Brief Behavioral Weight Loss Treatment vs. Weight Watchers

Not Applicable

Completed

• Conditions: Obesity; Overweight

• Registration Number: NCT00249340
• Lead Sponsor: The Miriam Hospital

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.

Study Timeline

• Status Verified: 2005-08
• Study Start: 2005-11
• Study First Submitted: 2005-11-04
• Study First Submitted QC: 2005-11-04
• Study First Posted: 2005-11-07
• Study Completion: 2006-07
• Last Update Submitted: 2007-04-10
• Last Update Posted: 2007-04-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Weight Loss

Trial Locations

Locations (1)

Weight Control and Diabetes Research Center/The Miriam Hospital; 🇺🇸 Providence, Rhode Island, United States