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Clinical Trials/NCT00067873
NCT00067873
Completed
Not Applicable

Exercise Training in Obesity-prone Black and White Women

University of Alabama at Birmingham1 site in 1 country231 target enrollmentDecember 2000
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
University of Alabama at Birmingham
Enrollment
231
Locations
1
Primary Endpoint
Weight loss
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Overweight premenopausal Black and White women are randomized to either diet-only, diet+aerobic or diet+resistance exercise training. Diet/behavior intervention, with or without the aerobic or resistance exercise training, will be provided throughout the 18 months of study. Major outcomes will include measures of perceived and physiologic difficulty of exercise (cardiac, ventilatory, electromyographic responses to standardized exercise tasks); aerobic fitness; strength fitness; and spontaneous free-living energy expenditure (all derived from doubly labeled water). The results will provide insight into the effectiveness of, and the mechanisms by which, different types of exercise training can improve physical fitness, spontaneous engagement in physical activities of daily living and, in turn, weight-loss maintenance.

Detailed Description

Overweight premenopausal Black and White women are randomized to either diet-only, diet+aerobic or diet+resistance exercise training. Diet/behavior intervention, with or without the aerobic or resistance exercise training, will be provided throughout the 18 months of study. Major outcomes will include measures of perceived and physiologic difficulty of exercise (cardiac, ventilatory, electromyographic responses to standardized exercise tasks); aerobic fitness; strength fitness; and spontaneous free-living energy expenditure (all derived from doubly labeled water). The results will provide insight into the effectiveness of, and the mechanisms by which, different types of exercise training can improve physical fitness, spontaneous engagement in physical activities of daily living and, in turn, weight-loss maintenance. Time of initial weight loss was defined as the time needed to reach the goal of 25 kg/m2 BMI. The women will then be evaluated one year after this time and the amount of weight gain will be determined.

Registry
clinicaltrials.gov
Start Date
December 2000
End Date
December 2007
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Gary Hunter, PhD

Principle Investigator

University of Alabama at Birmingham

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Weight loss

Time Frame: 6 months

Change in weight after initial weight loss

Time Frame: 12 months after initial weight loss (maximum 18 months after randomization)

Time of initial weight loss determined by days to reach BMI \<= 25 (maximum 6 months)

Secondary Outcomes

  • Change in resting energy expenditure(18 months post baseline)
  • Insulin sensitivity(18 months post baseline)
  • Change in visceral fat(18 months post baseline)
  • Change in cholesterol(18 months post baseline)
  • Change in triglycerides(18 months post baseline)

Study Sites (1)

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