The Effects of Overfeeding on Obesity-Prone (OP) and Obesity-Resistant (OR) Women

Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
Overall Status
Completed
CT.gov ID
NCT00072917
Collaborator
(none)
100
1
56
1.8

Study Details

Study Description

Brief Summary

This is a longitudinal cohort study of how the responses to a 3 day period of controlled overfeeding relate to subsequent weight gain. We hypothesize that thin individuals are resistant to weight gain because they respond to periods of overfeeding by increasing fat oxidation, reducing food intake, and increasing physical activity relative to those who gain weight over time.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The Effects of Overfeeding on Obesity-Prone (OP) and Obesity-Resistant (OR) Women
    Study Start Date :
    Oct 1, 2003
    Study Completion Date :
    Jun 1, 2008

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      25 Years to 35 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      • Half of the subjects will be women, half will be men,

      • age 25-35,

      • a range of BMI's from 19-27, for the 'thin subjects' there should be no 1st degree relatives with a BMI>30.

      • Subjects should not engage in planned physical activity more than 3 hrs per week.

      • For the obesity prone group there should be at least 1 1st degree relative with a BMI>30.

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 University of Colorado Health Sciences Center Denver Colorado United States 80262

      Sponsors and Collaborators

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

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00072917
      Other Study ID Numbers:
      • OVOPOB DK62874 (complted)
      • DK62874
      First Posted:
      Nov 14, 2003
      Last Update Posted:
      Jan 18, 2010
      Last Verified:
      Jan 1, 2010

      Study Results

      No Results Posted as of Jan 18, 2010