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Peer-Led Dissonance Eating Disorder Prevention: Virtual Delivery

Pilot Testing Virtual Delivery of the Body Project Eating Disorder Prevention Program

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04433247
Enrollment
75
Registered
2020-06-16
Start date
2020-03-03
Completion date
2021-05-31
Last updated
2021-09-28

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

Conditions

Eating Disorders

Keywords

Prevention, Peer Leader, Feeding and Eating Disorders

Brief summary

This proposed pilot study will 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 and negative affect), eating disorder symptoms, and future onset of eating disorders over 6-month follow-up in this population.

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. Although undergraduate peer-educator-led Body Project groups have produced larger reductions in outcomes than an eating disorder education video, an unmoderated Internet-based prevention program, and even clinician-led Body Project groups, it can be logistically difficult to schedule in-person Body Project groups with high school and college students. One solution to this key implementation barrier is to have peer educators deliver Body Project groups virtually over the Internet. A pilot trial in Sweden provided initial evidence that virtually-delivered peer-led Body Project groups produced greater reductions in eating disorder symptoms and future onset of eating disorders than an active expressive-writing intervention. The proposed pilot study will evaluate whether Body Project produces greater reductions in risk factor symptoms, eating disorder symptoms, and future onset of eating disorders in this population. Participation in the intervention will last four weeks. Participants will be randomly assigned to the intervention condition or waitlist-control condition. Assessments will take place at pre-intervention, post-intervention, and 6 month follow up. Waitlist control participants will receive the intervention after they complete their post-test assessment.

Interventions

Four week dissonance-based program wherein women with body image concerns complete verbal, written, and behavioral activities. The program consist of four 60-minute sessions.

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

Outcomes Assessor at post-test and 6 month follow-up are blind to participant randomization.

Eligibility

Sex/Gender
FEMALE
Age
16 Years to 26 Years
Healthy volunteers
Yes

Inclusion criteria

* Body image concerns

Exclusion criteria

* N/A

Design outcomes

Primary

MeasureTime frameDescription
Change over time in Body Dissatisfactionpre intervention obtained on intake, immediately post intervention, and 6-months after the conclusion of the interventionTen 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
Change over time in Thin Ideal Internalizationpre intervention obtained on intake, immediately post intervention, and 6-months after the conclusion of the interventionThe 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.

Secondary

MeasureTime frameDescription
Change over time in Negative Affectpre intervention obtained on intake, immediately post intervention, and 6-months after the conclusion of the interventionTwenty 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.
Change over time in Dietingpre intervention obtained on intake, immediately post intervention, and 6-months after the conclusion of the interventionThe 10-item Dutch Restrained Eating Scale will assess the frequency of dieting behaviors using a response scale ranging from 1 = never to 5 = always.
Change over time in Eating Disorder symptomspre intervention obtained on intake, immediately post intervention, and 6-months after the conclusion of the interventionInterviewer assesses frequency of eating disorder behaviors using Eating Disorder Diagnostic Interview

Countries

United States

Outcome results

None listed

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