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Exercise Training in Obesity-prone Black and White Women

This study is currently recruiting patients.

Sponsored by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Information provided by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Purpose

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.

Condition Treatment or Intervention
Obesity
 Behavior: Diet
 Behavior: Exercise

MedlinePlus related topics:  Obesity

Study Type: Interventional
Study Design: Prevention, Randomized

Further Study Details: 

Expected Total Enrollment:  231

Study start: December 2000

Eligibility

Ages Eligible for Study:  21 Years   -   41 Years,  Genders Eligible for Study:  Female

Accepts Healthy Volunteers

Criteria


Location and Contact Information

Paul A Zuckerman, MA      205 934-4386    ZuckerP@shrp.uab.edu

Alabama
      University of Alabama at Birmingham, Birmingham,  Alabama,  35294,  United States; Recruiting
Gary R Hunter, PhD,  Principal Investigator

      University of Alabama at Birmingham, Birmingham,  Alabama,  35294,  United States; Recruiting
Paul A Zuckerman, MA  205-934-4386    Zuckerp@shrp.uab.edu 
David Bryan, MA  205 975-0269    dbryan@uab.edu 

More Information

Study ID Numbers:  BLKWHT
Record last reviewed:  August 2004
Record first received:  August 29, 2003
ClinicalTrials.gov Identifier:  NCT00067873
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2004-11-08
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