- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05930834
Exercise Training and Insulin Sensitivity
Exercise Training and Adipose Tissue Insulin Sensitivity
Regular exercise participation is known to reduce cardiometabolic disease risk but the impact that exercise training has on adipose tissue (AT) metabolism is poorly understood, particularly in humans. It is well established that exercise training improves whole-body glucose levels and increases insulin sensitivity, and this can occur within one or two weeks. These effects are usually due to adaptations in skeletal muscle, the tissue responsible for the majority of glucose disposal. However, many studies have now determined that exercise training also results in adaptations in AT that improve whole-body metabolic health by improving glucose uptake into the AT.
Skeletal muscle is thought to account for approximately 75-85% of glucose uptake , and this process is impaired in .individuals who are insulin-resistant state. It is postulated that the increased level of adiposity that accompanies severe obesity would result in higher dependency on AT for glucose uptake as the AT would be a bigger "sink". Thus the role of AT in inducing whole body insulin resistance is still unclear, particularly in individuals with obesity.
This study will examine the changes in AT glucose uptake before and after 4 weeks of exercise training in obese individuals and establish if there are sex differences.
Study Overview
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Alan Maloney, MS
- Phone Number: 989-954-3366
- Email: amzdr@mail.missouri.edu
Study Contact Backup
- Name: Jill Kanaley, PhD
- Phone Number: 573-882-2519
- Email: kanaleyj@missouri.edu
Study Locations
-
-
Missouri
-
Columbia, Missouri, United States, 65211
- University of Misouri
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- non-smokers, weight stable (<4 kg) within the last 6 months will be recruited for this study.
- sedentary (not engaged in planned physical activities and performing less than a total of 2 h of physical activity per week during the last 6 months) men and women whose BMI is classified as obese (>30 kg/m2).
Exclusion Criteria:
- cardiovascular disease, uncontrolled hypertension (no beta blockers), smokers, pregnant, have any recent changes in hormonal birth control, or on any medications known to impact metabolism.
- All participants will be regular sleepers with a duration of 7-9 hours/night.
- Subjects with orthopedic limitations will not be included.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Exercise
All subjects will undergo exercise training for 4 wks.
45-60 min of exercise, 4 sessions/wk supervised, 1 session unsupervised.
intensity 60% of VO2 max
|
All subjects will undergo exercise training for 4 wks.
45-60 min of exercise, 4 sessions/wk supervised, 1 session unsupervised.
intensity 60% of VO2 max
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
GLUT4 protein expression
Time Frame: 4 weeks
|
protein expression
|
4 weeks
|
TB1CD4 protein expression
Time Frame: 4 weeks
|
TB1CD4 protein expression
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
percent body fat
Time Frame: 4 weeks
|
Body fat will be measured using DEXA pre and post training
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jill Kanaley, University of Missouri-Columbia
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2096068
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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