Empowering mothers to prevent postpartum depression
Official title: The Effect of Stories to Empower Mothers Programme on Postpartum Depression in Primigravid Pregnant Women
Run by Ege University · NCT06787300 · Data updated 2026-11-12
This study is testing a new online program that helps first-time pregnant women use art to boost their mental health and reduce the risk of postpartum depression.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 30 (estimated) |
| Sponsor | Ege University Academic / other |
| Locations | 1 site (Izmir) |
| Status | Recruiting |
| Started | April 1, 2021 |
| Main results expected | June 10, 2025 |
| Study ends | November 2, 2025 |
| Registry record updated | January 22, 2025 |
| Trial ID | NCT06787300 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are first-time pregnant women between 24-32 weeks of gestation who have access to the internet and are willing to participate.
✕Probably not a fit
Patients who are in their first trimester, have psychiatric diagnoses, or face complications during pregnancy may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to develop and evaluate the 'Stories that Empower Mothers' program, designed to assess and enhance the mental health of first-time pregnant women. The program consists of six online sessions, focusing on the therapeutic power of art and psychiatric nursing principles to mitigate the risk of postpartum depression. Participants will be monitored through a quantitative, non-randomized experimental design with intervention and control groups, assessing their psychological resilience and postpartum depression risk. The study will involve pretest, posttest, and follow-up assessments to measure the program's effectiveness.
Why it matters
Potential benefit: If successful, this program could significantly reduce the incidence of postpartum depression among first-time mothers.
How similar studies have gone: Other studies have shown success with similar therapeutic approaches, indicating potential for positive outcomes in mental health interventions for pregnant women.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * First pregnancy, * Singleton pregnancy, * Gestational week between 24-32, * Regular doctor follow-up, * Scored ≥ 10 on the EDBS, * Scored \< 17 on the BDI, * Literate, * No disability in sensory organs that would prevent communication, * Owning a smart phone or computer, * Having internet access, * Volunteering Exclusion Criteria: * Being in the first trimester of pregnancy, * Being treated/therapized with any psychiatric diagnosis, * Having a risky pregnancy, * Being at risk of premature birth and developing it, * Having any complications related to pregnancy (gestational diabetes, hypertension, bleeding, etc.), * The baby is not healthy, * Developing complications during and after birth, * The baby needs intensive care after birth, * Having a baby lost, * Having a premature birth (\<37 weeks), * The mother has experienced serious daily life difficulties (disaster, loss, etc.), * Not attending three or more of the six sessions
Where it's running
-
Ege University
Izmir, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Ege M Topcu, Research Asst.
- Email: ege.miray.eyrenci@ege.edu.tr
- Phone: 05512030536
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Smartphone-supported single-session psychotherapy for postpartum depression
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-
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Postpartum Depression: A Digital Decision Support Tool for Providers
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Understanding how ketamine works for pain and depression after cesarean delivery
This study is testing how ketamine can help manage pain and depression in new mothers after a cesarean delivery compared to healthy men and women who are not pregnant.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.