Structural Brain Volumetry Changes in Eating Disorders.
1 other identifier
observational
80
0 countries
N/A
Brief Summary
The goal of this observational study is to investigate the relationship between structural brain changes and psychiatric comorbidities in individuals diagnosed with eating disorders (EDs). The main question it aims to answer is: How are structural brain volumetric changes associated with psychiatric comorbidities in patients with eating disorders? Participants with a clinical diagnosis of an eating disorder will undergo brain MRI scans for volumetric analysis and structured psychiatric assessments to identify comorbid conditions. Data will be collected cross-sectionally from patients receiving routine clinical care, with the aim of identifying neurobiological and psychiatric patterns that could inform targeted treatment and prevention strategies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Dec 2025
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 13, 2025
CompletedFirst Posted
Study publicly available on registry
August 20, 2025
CompletedStudy Start
First participant enrolled
December 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 20, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 20, 2027
August 20, 2025
August 1, 2025
1.2 years
August 13, 2025
August 13, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
To assess structural changes of brain volumetry in patients with eating disorders and compare with healthy controls.
from enrollment till 18 months
Secondary Outcomes (1)
Highlight the extent of psychological disorders in such patients.
From enrollment till 18 months
Study Arms (4)
Anorexia Nervosa Patients
Bulimia Nervosa Patients
Binge-Eating Disorder
control group
Eligibility Criteria
Study Setting: in Assuit university hospitals, Neuropsychiatry hospital Outpatient Clinic Study subjects: will include three groups of patients with eating disorders: Anorexia nervosa patients, Bulimia Nervosa patients, Binge-eating patients, and healthy control group they will be age and sex matched.
You may qualify if:
- Age above 13 years.
- DSM-5 diagnosis of an eating disorder (AN, BN, BED) confirmed by structured interview.
You may not qualify if:
- Neurological or any previous psychiatric diagnosis.
- IQ less than 70.
- MRI contraindication (metal implants, pacemaker, severe claustrophobia).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Lecturer
Study Record Dates
First Submitted
August 13, 2025
First Posted
August 20, 2025
Study Start
December 10, 2025
Primary Completion (Estimated)
February 20, 2027
Study Completion (Estimated)
May 20, 2027
Last Updated
August 20, 2025
Record last verified: 2025-08