GLPwatch

Behavioral Therapy and GLP-1 Analogue Effects on Binge Eating, Weight, and Coping in Obesity

NCT07042672 · Recruiting

Last updated 2026-05-28

This clinical trial tests whether a combination of behavioral therapy and a GLP-1 medication helps adults with obesity and binge eating disorder manage their eating habits and weight over 12 months.

Status Recruiting Currently enrolling participants.
Type Observational
Participants 80 people Planned (estimated).
Who can join Ages 18–65 · all sexes
Timeline Started 2025-07 · est. completion 2028-12
Where 1 site · Norway

What this study is testing ClinicalTrials.gov NCT07042672 ↗

Description as written by the study sponsor.

This study is a clinical, longitudinal, non-randomized, prospective observational study that seeks to compare the treatment effects and safety of using GLP-1 analogues versus not using appetite suppressants during a lifestyle treatment program that includes individual consultations every fourth month and 10 weeks of CBT-E group therapy in patients with both obesity and BED. The primary objective of this study is to evaluate the impact on BED symptomatology, while the secondary objectives include examining the potential adoption of alternative harmful coping mechanisms. Additionally, the study will assess psychological well-being and weight changes and their consequent influence on obesity-associated comorbid conditions. Adult patients with coexisting obesity and BED presenting at the Obesity clinic at Haukeland University Hospital, Bergen, Norway, will be included Patients will be divided into two groups: Group-GLP1 (n = 40), who will use GLP-1 analogues, and Group-NoMED (n = 40), who will not use appetite suppressants. Both groups will otherwise follow the routine standardized patient care pathway with follow-up controls every four months and participation in CBT group therapy sessions. Changes in symptoms of BED, alternative harmful coping strategies and mental health will be recorded at baseline and 12 months using patient-reported questionnaires, as well as anthropometric and biochemical data.

Treatments tested

Main thing measuredChange in EDE-Q Global Score From Baseline to 12 Months
SponsorHaukeland University Hospital
Conditions studiedBinge Eating Disorder Associated With Obesity, Binge Eating Disorder, Eating Disorder Binge, Eating Disorders, GLP-1, CBT, Obesity &Amp; Overweight
GLP-1 drugs

Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT07042672 ↗