Retrospective Examination of Electroencephalography Signals of Individuals With Different Eating Disorders

NCT ID: NCT05555277

Last Updated: 2022-09-29

Study Results

Results pending

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.

Recruitment Status

COMPLETED

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-04-01

Study Completion Date

2022-09-09

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of this study was to investigate the difference between electroencephalography (EEG) data and current psychological status of individuals diagnosed with anorexia nervosa (AN) and bulimia nervosa (BN).

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The data used in this study were obtained from individuals aged 18 and younger with eating disorders who applied to Üsküdar University NP Istanbul Brain Hospital. Two different diagnostic groups, Anorexia Nervosa and Bulimia Nervosa, were included in the study. Demographic information, secondary diagnosis status, Beck Depression Inventory (BDI), Beck Anxiety Inventory (BAI), Eating Attitude Test - 40 (EAT-40) scores and EEG data were used to investigate the differences between eating disorders. Comparison of neurological differences between individuals with AN and BN was done retrospectively.

This information, which will be obtained for AN and BN, which are diseases in which severe deterioration in behavior and perception are seen, can give advice to experts in planning treatment and rehabilitation processes.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Anorexia Nervosa Bulimia Nervosa

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Anorexia Nervosa

Individuals aged 18 years and younger with anorexia nervosa who have beck depression inventory, beck anxiety inventory, eating attitude test-40 and EEG data in their patient file.

No interventions - retrospective data collection

Intervention Type OTHER

The differences between the two diagnoses were investigated by using the scale results and EEG data in the patient files.

Bulimia Nervosa

Individuals aged 18 years and younger with bulimia nervosa who have beck depression inventory, beck anxiety inventory, eating attitude test-40 and EEG data in their patient file.

No interventions - retrospective data collection

Intervention Type OTHER

The differences between the two diagnoses were investigated by using the scale results and EEG data in the patient files.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

No interventions - retrospective data collection

The differences between the two diagnoses were investigated by using the scale results and EEG data in the patient files.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Being diagnosed with anorexia nervosa or bulimia nervosa to the DSM-V diagnostic criteria
* 18 years and younger
* Having an EEG data

Exclusion Criteria

* Having an EEG data taken in a center other than NP Istanbul Brain Hospital
* Lack of "Beck Depression Inventory", "Beck Anxiety Inventory" and "Eating Attitude Test-40" scale values in the patient file
Minimum Eligible Age

11 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Uskudar University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Fatma Demir

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Fatma Demir

Role: PRINCIPAL_INVESTIGATOR

Research assistant

Alper Evrensel

Role: STUDY_CHAIR

Associate professor

Tuğçe Ballı Altuğlu

Role: STUDY_DIRECTOR

Assistant professor

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Fatma Demir

Üsküdar, İ̇stanbul, Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

UskudarUni1

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Neurobiology of Bulimia Nervosa
NCT04225221 COMPLETED PHASE2
Self-Control in Bulimia Nervosa
NCT04409457 COMPLETED NA