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Our long-term goal is to identify new insights about effective approaches to obesity management and related lifestyle changes in African Americans and about factors that enhance or limit the response to specific treatment approaches. Our primary interest is in "natural social support" from family members or friends. However, since not all individuals seeking obesity treatment desire or are able to name family members or friends to participate with them, we will also study the benefits of social support by creating a "team" condition among individuals recruited alone. Specific aims are to: 1. Recruit overweight or obese "index" participants together with 1 or 2 family members or friend co-participants who are also overweight or obese, for enrollment in a 2 year weight loss program; 2. Conduct a randomized comparison of the effects, on weight loss and related behavioral and clinical outcomes of the index participants, of involving both index and co-participants (Group A) in the counseling program with those obtained when co-participants are not directly involved (Group B); 3. Enroll otherwise eligible index participants who do not name co-participants in a parallel 2 year weight loss study; Conduct a randomized comparison of the effects, on weight loss and related behavioral and clinical outcomes of individual participants, of creating social support teams of unrelated individuals (Group C) with those obtained when no such teams are created (Group D). Primary hypotheses are that: 1. weight loss from 0 to 12 months and from 0 to 24 months will be significantly greater in Group A vs. Group B; 2. weight maintenance from 12 to 24 months will be significantly greater in Group A vs. Group B; 3. weight loss from 0 to 12 months and from 0 to 24 months will be significantly greater in Group C vs. Group D; 4. weight maintenance from 12 to 24 months will be significantly greater in Group C vs. Group D. Secondary analyses will compare the respective treatment and control groups on changes in diet, physical activity, and clinical CVD risk factor changes over time and will assess predictors of outcomes and cost-effectiveness.
Age
16 - 70 years
Sex
ALL
Healthy Volunteers
No
3401 Market Street, Suite 202
Philadelphia, Pennsylvania, United States
Start Date
August 1, 2002
Primary Completion Date
October 1, 2006
Completion Date
October 1, 2006
Last Updated
March 31, 2008
344
Estimated participants
Weight Management
BEHAVIORAL
Lead Sponsor
University of Pennsylvania
NCT07472881
NCT01143454
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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