group;
  • Exercise plus taurine supplementation group. The intervention will last 16 weeks. Participants allocated to exercise groups will perform supervised concurrent exercise training three times per week, including resistance and aerobic exercises. Participants allocated to taurine groups will receive 3 grams per day taurine supplementation.

Assessments performed before and after the intervention will include magnetic resonance imaging for intramuscular fat evaluation, body composition by dual-energy X-ray absorptiometry (DXA), muscle biopsy, blood biomarkers, indirect calorimetry, functional capacity tests, muscle strength, transcriptomic analysis, and metabolomic analysis.

This study may contribute to the development of innovative non-pharmacological strategies for obesity, aging, and intramuscular fat infiltration management.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female,
  • 60 and 75 years of age,
  • Body mass lower than 120 kg,
  • Be sedentary (not having engaged in physical exercise for at least 3 months), and
  • Body Mass Index between 30 and 40 kg/m².

Exclusion criteria

  • alcohol consumption,
  • smoking,
  • infectious and contagious diseases,
  • chronic kidney diseases,
  • undergoing weight loss treatment, and
  • presenting a score ≤13 on cognitive screening using the Mini-Mental State Examination (MMSE).

Treatment and study plan

Concurrent Exercise Training

Behavioral

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

Dietary Supplement

Participants will receive 3 grams per day taurine supplementation administered orally in capsules for 16 weeks.

Placebo

Other

Participants will receive placebo capsules identical in appearance to taurine capsules.

Primary outcomes

  1. Change from Baseline in Intramuscular Fat Fraction Assessed by Magnetic Resonance Imaging (Dixon Technique)

    Time frame: Baseline and 16 weeks

    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.

  2. Change from baseline in skeletal muscle transcriptomic profile

    Time frame: Baseline and 16 weeks

    Skeletal muscle biopsy samples will be analyzed using RNA sequencing to characterize changes in the skeletal muscle transcriptomic profile following the intervention.

  3. Change from baseline in plasma metabolomic profile

    Time frame: 16 weeks

    Plasma samples will be analyzed using untargeted metabolomic analysis to evaluate changes in the plasma metabolomic profile after 16 weeks of intervention.

  4. Change from baseline in plasma taurine concentration

    Time frame: Baseline and 16 weeks

    Plasma taurine concentration will be measured before and after the 16-week intervention.

Secondary outcomes

  1. Change from baseline in Timed Up and Go test time

    Time frame: Baseline and 16 weeks

    Functional mobility will be assessed using the Timed Up and Go test.

  2. Change from baseline in handgrip strength

    Time frame: Baseline and 16 weeks

    Handgrip strength will be assessed using a hand dynamometer.

  3. Change from baseline in chair stand test performance

    Time frame: Baseline and 16 weeks

    Lower-body functional performance will be assessed using the Chair Stand Test.

  4. Change from baseline in forearm flexion test performance

    Time frame: Baseline and 16 weeks

    Upper-body muscular endurance will be assessed using the Forearm Flexion Test.

  5. Change from baseline in isokinetic knee extensor peak torque

    Time frame: Baseline and 16 weeks

    Peak torque of the knee extensor muscles will be measured using an isokinetic dynamometer.

  6. Change from baseline in fat-free mass

    Time frame: Baseline and 16 weeks

    Fat-free mass will be assessed by dual-energy X-ray absorptiometry.

  7. Change from baseline in fat mass

    Time frame: Baseline and 16 weeks

    Fat mass will be assessed by dual-energy X-ray absorptiometry.

  8. Change from baseline in fasting blood glucose concentration

    Time frame: Baseline and 16 weeks

    Fasting blood glucose concentration will be measured using blood samples collected after an overnight fast.

  9. Change from baseline in fasting insulin concentration

    Time frame: Baseline and 16 weeks

    Fasting insulin concentration will be measured using blood samples collected after an overnight fast.

  10. Change from baseline in total cholesterol concentration

    Time frame: Baseline and 16 weeks

    Total cholesterol concentration will be measured using fasting blood samples.

  11. Change from baseline in high-density lipoprotein cholesterol concentration

    Time frame: Baseline and 16 weeks

    High-density lipoprotein cholesterol concentration will be measured using fasting blood samples.

  12. Change from baseline in low-density lipoprotein cholesterol concentration

    Time frame: Baseline and 16 weeks

    Low-density lipoprotein cholesterol concentration will be measured using fasting blood samples.

  13. Change from baseline in triglyceride concentration

    Time frame: Baseline and 16 weeks

    Triglyceride concentration will be measured using fasting blood samples.

  14. Change from baseline in resting metabolic rate

    Time frame: Baseline and 16 weeks

    Resting metabolic will be assessed by indirect calorimetry after an overnight fast.

Sponsors and collaborators

Lead sponsor

University of Sao Paulo

Other

Registry information

Official study title

The Impact of Physical Exercise Associated or Not With Taurine Supplementation on Intramuscular Fat Infiltration in Older Women With Obesity: A Transcriptomic and Metabolomic Approach

Acronym: TAUMUSCLE

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 28, 2026
Registry last updated
Jul 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.