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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00072917
Other study ID # OVOPOB DK62874 (complted)
Secondary ID DK62874
Status Completed
Phase N/A
First received November 12, 2003
Last updated January 15, 2010
Start date October 2003
Est. completion date June 2008

Study information

Verified date January 2010
Source National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date June 2008
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 25 Years to 35 Years
Eligibility - 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.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Colorado Health Sciences Center Denver Colorado

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

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