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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05885971
Other study ID # 2023-A00529-36
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 30, 2023
Est. completion date June 1, 2026

Study information

Verified date August 2023
Source Centre Hospitalier Henri Laborit
Contact Charlotte XAVIER-DAVID
Phone (0)5 49 52 34 93
Email charlotte.xavier-david@ch-poitiers.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date June 1, 2026
Est. primary completion date June 1, 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

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

Locations

Country Name City State
France Centre Hospitalier Henri Laborit Poitiers

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Henri Laborit

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Specific Eating Disorders items in pregnant women 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. 36 months
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