Skip to content

Managing Obesity by Combining Behavioral Weight Loss and Commercial Approaches

Managing Obesity by Combining Behavioral Weight Loss and Commercial Approaches

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00827593
Enrollment
144
Registered
2009-01-23
Start date
2008-11-30
Completion date
2011-10-31
Last updated
2012-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Brief summary

The purpose of this study is to examine the effectiveness of 3 behavioral weight loss programs- Weight Watchers, university-based behavioral weight loss treatment, and a combined approach which includes university-based treatment followed by Weight Watchers.

Interventions

Participants will receive 12 months of university-based behavioral weight loss treatment

BEHAVIORALWeight Watchers

Participants will receive 12 months of Weight Watchers

Participants will receive university-based behavioral weight loss treatment followed by Weight Watchers

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
Baruch College City University of New York
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Age between 30-65 years * BMI between 27-50 kg/m2 * Written approval/consent from primary health care provider

Exclusion criteria

* Unable to walk 2 blocks without stopping. * 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.

Design outcomes

Primary

MeasureTime frame
weight loss3, 6, 12 months

Secondary

MeasureTime frame
cost-effectiveness12 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026