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Life sciences · Interventional Study
ClinicalTrials.gov · October 30, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07301541). This is a study registration, not published results. Lead sponsor: University of Aarhus. Recruitment status: NOT_YET_RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 200 participants (ESTIMATED). Conditions: Binge Eating Disorder, Binge Eating, Loss of Control Eating, Overweight , Obesity, Children, Childhood Obesity, Screening, BED. Interventions: BEHAVIORAL: A 10-week multicomponent camp intervention for children; BEHAVIORAL: A BED intervention for parents. Primary outcome measures: Changes in Binge eating behavior using the STOB-screening tool , Baseline, 10-weeks (post-intervention), 10-12 weeks after the intervention, and 1, 3 and 5 years after the intervention.; Changes in prevalence of Binge eating disorder (BED) using the ChEDE , Baseline. Brief summary: The main purpose is to investigate the effectiveness of a 10-week multicomponent camp intervention to reduce BE behavior in children and adolescents and explore in a randomized controlled setting if a parent-based BED-intervention has any add-on effect, attenuating the development of BE behavior in this sample. The study will include an initial follow-up assessment scheduled 10-12 weeks after camp completion and plans for long-term follow-up assessments one, three and five years after inclusion. Overall, we hypothesize that the multicomponent camp intervention will effectively reduce BE behavior in children and adolescents. Furthermore, we hypothesize that participants whose parents are randomized to receive the parental BED intervention will show a lower prevalence of BE behavior one year after the camp intervention compared with children whose parents receive standard care.