Exploring profiles in adults with binge eating disorder
Profiling the Dynamic of Binge Eating Disorder (BED): a Longitudinal Study Examining the Influence of Emotion Regulation, Executive Function, Eating Pattern on BED and Outcome (PRODY-BED)
This study is trying to see if different emotional and thinking patterns in adults with binge eating disorder can help predict how well they respond to treatment over time.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 180 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Aarhus University Hospital Academic / other |
| Locations | 3 sites (Aarhus, Central Jutland and 2 other locations) |
| Trial ID | NCT05726721 on ClinicalTrials.gov |
What this trial studies
This observational study aims to identify specific profiles in adults with binge eating disorder (BED) based on their emotion regulation, executive function, and additional eating pathology. It seeks to determine if these profiles can predict treatment outcomes and track remission rates over time. Participants will complete questionnaires before, during, and after treatment, including follow-ups at 6 and 12 months. The study will be conducted at three sites in Denmark, focusing on understanding the interplay of various factors contributing to BED.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older diagnosed with binge eating disorder who are seeking treatment.
Not a fit: Patients with severe psychiatric comorbidities, such as psychosis or severe cognitive impairment, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more personalized treatment approaches for individuals with binge eating disorder.
How similar studies have performed: Other studies have shown promise in identifying subgroups within eating disorders, suggesting that this approach may yield valuable insights.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18+, * diagnosed with Binge eating Disorder, * and offered treatment at on of the inclusion sites. Exclusion Criteria: * Severe psychiatric comorbidity (e.g. psychosis, severe developmental disorder, severe cogntive impairement)
Where this trial is running
Aarhus, Central Jutland and 2 other locations
- Aarhus University Hospital, Psychiaty — Aarhus, Central Jutland, Denmark (Recruiting)
- Aalborg University Hospital — Aalborg, Denmark (Not_yet_recruiting)
- Kompetencecenter — Copenhagen NV, Denmark (Recruiting)
Study contacts
- Principal investigator: Loa Clausen, PhD — Aarhus University Hospital, Psychiatry
- Study coordinator: Loa Clausen, PhD
- Email: loaclaus@rm.dk
- Phone: +4529119734
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.