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Study Purpose:
The combination of caloric restriction and exercise is the most common first-line treatment for obesity-related disorders, yet we know very little about how these two very different treatments work together. A deeper understanding about mechanisms underlying the health benefits of adding exercise to a weight loss program will not only aid efforts to optimize more effective lifestyle interventions, but it can also uncover novel targets for the treatment/prevention of obesity-related diseases.
Although a reduction in body fat is the fundamental adaptation to weight loss, we know almost nothing about the effects that adding exercise has on structural and functional changes within fat tissue that may further enhance metabolic health. This is very important because many obesity-related metabolic health complications are tightly linked with abnormalities in abdominal fat tissue. We argue exercise-induced modifications in abdominal fat tissue will reveal persistent health benefits even if some weight is regained
Study Summary:
10% Weight Loss Phase - Subject participation in the study will involve a series of metabolic tests before, at midpoint, and after undergoing a 10% weight loss program (with or without exercise training depending on group randomization). During this, subjects will be randomized into one of two different experimental groups:
Follow-up Phase: After completing the metabolic testing post-weight loss, all study-related diet and exercise supervision will end and subjects will be free to make their own choices regarding diet and exercise/physical activity behavior. Subjects will then be asked to complete follow-up testing at 2-, 4- and 6- months post-weight loss.
Total involvement in the study for each subject will likely be about 10-13 months (4-7 months during weight loss phase, 6 months during follow-up phase).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Moderate Intensity Continuous Training (MICT) exercise group | Experimental | 45 minutes of continuous steady-state exercise at 70% maximal heart rate throughout the 10% weight loss phase of the study |
|
| No exercise (Control) | Experimental | to remain sedentary (no planned physical exercise) throughout the duration of the 10% weight loss phase of the study |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MICT Exercise | Behavioral | Subjects randomized into this group will complete a moderate intensity continuous exercise 4 days/week. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Insulin sensitivity | a hyperinsulinemic-euglycemic clamp will be used to quantify peripheral insulin sensitivity | 2 hours |
| Fatty acid turnover | stable isotope tracer infusion methods will be used to assess fatty acid turnover | 2 hours |
| Adipose tissue capillarization | measured immunohistochemically using an antibody for CD31, quantified using ImageJ software | 30 minutes |
| Adipose tissue fibrosis | measured histologically using Sirus Red Staining, quantified using ImageJ software | 30 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| Body weight change | Change in body weight will be assessed 6 months after completing the 10% weight loss intervention | 6 months |
| Body fat mass | Body fat mass will be measured by Dual Energy X-ray Absorptiometry (DEXA) |
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Inclusion criteria
Exclusion criteria
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Suzette M Howton | Contact | 734-647-9850 | suzetter@med.umich.edu |
| Name | Affiliation | Role |
|---|---|---|
| Jeffrey Horowitz, PhD | University of Michigan | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Michigan | Recruiting | Ann Arbor | Michigan | 48109 | United States |
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| ID | Term |
|---|---|
| D009765 | Obesity |
| D008659 | Metabolic Diseases |
| D024821 | Metabolic Syndrome |
| D007333 | Insulin Resistance |
| D015431 | Weight Loss |
| ID | Term |
|---|---|
| D050177 | Overweight |
| D044343 | Overnutrition |
| D009748 | Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
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| No Exercise (Control) | Behavioral | Subjects randomized into this group will remain sedentary throughout the duration of the study. |
|
| 30 minutes |
| 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 | 2 hours |
| D001835 |
| Body Weight |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D006946 | Hyperinsulinism |
| D044882 | Glucose Metabolism Disorders |
| D001836 | Body Weight Changes |