Clincosm LogoSign in Get a demo

PREGN'ED: Detection of Eating Disorders in Pregnant Women

Sponsor
Centre Hospitalier Henri Laborit (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05885971
Collaborator
(none)
50
Enrollment
2
Arms
36
Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Administration of the SCOFF-F and EDE-Q questionnaires
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Detection of Eating Disorders in Pregnant Women
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Jun 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Other: Group of pregnant women with eating disorder

Diagnostic Test: Administration of the SCOFF-F and EDE-Q questionnaires
The participants will answer to the SCOFF-F and EDE-Q questionnaires as well as socio-demographic questions
Other: Group of pregnant women with no eating disorder

Diagnostic Test: Administration of the SCOFF-F and EDE-Q questionnaires
The participants will answer to the SCOFF-F and EDE-Q questionnaires as well as socio-demographic questions

Outcome Measures

Primary Outcome Measures

  1. Specific Eating Disorders items in pregnant women [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Centre Hospitalier Henri Laborit

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Henri Laborit
ClinicalTrials.gov Identifier:
NCT05885971
Other Study ID Numbers:
  • 2023-A00529-36
First Posted:
Jun 2, 2023
Last Update Posted:
Jun 2, 2023
Last Verified:
May 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Feeding and Eating Disorders

Study Results

No Results Posted as of Jun 2, 2023