Evaluation of Access to Screening for Post-partum Depression Via the Postnatal Interview Within 8 Weeks of Birth in Women Who Have Gave Birth at the Troyes Hospital ( DEPRESSIONPP )
NCT ID: NCT06469476
Last Updated: 2024-06-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
400 participants
OBSERVATIONAL
2024-03-01
2024-08-31
Brief Summary
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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.
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Detailed Description
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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
Conditions
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Study Design
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OTHER
RETROSPECTIVE
Interventions
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depression post partum
visit post partum
Eligibility Criteria
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Inclusion Criteria
* and agreeing to take part in the study.
* minors under the age of 18
* those protected by law (guardianship, curatorship and safeguard of justice)
* patients refusing to take part in the study
18 Years
FEMALE
Yes
Sponsors
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Centre Hospitalier de Troyes
OTHER
Responsible Party
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Principal Investigators
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Amjad KATTINI, DR
Role: PRINCIPAL_INVESTIGATOR
Centre Hospitalier de Troyes
Locations
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Centre Hospitalier de Troyes
Troyes, Grand Est, France
Countries
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Central Contacts
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Facility Contacts
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Stéphane Sanchez, MD
Role: primary
Other Identifiers
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2023-A02394-41
Identifier Type: -
Identifier Source: org_study_id
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