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Applying Social Comparison Theory to Behavioral Weight Loss: Does Modifying Group Membership Improve Outcome?

Not Applicable
Completed
Conditions
Obesity
Interventions
Behavioral: Standard behavioral treatment for weight loss
Behavioral: Modified behavioral treatment for weight loss
Registration Number
NCT00716027
Lead Sponsor
The Miriam Hospital
Brief Summary

The purpose of this study is to determine whether a modified behavioral treatment for weight loss that includes one-on-one treatment for individuals struggling to lose weight is associated with more weight loss than a standard behavioral treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
Inclusion Criteria
  • BMI between 27 and 45 kg/m2
Exclusion Criteria
  • participating in a weight loss program or taking a weight loss medication
  • currently pregnant, lactating, or less than 6-months post-partum or plan to become pregnant during the time of the intervention.
  • report a heart condition, chest pain during periods of activity or rest, or loss of consciousness
  • report conditions that would render the participant unlikely to follow the study protocol (e.g., terminal illness, relocation, substance abuse, sever psychiatric condition, dementia).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1Standard behavioral treatment for weight lossA 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity.
2Modified behavioral treatment for weight lossA 24-week intervention in which individuals will meet weekly to be instructed on behavioral change associated with weight loss, including modifying dietary intake, self-monitoring weight and eating behaviors, and increasing physical activity. In this intervention, individuals not meeting weight loss goals will be given one-on-one treatment.
Primary Outcome Measures
NameTimeMethod
weightweekly for 24-weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

The Miriam Hospital

🇺🇸

Providence, Rhode Island, United States

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