Trauma Exposure, Emotion Regulation and Eating Pathology in Obese Patients

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

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-01-31

Study Completion Date

2017-05-31

Brief Summary

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

The purpose of this study is to investigate the associations between lifetime exposure to traumatic events, emotion regulation strategies, and eating pathology of patients with obesity.

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.

Obesity

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Trauma exposure Psychological distress Emotion regulation Mindfulness Eating pathology

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

CROSS_SECTIONAL

Eligibility Criteria

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

Inclusion Criteria

* Adults
* Obese (BMI \>= 30)
* Recruited from the nutrition service of Hôpital Européen Georges-Pompidou
* Informed consent provided

Exclusion Criteria

* PTSD symptoms (score \> 33 ; PTSD Checklist-5)
* Bariatric surgery patients
* Difficulties to understand French language
* Patients under social protection

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Responsible Party

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

Ruffault Alexis

Doctoral candidate

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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

Cécile Flahault, PhD

Role: STUDY_DIRECTOR

University Paris 5 - Rene Descartes

Sébastien Czernichow, Pr

Role: PRINCIPAL_INVESTIGATOR

University Paris 5 - Rene Descartes

Locations

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

Hopital Europeen Georges Pompidou

Paris, , France

Site Status

Countries

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

France

Other Identifiers

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

EA4057-troma

Identifier Type: -

Identifier Source: org_study_id