RecruitingNot ApplicableNCT06602141

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


Sponsor

AdventHealth Translational Research Institute

Enrollment

70 participants

Start Date

Sep 11, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Accelerometer, a procedure called Adipose Biopsy, and others for people with obesity. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 18 Years to 45 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREMuscle Biopsy

This procedure is used to sample muscle cells from the leg Vastus Lateralis (thigh) muscle.

PROCEDUREAdipose Biopsy

This procedure is used to sample fat tissue from the abdomen (belly).

OTHERGlucose Clamp

In this test, we will measure the effect of insulin by giving you insulin and glucose (sugar) intravenously through an IV line in your arm.

OTHERAccelerometer

The tri-axial accelerometer measure activity and uses those values to estimate the number of calories burned based on your height, weight, age, and gender. The monitor also evaluates physical effort and the body's response to different activities.

OTHEREndurance Exercise

Visit the study site 3 times a week to engage in endurance exercise training for approximately 12 weeks. Each session will last approximately 75 minutes, and exercise group can choose to use either a stationary bike or a treadmill to complete the training.

OTHERPhysical activity/ dietary habits

Visit the study site bi-weekly to get weight measurements and speak to the study team about weight maintenance and participant physical activity/dietary habits.

OTHERHeavy Water Labeling Period

Participants in both control groups will be required to drink heavy water, which is ordinary water that is enriched with deuterium (stable, non-radioactive isotope) and called deuterium-labeled water, for 12 weeks.


Locations(2)

AdventHealth Translational Research Institute

Orlando, Florida, United States

Pennington Biomedical Research Center

Baton Rouge, Louisiana, United States

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NCT06602141


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