Empowering mothers to prevent postpartum depression
The Effect of Stories to Empower Mothers Programme on Postpartum Depression in Primigravid Pregnant Women
NA · Ege University · NCT06787300
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
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Ege University (other) |
| Locations | 1 site (Izmir) |
| Trial ID | NCT06787300 on ClinicalTrials.gov |
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.
Who should consider this trial
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.
Not a fit: Patients who are in their first trimester, have psychiatric diagnoses, or face complications during pregnancy may not benefit from this study.
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 performed: Other studies have shown success with similar therapeutic approaches, indicating potential for positive outcomes in mental health interventions for pregnant women.
Eligibility criteria
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 this trial is running
Izmir
- Ege University — Izmir, Turkey (Türkiye) (RECRUITING)
Study contacts
- Study coordinator: Ege M Topcu, Research Asst.
- Email: ege.miray.eyrenci@ege.edu.tr
- Phone: 05512030536
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: Postpartum Depression, postpartum depression, pschiatric nursing, promotion of mental health, nursing intervention