Exercise Effects on Adipose Tissue Structure and Function

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorUniversity of Michigan

About this trial

Participants will be randomized into one of two different experimental groups: 1) Exercise group and 2) No exercise (control group). Subject participation in the study will involve a series of metabolic tests before and after participants undergo a 10% weight loss program (with or without exercise training depending on group randomization). After completing this weight loss portion of the study, participants will then be required to adhere to a high calorie diet program to regain half of the weight the participant lost - followed by the same series of metabolic tests.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age: 18-40

Body Mass Index: 27-45 kg/m2

No regularly planned exercise/physical activity for at least 6 months

Women must have regularly occurring menses and must be premenopausal

Disqualifiers

Evidence/history of cardiovascular or metabolic disease

Medications known to affect lipid or glucose metabolism, or inflammation

Weight instability ≥ ± 6 pounds in the last 3 months

Tobacco or e-cigarette users

Trial design

Design model

Parallel

Treatments tested in this trial

  • Exercise

    Behavioral

    Participants will complete a moderate intensity continuous exercise 4 days/week.

  • No exercise

    Behavioral

    Participants will remain sedentary throughout the duration of the study.

Treatment groups

46 Participants
are divided into 2 treatment groups
Group A: ExerciseExperimental treatment 1 intervention
Group B: No exerciseExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Oral Glucose Tolerance Test (OGTT)

A test in which glucose is given and blood samples taken afterward to determine how quickly it is cleared from the blood will be completed at each clinical visit appointment..

Time frame
2 hours
2

Adipose Tissue Fibrosis

measured histologically using Sirus Red Staining, quantified using ImageJ software at each clinical visit appointment.

Time frame
30 minutes
3

Muscle Capillarization

measured immunohistochemically using an antibody for CD31, quantified using ImageJ software at each clinical visit appointment.

Time frame
30 minutes
4

Adipose Capillarization

measured immunohistochemically using an antibody for CD31, quantified using ImageJ software at each clinical visit appointment.

Time frame
30 minutes

Secondary outcomes

1

Blood Lipid Profile

A panel of blood tests that screens for abnormalities in blood lipids will be measured at each clinical visit appointment.

Time frame
15 minutes
2

Blood Pressure

The pressure of circulating blood against the walls of blood vessels will be measured at screening and each clinical visit appointment.

Time frame
10 minutes

Other outcomes

Sponsors and contacts

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