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Targeting Health and Resilience for Individuals With a Vulnerable Eating History (THRIVE)
The investigators aim to conduct a feasibility randomized controlled trial (RCT) of an eating disorder prevention program (The Body Project, adapted for pregnancy) versus a health education control among pregnant individuals with histories of an ED. The investigators will test the feasibility, implementation outcomes, and its preliminary effectiveness in reducing the risk of elevated disordered eating and body dissatisfaction during pregnancy and postpartum.
The investigators aim to conduct a feasibility randomized controlled trial (RCT) of an eating disorder prevention program (The Body Project, adapted for pregnancy) versus a health education control among pregnant individuals with histories of an ED. The investigators will test the feasibility, implementation outcomes, and its preliminary effectiveness in reducing the risk of elevated disordered eating and body dissatisfaction during pregnancy and postpartum. The investigators will aim to recruit N=60 pregnant individuals (in their first or second trimester) with histories of an ED. Both the intervention and active control consist of 6, weekly, 1-hour group sessions (6-8 participants per group) delivered over Zoom. There are four assessment points: pre-intervention, post-intervention, 3 months postpartum, and 6 months postpartum. Participants will complete online surveys at each assessment point and a post-intervention exit interview (active intervention only).
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
No
Massachusetts General Hospital
Boston, Massachusetts, United States
Start Date
June 6, 2024
Primary Completion Date
April 1, 2026
Completion Date
April 1, 2026
Last Updated
November 17, 2025
60
ESTIMATED participants
Pregnant Body Project (PBP)
BEHAVIORAL
Pregnancy Health Education (PHE)
BEHAVIORAL
Lead Sponsor
Massachusetts General Hospital
NCT07422571
NCT06306586
NCT07179068
Data Source & Attribution
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