Virtual Body Project Groups Led by Peers or Clinicians
Effectiveness of the Body Project to Prevent Eating Disorders in Young Females at Risk: a Randomized Controlled Trial
This study tests whether young women aged 16-25 benefit more from virtual body image support groups led by peers or by clinicians to help prevent eating disorders.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 441 (estimated) |
| Ages | 16 Years to 25 Years |
| Sex | Female |
| Sponsor | Oslo University Hospital Academic / other |
| Locations | 1 site (Oslo) |
| Trial ID | NCT05993728 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of the Body Project, a prevention program for eating disorders, delivered virtually to young females aged 16-25. It compares the outcomes of peer-led groups versus clinician-led groups to determine which approach is more effective in addressing body image concerns. The goal is to enhance accessibility and scalability of the program, which has shown promise in preventing eating disorders but has been limited by traditional in-person delivery methods.
Who should consider this trial
Good fit: Ideal candidates for this study are females aged 16-25 who have self-reported body image concerns.
Not a fit: Patients currently diagnosed with an eating disorder requiring treatment or hospitalization will not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve body image and reduce the risk of eating disorders among young females.
How similar studies have performed: Previous studies have shown success with similar virtual interventions for eating disorders, indicating potential for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 16-25 * Female identifying * Self-reported body image concerns Exclusion Criteria: * Ongoing eating disorder diagnosis requiring treatment or hospitalization
Where this trial is running
Oslo
- Oslo University Hospital — Oslo, Norway (Recruiting)
Study contacts
- Principal investigator: Line Wisting, PhD — Oslo University Hospital
- Study coordinator: Line Wisting, PhD
- Email: uxwili@ous-hf.no
- Phone: +4793495268
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.