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NCT Number: NCT05885971

Detection of Eating Disorders in Pregnant Women

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.

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Key information

Conditions

Eating Disorders Feeding and Eating Disorders Mental Disorders Pathological Conditions, Signs and Symptoms Pregnancy Related Signs and Symptoms Signs and Symptoms, Digestive

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Centre Hospitalier Henri Laborit

Poitiers, France

Location status: Recruiting

Location contact

Charlotte XAVIER-DAVID, MD

CONTACT

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

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

Treatment and study plan

Administration of the SCOFF-F and EDE-Q questionnaires

Diagnostic Test

The participants will answer to the SCOFF-F and EDE-Q questionnaires as well as socio-demographic questions

Primary outcomes

  1. Specific Eating Disorders items in pregnant women

    Time frame: 36 months

    A discriminant factor analysis will be used to study whether there are elements that can distinguish women with an Eating Disorders from those who do not have one during pregnancy.

Study contacts

Contact information is provided by the study sponsor or research team.

Charlotte XAVIER-DAVID

CONTACT

[email protected]

(0)5 49 52 34 93 ext. +33

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Henri Laborit

Other

Registry information

Acronym: PREGN'ED

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jun 2, 2023
Registry last updated
Jan 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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