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Study identifier: NCT05726721 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Profiling the Dynamic of Binge Eating Disorder (PRODY-BED)

Condition: Binge-Eating Disorder · Emotion Regulation · Executive Dysfunction  ·  Sponsor: Aarhus University Hospital

PhaseN/A
Planned participants180
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this observational study is to explore if different and specific profiles can be identified in adults with binge eating disorder (BED) depending on their additional eating pathology, emotion regulation and executive functions. The main questions it aims to answer are: * Is there different and specific subgroups of patients with BED according to baseline profiles in emotion regulation, executive function and additional eating pathology (including restriction, chaotic eating, grazing and eating on external cues)? * Are subgroups of individuals with BED (based on identified profiles) associated with outcome at end of treatment and follow-up? * What is the trajectories in remission rates of specific symptom dimensions (eating disorder pathology, emotion regulation, executive function, and depressive symptoms) in individuals with BED and is there specific trajectory profiles in these dimensions? * Is early changes in specific symptom dimensions (eating pathology, emotion regulation, executive function, or depression) associated with outcome of BED? Participants will be asked to fill in questionnaires before treatment as usual, 10 weeks into treatment, at end of treatment and at 6- and 12-month follow-up.

This description comes directly from the study's public registry record.

Talk to the study team

Loa Clausen, PhD  ·  +4529119734  ·  loaclaus@rm.dk

Always discuss trial participation with your own doctor first.

Locations (3)

Aarhus University Hospital, PsychiatyAarhus, Central Jutland, DenmarkRecruiting
Aalborg University HospitalAalborg, DenmarkNot Yet Recruiting
KompetencecenterCopenhagen NV, DenmarkRecruiting

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Source record: clinicaltrials.gov/study/NCT05726721