Progressive Metabolic Adaptations to Low Intensity Exercise Training and Weight Loss

Sponsor
University of Michigan (Other)
Overall Status
Completed
CT.gov ID
NCT01452074
Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
16
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36.6
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Study Details

Study Description

Brief Summary

the investigators first aim is to determine the effect of low intensity exercise (without weight loss) on insulin sensitivity, muscle lipid metabolism, and factors regulating these processes in skeletal muscle after 1 day, 2 wks, 12 wks of training, and again after 3 days without exercise in obese adults. the investigators second aim is to determine the effect of combining low intensity exercise training with 10% weight loss on insulin sensitivity, muscle lipid metabolism, and factors regulating these processes in skeletal muscle.

Although a single 40 minute session of exercise at a low exercise intensity will not improve insulin sensitivity, the investigators anticipate adaptations after two weeks of exercise training (6 session/wk; 12 session total) will improve insulin sensitivity and be accompanied by a reduction in fatty acid intermediates and a reduction in markers for pro-inflammatory activation in muscle. the investigators anticipate changes in insulin sensitivity, fatty acid partitioning, and pro-inflammatory markers the day after the last session of a 12 wk training program (without weight-loss) will be similar to that measured after 2 weeks of training. the investigators anticipate insulin sensitivity, accumulation of fatty acid intermediates, and pro-inflammatory activation will be markedly improved after 10% weight loss when measured the day after exercise. the investigators would expect the improvements in Insulin sensitivity, accumulation of fatty acid intermediates, and markers of inflammatory stress will be significantly attenuated when measured 3 days after the most recent exercise session, but beneficial effects of 10% weight loss on these metabolic endpoints will persist when compared with before weight loss.

Condition or Disease Intervention/Treatment Phase
  • Other: Exercise Training
  • Other: Weight Loss with continued Exercise Training
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
16 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Study Start Date :
Jul 1, 2011
Actual Primary Completion Date :
Jul 18, 2014
Actual Study Completion Date :
Jul 18, 2014

Arms and Interventions

Arm Intervention/Treatment
Other: Exercise Training with Weight Loss

During the first 12 weeks of the study, subjects will adhere to an exercise training program while maintaining their original body weight. The exercise training program will entail the following: 40min/session, ~50% of their maximal aerobic capacity (approximately 100-110 beats per min), 5-6 days/week After the first 12 weeks in the study, subjects will continue with the same exercise program, but then they will be placed on a reduced calorie diet until they lose exactly 10% of their original body weight

Other: Exercise Training
During the first 12 weeks of the study, subjects will adhere to an exercise training program while maintaining their original body weight. The exercise training program will entail the following: 40min/session, ~50% of their maximal aerobic capacity (approximately 100-110 beats per min), 5-6 days/week

Other: Weight Loss with continued Exercise Training
After the first 12 weeks in the study, subjects will continue with the same exercise program, but then they will be placed on a reduced calorie diet until they lose exactly 10% of their original body weight

Outcome Measures

Primary Outcome Measures

  1. Insulin Sensitivity [2-3 hours]

    A hyperinsulinemic-euglycemic clamp will be used to assess peripheral insulin sensitivity

Secondary Outcome Measures

  1. Resting Metabolic Rate [20-30 min]

  2. Meal Tolerance Test [2-3h]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • body mass index [BMI]: 30-45 kg/m2; All women must be pre-menopausal; Non-exerciser (no regularly planned exercise/physical activity)
Exclusion Criteria:
  • Hematocrit ≤ 34%; Fasting plasma glucose concentration ≥ 125 mg/dL; Weight instability ≥ ±5 lbs in past month; Taking medications known to affect lipid and/or glucose metabolism; evidence and/or history of cardiovascular or frank metabolic diseases; pregnancy or actively breast feeding

Contacts and Locations

Locations

Site City State Country Postal Code
1 Michigan Clincal Research Unit Ann Arbor Michigan United States 48109

Sponsors and Collaborators

  • University of Michigan
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Investigators

  • Principal Investigator: Jeffrey F Horowitz, University of Michigan

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jeffrey F Horowitz, Associate Professor, Movement Science, School of Kinesiology, University of Michigan
ClinicalTrials.gov Identifier:
NCT01452074
Other Study ID Numbers:
  • R01 DK077966 - PA
  • R01DK077966
First Posted:
Oct 14, 2011
Last Update Posted:
Mar 21, 2022
Last Verified:
Mar 1, 2022
Keywords provided by Jeffrey F Horowitz, Associate Professor, Movement Science, School of Kinesiology, University of Michigan
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 21, 2022