ACTIVE_NOT_RECRUITING

Preventing Disordered Eating and Body Dissatisfaction Among High-risk Pregnant Individuals

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Targeting Health and Resilience for Individuals With a Vulnerable Eating History (THRIVE)

Quick Facts

Study Start:2024-06-06
Study Completion:2026-04
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06659354

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Within the first or second trimester of pregnancy at enrollment
  2. 2. 18 years or older
  3. 3. Able to provide informed consent
  4. 4. Endorse a self-reported history of an eating disorder or disordered eating behaviors
  5. 5. Are willing and able to comply with all group and study procedures
  6. 6. English fluency and literacy
  1. 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. 2. Do not have access to a device with a camera

Contacts and Locations

Principal Investigator

Rachel Vanderkruik, PhD, MSc
PRINCIPAL_INVESTIGATOR
The Center for Women's Mental Health at Massachusetts General Hospital

Study Locations (Sites)

Massachusetts General Hospital
Boston, Massachusetts, 02114
United States

Collaborators and Investigators

Sponsor: Massachusetts General Hospital

  • Rachel Vanderkruik, PhD, MSc, PRINCIPAL_INVESTIGATOR, The Center for Women's Mental Health at Massachusetts General Hospital

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-06
Study Completion Date2026-04

Study Record Updates

Study Start Date2024-06-06
Study Completion Date2026-04

Terms related to this study

Keywords Provided by Researchers

  • Eating Disorder
  • Body Dissatisfaction
  • Body Image
  • Pregnancy

Additional Relevant MeSH Terms

  • Eating Disorders
  • Body Dissatisfaction