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N/A N=69 Randomized Single-blind Prevention

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

Eating Disorders

Enrolled (actual)
69
Serious AEs
0.0%
Results posted
Dec 2024
Primary outcome: Primary: Change Over Time in Body Dissatisfaction — .42; 0.51 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Peer Led Group Intervention (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
Stanford University
Primary completion
Mar 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Change Over Time in Body Dissatisfaction
.42; 0.51
PRIMARY
Change Over Time in Thin Ideal Internalization
-0.64; -0.59
SECONDARY
Change Over Time in Negative Affect
-0.17; -0.41
SECONDARY
Change Over Time in Dieting
-0.48; -0.77
SECONDARY
Body Comparison Orientation
-0.38; -0.60
SECONDARY
Change Over Time in Social Appearance Anxiety
SECONDARY
Change Over Time in Body Compassion
SECONDARY
Change Over Time in Self-Stigma of Seeking Help Scale
SECONDARY
Number of Eating Disorder Behaviors (Events) as a Measure of Change Over Time in Eating Disorder Symptoms
-5.22; -3.68
SECONDARY
Body Project Specific Attitude Measures
SECONDARY
Body Project Specific Outcome Measures

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.

Eligibility Criteria

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.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05794763). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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