Detection of Eating Disorders in Pregnant Women

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorCentre Hospitalier Henri Laborit

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

Underage pregnant woman

Woman who does not have a good command of the French language.

Woman with past Eating Disorders

Trial design

Design model

Parallel

Treatments tested in this trial

  • 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

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Group of pregnant women with eating disorderOther 1 intervention
Group B: Group of pregnant women with no eating disorderOther 1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
36 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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