Evaluating access to screening for postpartum depression in new mothers
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 )
Centre Hospitalier de Troyes · NCT06469476
This study looks at how different factors affect whether new mothers get screened for postpartum depression after giving birth at a hospital in Troyes.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 400 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Centre Hospitalier de Troyes (other) |
| Locations | 1 site (Troyes, Grand Est) |
| Trial ID | NCT06469476 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the factors influencing access to screening for postpartum depression among women who have given birth at the Centre Hospitalier de Troyes. It focuses on the role of professional referrals in determining whether women receive a compulsory early postnatal interview within eight weeks of childbirth. The study will analyze data collected from women who gave birth between July 2022 and October 2023, evaluating economic, geographical, and other associated factors. Participants will complete a questionnaire to provide insights into their experiences and access to care.
Who should consider this trial
Good fit: Ideal candidates for this study are adult women who have given birth at the Centre Hospitalier de Troyes during the specified time frame and are willing to participate.
Not a fit: Patients who are minors, under legal protection, or refuse to participate will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve early detection and treatment of postpartum depression, enhancing maternal and child health outcomes.
How similar studies have performed: Other studies have indicated the importance of early screening for postpartum depression, suggesting that this approach could yield beneficial results.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Troyes, Grand Est
- Centre Hospitalier de Troyes — Troyes, Grand Est, France (RECRUITING)
Study contacts
- Principal investigator: Amjad KATTINI, DR — Centre Hospitalier de Troyes
- Study coordinator: Stéphane Sanchez, DR
- Email: recherche.clinique@hcs-sante.fr
- Phone: 0325497561
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Depression, Postpartum, depression post partum