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

NCT05726721 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 180

Last updated 2025-02-06

No results posted yet for this study

Summary

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.

Conditions

  • Binge-Eating Disorder
  • Emotion Regulation
  • Executive Dysfunction
  • Eating Behavior
  • Depressive Symptoms

Interventions

OTHER

Treatment as usual, Psychotherapy

The three treament sites will offer psychotherapy as usual. All including elements of cognitive behavioral therapy and some sites also additional elements from either narrative therapy or interpersonal therapy

Sponsors & Collaborators

  • Aalborg University Hospital

    collaborator OTHER

  • Kompetencecenter for Spiseforstyrrelser

    collaborator UNKNOWN

  • Aarhus University Hospital

    lead OTHER

Principal Investigators

  • Loa Clausen, PhD · Aarhus University Hospital, Psychiatry

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-03
Primary Completion
2027-12-30
Completion
2028-05-31

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05726721 on ClinicalTrials.gov