Skip to main content
Clinical Trials/NCT00249340
NCT00249340
Completed
Not Applicable

Comparison of a Brief Behavioral Weight Loss Intervention With the Weight Watchers Program

The Miriam Hospital1 site in 1 country60 target enrollmentNovember 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
The Miriam Hospital
Enrollment
60
Locations
1
Primary Endpoint
Weight Loss
Status
Completed
Last Updated
19 years ago

Overview

Brief Summary

The purpose of this study is to compare the effectiveness of Weight Watchers, brief behavioral treatment, and a combination treatment. We hypothesize that a combination treatment will achieve greater weight losses than Weight Watchers alone.

Detailed Description

Weight Watchers is a popular nonmedical commercial weight loss program. Recent studies suggest that people enrolled in Weight Watchers lose approximately 3-5 kg in 6 months of treatment. These outcomes are substantially lower than average weight losses achieved in 6 months if university/hospital-based standard behavioral treatment (approximately 10 kg). However, standard behavioral weight loss programs are expensive and have limited accessibility to most people seeking weight loss. Therefore, the purpose of the current study is to investigate whether enhancing Weight Watchers by adding an 8-week group-based behavioral weight loss program prior to participation in Weight Watchers will improve weight loss outcomes at 6 months. Comparison: 6 months of Weight Watchers vs. combination treatment (2 months of standard behavioral weight loss treatment followed by 4 months of Weight Watchers) vs. 2 months of standard behavioral treatment.

Registry
clinicaltrials.gov
Start Date
November 2005
End Date
July 2006
Last Updated
19 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Age 21-65 years BMI 27-45 kg/m2 Able to sign informed consent

Exclusion Criteria

  • Women who are pregnant, nursing, less than 6 months postpartum, or plan to become pregnant during course of study Individuals who report a medical condition that would affect the safety and/or efficacy of a weight management program involving dietary change and physical activity (e.g., heart disease, cancer) Individuals with major psychiatric illness that would interfere with protocol adherence Individuals who are currently participating in a weight loss program or taking weight loss medication or lost \>=5% of body weight during 6 months prior to screening Recent (within the past 12 months) participation in Weight Watchers

Outcomes

Primary Outcomes

Weight Loss

Study Sites (1)

Loading locations...

Similar Trials