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Resistance Training Effects on Gut Microbiome and Cardiometabolic Outcomes

University of Missouri (MU) logo

University of Missouri (MU)

Status

Completed

Conditions

Exercise Intervention

Treatments

Behavioral: Resistance training
Other: Conventional physical activity guidelines

Study type

Interventional

Funder types

Other

Identifiers

NCT04906525
2054484

Details and patient eligibility

About

The overall objective of this study is to investigate the effects of resistance training on the gut microbiome and cardiometabolic outcomes in adults with overweight and obesity.

Full description

The overall objective of this study is to investigate the effects of resistance training on the gut microbiome and cardiometabolic outcomes in adults with overweight and obesity.

Enrollment

34 patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18-35 years
  • BMI: 25-45 kg/m2
  • Sedentary lifestyle
  • Consistent diet patterns
  • Weight-stable (<4 kg change over the last 3 mo)
  • Willingness to adhere to resistance training protocol and not change diet
  • Non-smoker >1 year or more

Exclusion criteria

  • Disabilities preventing adherence to resistance training protocol
  • Recent start of medications that affect metabolism or appetite
  • Antibiotics
  • Diabetes
  • Drug therapy for coronary artery disease, peripheral artery disease, congestive heart failure, or dyslipidemia
  • Uncontrolled hypertension and blood pressure ≥ 180/110
  • Gastrointestinal disease and/or bariatric surgery
  • Smoking
  • Illicit drug use
  • Pregnant or lactating individuals

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

34 participants in 2 patient groups

Conventional physical activity guidelines
Other group
Description:
Participants are given recommendations on physical activity guidelines
Treatment:
Other: Conventional physical activity guidelines
Resistance training
Experimental group
Description:
Participants will undergo 6 weeks of supervised resistance training
Treatment:
Behavioral: Resistance training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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