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Clinical Trials in Norway / NCT05993728
Active, not recruiting Not applicable

Virtual Body Project Groups Led by Peers Versus Clinicians

NCT05993728 · tracked via the Priya Life Science Norway tracker
Phase
Not applicable
Started
2024-02-15
Last updated
2025-12-12

Condition(s) studied

Eating DisordersBody Image

Investigational drug(s) / intervention(s)

Body ProjectPsychoeducational control

Body Project: The Body Project prevention program is a body acceptance program to promote a healthy body image and prevent eating disorder onset.

Psychoeducational control: Participants randomized to the educational control condition will receive videos addressing body image and eating disorders

Study summary

Eating disorders (EDs) are a group of illnesses associated with significant psychological and physiological consequences. Overall, only 20% of individuals with EDs receive treatment and treatment is effective for only about 25-35% for those who receive care. The development and implementation of effective prevention approaches for those at risk is therefore pivotal. The Body Project is the most effective ED prevention program for at-risk females according to meta-analyses, but reach has been limited since delivery has traditionally been in-person. Further research is warranted to examine cost-effective and easily accessible approaches to increase scalability and potential for broad implementation. With this application, the investigators therefore propose to examine the effectiveness of the Body Project in young females, a high-risk group, with the following main novel aspects: i) virtually-delivered Body Project groups to maximize reach; ii) peer-led versus clinician-led virtually-delivered Body Project groups; iii) the inclusion of objective measures to assess engagement of intervention targets (i.e., mediator).

Eligibility

Sex
FEMALE
Min age
16 Years
Max age
25 Years
Healthy volunteers
No
Inclusion Criteria: * Age 16-25 * Female identifying * Self-reported body image concerns Exclusion Criteria: * Ongoing eating disorder diagnosis requiring treatment or hospitalization

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Oslo University Hospital Oslo Norway

More Oslo University Hospital trials in Norway

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05993728 on ClinicalTrials.gov ↗ ← All trials in Norway