Impact of Continuous Midwifery Care on Birth Outcomes
The Effect of the Education Given to Primiparous Pregnant Women Within the Framework of the Continuous Midwifery Care Model on Their Fears of Birth, Birth Preferences and Postpartum Trauma Perceptions.
This study tests if continuous care from midwives can improve birth experiences and health outcomes for first-time mothers and their babies.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 80 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | Female |
| Sponsor | Tarsus University Academic / other |
| Locations | 1 site (Mersin) |
| Trial ID | NCT06020339 on ClinicalTrials.gov |
What this trial studies
This project evaluates the effects of a midwife-led continuous care model on birth outcomes for pregnant women. It aims to address the limitations of current pregnancy and postpartum care by providing comprehensive support and education to first-time mothers. The study will involve 80 participants, divided into an experimental group receiving midwifery care and a control group. By focusing on improving the birthing experience and reducing cesarean rates, the research seeks to enhance maternal and neonatal health outcomes.
Who should consider this trial
Good fit: Ideal candidates are first-time pregnant women aged 18-35, residing in Mersin-Tarsus, who have no complications that would prevent vaginal delivery.
Not a fit: Patients with high-risk pregnancies or those requiring cesarean deliveries may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to improved birth experiences and lower cesarean section rates for pregnant women.
How similar studies have performed: Other studies have shown positive outcomes with midwifery-led care models, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Pregnant women who have completed at least primary education, * Able to speak, understand and write Turkish, * Pregnant women between the ages of 18-35 (pregnant women under 18 and over 35 years of age will not be preferred since they are among the risky groups in terms of maternal and fetal) * Pregnant women residing within the borders of Mersin-Tarsus * Primigravidas (It is planned to include primigravidas in the study, considering that there may be different variables affecting the fear of childbirth in previous pregnancies of multiparas.) * Pregnant women who do not have any obstacles to give vaginal birth * Pregnant women with a single and healthy fetus will be included in the study. Exclusion Criteria: * Pregnant women with any risky pregnancy history (preeclampsia, placenta previa, gestational diabetes mellitus, oligohydramnios and polyhydramnios, etc.), * Pregnant women with systemic and/or neurological disease, * Pregnant women with cesarean indication, * Pregnant women with chronic and/or psychiatric health problems (based on self-report and clinical diagnosis), * Pregnant women who participated in any childbirth preparation training program
Where this trial is running
Mersin
- Tarsus University — Mersin, Turkey (Recruiting)
Study contacts
- Study coordinator: Özlem KOÇ, Dr
- Email: ozlemkoc@tarsus.edu.tr
- Phone: +90 0552 083 95 94
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.