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Reduction of Abdominal Obesity and Insulin Resistance in Women

This study has been completed.
Study NCT00664495.   Last updated on April 22, 2008.   Information provided by Queen's University

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Descriptive Information Fields
Brief Title  Reduction of Abdominal Obesity and Insulin Resistance in Women
Official Title  Reduction of Abdominal Obesity and Insulin Resistance in Women
Brief Summary

The purpose of the study was to assess the effects of equivalent diet- or exercise-induced weight loss and related insulin resistance in abdominally obese women.

Detailed Description
Study Phase
Study Type  Interventional
Study Design  Treatment, Randomized, Parallel Assignment
Primary Outcome Measure  Abdominal Obesity [ Time Frame: 4 months ] [ Designated as safety issue: No ]
Insulin Resistance [ Time Frame: 4 Months ] [ Designated as safety issue: No ]
Secondary Outcome Measure 
Condition  Obesity
Intervention  Behavioral: Diet Weight Loss
Behavioral: Exercise Weight Loss
Behavioral: Exercise Without Weight Loss
MEDLINE PMIDs 15166299
Links
Recruitment Information Fields
Recruitment Status  Completed
Enrollment 
Start Date  April 1999
Completion Date December 2003
Eligibility Criteria 

Inclusion Criteria:

  • Premenopausal women

Exclusion Criteria:

  • Smokers and diabetics
Gender Female
Ages 20 Years to 50 Years
Accepts Healthy Volunteers Yes
Contacts ††
Location Countries  Canada
Administrative Information Fields
NCT ID  NCT00664495
Organization ID Ross 1999
Secondary IDs ††
Study Sponsor  Queen's University
Collaborators †† Canadian Institutes of Health Research (CIHR)
Investigators 
Principal Investigator:     Robert Ross, PhD     Queen's University    
Information Provided By Queen's University
Verification Date April 2008
First Received Date  April 21, 2008
Last Updated Date April 22, 2008

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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