Can a group program help pregnant women with eating disorder histories?
NCT ID NCT06659354
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a program called the Pregnant Body Project (PBP) for pregnant individuals who have had an eating disorder or disordered eating in the past. The program involves six weekly group sessions on Zoom to help challenge unhealthy body ideals. Researchers want to see if the program is feasible and acceptable, and if it can reduce body dissatisfaction and disordered eating during pregnancy and after birth.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pregnant Body Project (PBP) - a behavioral intervention adapted from The Body Project, delivered as 6 weekly group sessions via Zoom
- What this could lead to
- If it works, this could provide an effective way to prevent eating disorder symptoms and body dissatisfaction during pregnancy and postpartum.
- What could go wrong
- This is a small feasibility study (60 participants) testing whether the program is practical and acceptable, not yet whether it works. Results may not apply to all pregnant individuals with eating disorder histories.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2024
- Expected to finish
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Apr 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Within the first or second trimester of pregnancy at enrollment 2. 18 years or older 3. Able to provide informed consent 4. Endorse a self-reported history of an eating disorder or disordered eating behaviors 5. Are willing and able to comply with all group and study procedures 6. English fluency and literacy Exclusion Criteria: 1. A diagnosis of bipolar or psychotic disorder, active mania or psychosis or substance abuse, an active eating disorder (active eating disorder symptomology informed by the Screening, Brief Intervention, and Referral to Treatment for Eating Disorders (SBIRT-ED) tool and clinician discretion), being at immediate risk of self-harm 2. Do not have access to a device with a camera
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
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Other studies related to the condition(s) this trial covers.
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