Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
61 participants
OBSERVATIONAL
2019-12-06
2021-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Interoceptive Nutritional Processing in Healthy Participants and Patients With Binge-Eating-Disorder
NCT04115852
Emotion Regulation in Binge Eating and Purging Among Adolescents
NCT03429114
fMRI and Ghlrein in Obesity and Binge Eating Disorder
NCT02038712
Neural Response to Food Stimuli: fMRI Changes Following Cognitive Behavioral Therapy for Binge Eating Disorder
NCT03604172
Comparing Neural Responses to Food Images in EDNOS Patients and Healthy Controls Using fMRI
NCT01882023
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Binge eating disorder (BED) patients
Individuals with BED diagnosis.
fMRI
(Imaging while) performing reward related tasks.
non-BED controls
Individuals that do not experience binges
fMRI
(Imaging while) performing reward related tasks.
subsyndromal BED controls
individuals that experience binges but do not fulfill the requirements for BED diagnosis.
fMRI
(Imaging while) performing reward related tasks.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
fMRI
(Imaging while) performing reward related tasks.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Subsyndromal binge eating (control)
Exclusion Criteria
* co-occurring psychotic, bi-polar disorders, alcohol/substance dependence within the past six months
* lack of capacity for consent
* medical disorders that would affect weight and ability to participate
* insufficient German language skills (assessment will be in German)
* taking medication that would affect weight
* irremovable metal attached to the body (e.g. piercings)
* irremovable medical devices (e.g. pacemakers)
* any trauma or surgery which may have left ferromagnetic material in the body
* large tattoos
* pregnancy
* claustrophobia
18 Years
69 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Else Kröner Fresenius Foundation
OTHER
University Hospital Tuebingen
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Nils B Kroemer, Dr
Role: PRINCIPAL_INVESTIGATOR
University Hospital Tuebingen
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Psychological Institute, University of Tübingen
Tübingen, Deutschland (deu), Germany
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
BEDVAR
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.