Resistance Training Effects on Gut Microbiome and Cardiometabolic Outcomes
- Conditions
- Exercise Intervention
- Interventions
- Other: Conventional physical activity guidelinesBehavioral: Resistance training
- Registration Number
- NCT04906525
- Lead Sponsor
- University of Missouri-Columbia
- Brief Summary
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.
- Detailed 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 34
- 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
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Conventional physical activity guidelines Conventional physical activity guidelines Participants are given recommendations on physical activity guidelines Resistance training Resistance training Participants will undergo 6 weeks of supervised resistance training
- Primary Outcome Measures
Name Time Method Change in stool microbiome composition Change over 6 weeks 16s rRNA sequencing
Change in stool microbiome diversity Change over 6 weeks 16s rRNA sequencing
- Secondary Outcome Measures
Name Time Method Fat mass Change over 6 weeks body composition
Sleep Quality change over 6 weeks Measured using actigraphs
24hr appetite ratings Once at baseline and at the end of 6 week intervention Subjective rating using visual analog scales
Change in Body mass change over 6 weeks Measured in kg
Hip circumference change over 6 weeks anthropometrics
Physical activity change over 6 weeks kcalories burned during free living activity measured by accelerometer
Change in blood pressure change over 6 weeks diastolic and systolic blood pressure
Fat free mass Change over 6 weeks body composition
Change in glucose regulation change over 6 weeks 2 hour glucose clearance
Sleep Duration change over 6 weeks Measured using actigraphs
Change in fasting glucose change over 6 weeks Fasting Glucose
Waist circumference change over 6 weeks anthropometrics
Short chain fatty acids Change over 6 weeks Acetate, propionate, and butyrate
Trial Locations
- Locations (1)
University of Missouri
🇺🇸Columbia, Missouri, United States