Managing Obesity by Combining Behavioral Weight Loss and Commercial Approaches
NCT ID: NCT00827593
Last Updated: 2012-04-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
144 participants
INTERVENTIONAL
2008-11-30
2011-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Standard behavioral weight loss
University-based behavioral weight loss treatment
Standard behavioral weight loss treatment
Participants will receive 12 months of university-based behavioral weight loss treatment
Weight Watchers
Weight Watchers program
Weight Watchers
Participants will receive 12 months of Weight Watchers
Combined Treatment
University-based behavioral weight loss treatment followed by Weight Watchers
Combined Treatment
Participants will receive university-based behavioral weight loss treatment followed by Weight Watchers
Interventions
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Standard behavioral weight loss treatment
Participants will receive 12 months of university-based behavioral weight loss treatment
Weight Watchers
Participants will receive 12 months of Weight Watchers
Combined Treatment
Participants will receive university-based behavioral weight loss treatment followed by Weight Watchers
Eligibility Criteria
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Inclusion Criteria
* BMI between 27-50 kg/m2
* Written approval/consent from primary health care provider
Exclusion Criteria
* Currently participating in a weight loss program or taking weight loss medication.
* Participated in a weight loss program in the last year
* Took weight loss medication in the last 6 months.
* Participated in Weight Watchers in last 2 years.
* Lost \>=5% of body weight during 6 months prior to screening.
* Pregnant, lactating, less than 6 months postpartum, or plan to become pregnant during study time frame.
* Report conditions that in the judgment of the principal investigator would render them potentially unlikely to follow protocol for the 12 month study.
* Report a medical condition that would affect the safety and/or efficacy of a weight management program involving changes in diet and physical activity.
30 Years
65 Years
ALL
Yes
Sponsors
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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
NIH
Baruch College City University of New York
OTHER
Responsible Party
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Angela M Pinto
Assistant Professor of Psychology
Principal Investigators
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Angela M Pinto, PhD
Role: PRINCIPAL_INVESTIGATOR
Baruch College
Locations
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Baruch College
New York, New York, United States
Countries
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References
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Pinto AM, Fava JL, Hoffmann DA, Wing RR. Combining behavioral weight loss treatment and a commercial program: a randomized clinical trial. Obesity (Silver Spring). 2013 Apr;21(4):673-80. doi: 10.1002/oby.20044.
Other Identifiers
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070601
Identifier Type: -
Identifier Source: org_study_id
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