Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
NCT05885971

Detection of Eating Disorders in Pregnant Women

Led by Centre Hospitalier Henri Laborit · Updated on 2026-01-13

50

Participants Needed

1

Research Sites

152 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Eating disorders (ED) are insufficiently detected and belatedly or not treated during pregnancy. There are many screening questionnaires for eating disorders in the literature, but we note the absence of a specific and validated tool for their screening during pregnancy, which would make it possible to differentiate maternal dietary concerns related to pregnancy from symptoms linked to a proven eating disorder. The main objective of the study is to evaluate which items of the Sick Control One stone Fat Food (SCOFF-F) and Eating disorders examination questionnaire (EDE-Q) questionnaires could be specific to an ED during pregnancy and not related to the simple state of pregnancy, by comparing the answers of pregnant women, for whom the diagnosis of ED has been made, to those of pregnant women without an ED.

CONDITIONS

Official Title

Detection of Eating Disorders in Pregnant Women

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult pregnant woman
  • Woman with current diagnosed Eating Disorders or without Eating Disorders
  • Having a good command of the French language
  • Having given their consent for their participation in the research
Not Eligible

You will not qualify if you...

  • Underage pregnant woman
  • Woman who does not have a good command of the French language.
  • Woman with past Eating Disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier Henri Laborit

Poitiers, France

Actively Recruiting

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Research Team

C

Charlotte XAVIER-DAVID

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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