MedPath

The Body Project: Comparing the Effectiveness of an In-person and Virtually Delivered Intervention.

Not Applicable
Completed
Conditions
Eating Disorders
Interventions
Behavioral: Peer Led Group Intervention
Registration Number
NCT05794763
Lead Sponsor
Stanford University
Brief Summary

This present study will compare the efficacy of in-person versus virtually-delivered Body Project groups. It will also evaluate whether this body acceptance class produces greater reductions in eating disorder risk factor symptoms (pursuit of the thin ideal, body dissatisfaction, dieting, dietary restraint, negative affect, eating disorder symptoms, and the future onset of eating disorders over a 3-month follow-up in this population. It will also evaluate the effectiveness of this body acceptance class's ability to impact social appearance anxiety, body compassion, and self-stigma surrounding attaining help.

Detailed Description

Dozens of eating disorder prevention programs have been evaluated, but only the 4-hr Body Project has reduced eating disorder symptoms and future eating disorder onset over 3-4 year follow-up, produced larger reductions in outcomes than credible alternative interventions, been shown to engage the intervention target (valuation of the thin beauty ideal), and produced effects in trials from several independent teams. The proposed study will evaluate the effectiveness of a peer-implemented, virtually delivered, body acceptance class compared to a peer-implemented, in-person delivery of the same class. Participation in the intervention will last four weeks. Participants will be randomly assigned to the in-person or virtual body acceptance class. Assessments will take place at pre-intervention, post-intervention, and 3-month follow-up.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
69
Inclusion Criteria

Participants had to express body image concerns and all gender identities besides cisgender and transgender men were eligible.

Exclusion Criteria
  • Cisgender and transgender men were excluded due to the fact that The Body Project is typically administered with groups of all cisgender women.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Body Project: Virtual DeliveryPeer Led Group InterventionIn the virtual peer-led group intervention held over Zoom, participants voluntarily engage in verbal, written, and behavioral exercises in which they critique and discuss the costs of pursuing the thin-ideal ideal. The intervention is 4 sessions long (1-hr each) and is administered by trained peer facilitators who use an intervention script. Participants will be asked to complete weekly home exercises throughout the course of the intervention.
Body Project: In Person DeliveryPeer Led Group InterventionIn the in-person peer-led group intervention, participants voluntarily engage in verbal, written, and behavioral exercises in which they critique and discuss the costs of pursuing the thin-ideal ideal. The intervention is 4 sessions long (1-hr each) and is administered by trained peer facilitators who use an intervention script. Participants will be asked to complete weekly home exercises throughout the course of the intervention.
Primary Outcome Measures
NameTimeMethod
Change Over Time in Body DissatisfactionPre intervention obtained on intake, and immediately post intervention (after completion of 4 weeks of group session once a week)

Ten items from the Satisfaction and Dissatisfaction with Body Parts Scale assessed satisfaction with body parts with a response scale ranging from 1 = extremely dissatisfied to 6 = extremely satisfied. The mean score across the items is reported. Overall scores can range from 1 to 6 and a higher score indicate a greater level of body satisfaction.

Change Over Time in Thin Ideal InternalizationPre intervention obtained on intake, and immediately post intervention (after completion of 4 weeks of group session once a week)

The eight-item Ideal-Body Stereotype Scale-Revised will assess endorsement of the thin beauty ideal using a response scale ranging from 1 = strongly disagree to 5 = strongly agree. The mean score across the items is reported. Overall scores can range from 1 to 5 and a higher score indicates a greater level of thin ideal internalization.

Secondary Outcome Measures
NameTimeMethod
Change Over Time in Negative AffectPre intervention obtained on intake, and immediately post intervention (after completion of 4 weeks of group session once a week)

Twenty items from the sadness, guilt, and fear/anxiety subscales from the Positive Affect and Negative Affect Scale-Revised will assess negative affect. Participants reported the extent to which they had felt negative emotions on scales ranging from 1 = very slightly or not at all to 5 = extremely. The mean score across the items is reported. Overall scores can range from 1 to 5 and a higher score indicates a greater level of negative affect.

Change Over Time in DietingPre intervention obtained on intake, and immediately post intervention (after completion of 4 weeks of group session once a week)

The 10-item Dutch Restrained Eating Scale will assess the frequency of dieting behaviors using a response scale ranging from 1 = never to 5 = always. The mean score across the items is reported. Overall scores can range from 1 to 5 and a higher score indicates greater frequency of dieting behaviors.

Body Comparison OrientationPre intervention obtained on intake, and immediately post intervention (after completion of 4 weeks of group session once a week)

The six selected items from the Body, Eating, and Exercise Comparison Orientation Scale will assess the frequency of body comparisons using a response scale ranging from 1 = strongly disagree to 5 = strongly agree. The mean score across the items is reported. Overall scores can range from 1 to 5 and a higher score indicates greater frequency of body comparison.

Change Over Time in Social Appearance AnxietyPre intervention obtained on intake, and immediately post intervention.

The 16-item Social Appearance Anxiety Scale will assess levels of social appearance anxiety using a response scale ranging from 1 = not at all to 5 = extremely.

Change Over Time in Body CompassionPre intervention obtained on intake, and immediately post intervention.

The 10-item Body Appreciation Scale-2 will assess levels of body compassion using a response scale ranging from 1 = never to 5 = always.

Change Over Time in Self-Stigma of Seeking Help ScalePre intervention obtained on intake, and immediately post intervention.

The 10-item Self-Stigma of Seeking Help Scale will assess participants' views towards seeking help using a scale ranging from 1 = strongly disagree to 5 = strongly agree.

Body Project Specific Attitude MeasuresPre intervention obtained on intake, and immediately post intervention.

7 items assessing attitudes that are targeted as part of The Body Project training using a response scale ranging from 1 = strongly disagree to 5 = strongly agree.

Body Project Specific Outcome MeasuresPre intervention obtained on intake, and immediately post intervention.

7 items assessing attitudes that are targeted as part of The Body Project training using a response scale ranging from 1 = strongly disagree to 5 = strongly agree.

Number of Eating Disorder Behaviors (Events) as a Measure of Change Over Time in Eating Disorder SymptomsPre intervention and 3 months after the end of the intervention.

Interviewer assesses frequency of eating disorder behaviors using Eating Disorder Diagnostic Interview.

Trial Locations

Locations (2)

St. Mary's College of Maryland

šŸ‡ŗšŸ‡ø

Saint Marys City, Maryland, United States

Stanford University

šŸ‡ŗšŸ‡ø

Palo Alto, California, United States

Ā© Copyright 2025. All Rights Reserved by MedPath