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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06469476
Other study ID # 2023-A02394-41
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 1, 2024
Est. completion date August 31, 2024

Study information

Verified date June 2024
Source Centre Hospitalier de Troyes
Contact Stéphane Sanchez, DR
Phone 0325497561
Email recherche.clinique@hcs-sante.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Post-partum depression is defined as a depressive disorder with onset of symptoms in the year following childbirth. Several international studies have reported a prevalence of this condition of around pathology of around 15%. Santé publique France's 2021 national perinatal survey corroborated these figures, finding a prevalence of post-partum depression in France of in France of 16.7%. It is therefore a frequent pathology that can cause complications for both mother and child. The complications both for the mother and for the mother-child bond. Indeed, post-partum depression can lead to an increased risk of infanticide, weaker mother-child attachment, and altered parental behaviour. post-partum depression can lead to maternal suicide (the second leading cause cause of maternal mortality in France). Despite the potential seriousness of severe depression and its impact on the on the mother-child bond, just under half of those suffering from severe depression suffering from severe depression consult a healthcare professional. Fear of being judged or stigmatised, linked to misperceptions about the episode, is one of the main obstacles to consultation. Of being judged or stigmatised, linked to erroneous representations of the depressive episode. Given the scale of this condition, and the difficulties young mothers face in seeking help for young mothers to seek help, it is vital to screen postpartum women as widely and post-partum women as early as possible. In view of the extent of this condition and the difficulties young mothers have in seeking help for young mothers, it is vital to screen post-partum women as widely and as post-partum. With this in mind, from July 2022, a compulsory early post-natal interview has been introduced, designed to screen for postpartum depression.


Description:

Main objective: To evaluate the associated factors, in particular referral by a professional as a determinant of whether or not the 'compulsory' early interview. Secondary objective: To assess the economic, geographical and other factors associated and other factors associated with the compulsory early postnatal interview. Type of study: Observational, retrospective study. Population: Women who gave birth at the Centre Hospitalier de Troyes from July 2022 to October 2023. Assessment criteria : To be referred or not by a health professional during the early postnatal interview. Investigation plan: Send the information note and no objection to all eligible eligible women, together with the questionnaire and a T envelope to return the completed questionnaire. Inclusion criteria The study will include adult women who have given birth at the Centre hospitalier de Troyes between July 2022 and October 2023 and agreeing to take part in the study. Non-inclusion criteria The following will not be included in the study - minors under the age of 18 - those protected by law (guardianship, curatorship and safeguard of justice) - patients refusing to participate in the study


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date August 31, 2024
Est. primary completion date June 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion criteria: - The study will include adult women who have given birth at the Centre hospitalier de Troyes from July 2022 to October 2023 - and agreeing to take part in the study. non inclusion criteria - minors under the age of 18 - those protected by law (guardianship, curatorship and safeguard of justice) - patients refusing to take part in the study

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
depression post partum
visit post partum

Locations

Country Name City State
France Centre Hospitalier de Troyes Troyes Grand-Est

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier de Troyes

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measure if the patient is yes or not to be referred by a healthcare professional during the early postnatal interview. question 3 months
Secondary Measure the socio-economic status financial parameter 3 months
Secondary measure the declaration of a financial or non-financial obstacle financial parameter 3 months
Secondary measure the knowledge about post-partum depression question first contact 3 months
Secondary measure the knowledge about early post-natal interview. question 3 months
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