Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
Healthy Volunteers
NCT06602141

Assessments of Adipogenesis, Lipid Turnover and Cellular Composition in Adipose Tissue in Response to Endurance Exercise

Led by AdventHealth Translational Research Institute · Updated on 2026-03-27

70

Participants Needed

2

Research Sites

237 weeks

Total Duration

On this page

Sponsors

A

AdventHealth Translational Research Institute

Lead Sponsor

P

Pennington Biomedical Research Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this research study is to study the effects of endurance exercise training on adipose (fat) tissue quality and insulin sensitivity in men and women.

CONDITIONS

Official Title

Assessments of Adipogenesis, Lipid Turnover and Cellular Composition in Adipose Tissue in Response to Endurance Exercise

Who Can Participate

Age: 18Years - 45Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Men and pre-menopausal women
  • Age 18 to 45 years
  • Body mass index (BMI) between 30.0 and 40.0 kg/m2
  • Women not using hormonal contraception must use specified birth control methods or abstain
  • Able to speak and understand English
  • Sedentary lifestyle with no more than 1 day per week of structured endurance or resistance exercise in the past year
  • Willing to be randomized to study groups
  • Willing to follow all study procedures
  • Signed informed consent and HIPAA authorization
Not Eligible

You will not qualify if you...

  • Unstable body weight (> ±5%) in the last 3 months
  • Significant recent changes in diet quality or physical activity
  • Weight over 396 pounds (180 kg)
  • Diagnosis of Type 1 or Type 2 diabetes
  • Fasting blood glucose ≥126 mg/dL or HbA1c ≥6.5%
  • Blood pressure over 140/90 mmHg
  • History of serious cardiovascular conditions or recent heart events
  • Anemia with low hemoglobin or hematocrit
  • Kidney disease or abnormal liver enzymes
  • Serious digestive disorders
  • Chronic infections or immune diseases requiring treatment
  • Current or past eating disorders
  • Bleeding or clotting disorders
  • Chronic obstructive pulmonary disease (COPD)
  • High triglycerides or LDL cholesterol
  • Recent blood donation or planned donation during study
  • Recent autoimmune treatment
  • Excessive alcohol consumption or recent smoking
  • Night shift work recently or planned
  • Allergy to local anesthetics
  • Thyroid disorders not stable
  • Prior bariatric or obesity surgery
  • Recent cancer treatment
  • Psychiatric conditions affecting study adherence
  • Pregnancy, recent postpartum or lactation, or planning pregnancy
  • Polycystic ovarian syndrome
  • Metabolic bone disease
  • Recent hospitalization for COVID-19
  • Partial or full hysterectomy
  • Unwillingness to provide biospecimens or undergo microdialysis
  • MRI contraindications or inability to tolerate MRI
  • Positive toxicology screen
  • Use of certain medications including recent changes or chronic treatments that interfere with study
  • Any condition compromising safety or data integrity per investigator judgment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

AdventHealth Translational Research Institute

Orlando, Florida, United States, 32804

Actively Recruiting

2

Pennington Biomedical Research Center

Baton Rouge, Louisiana, United States, 70808

Not Yet Recruiting

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Research Team

R

Recruitment Department

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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