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Clinical Trial 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).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05993728
Study type Interventional
Source Oslo University Hospital
Contact Line Wisting, PhD
Phone +4793495268
Email uxwili@ous-hf.no
Status Recruiting
Phase N/A
Start date February 15, 2024
Completion date December 31, 2027

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