The Effect of Prenatal Education on Primary Cesarean Rate
1 other identifier
observational
1,000
1 country
1
Brief Summary
This is a prospective case-control study examining the impact of antenatal education on mode of delivery. The study will include all deliveries occurring between January 2024 and December 2024. Participants will be divided into two groups: a case group consisting of women who attended antenatal classes (pregnancy school) and a control group of women who did not. The primary outcome will be mode of delivery (vaginal or cesarean). The study will collect data on gravida and parity. Participants will be further categorized into four groups based on their delivery history: Women undergoing a cesarean section for their first delivery. Women experiencing a normal vaginal delivery for their first delivery. Women with a history of vaginal delivery who have another vaginal delivery in this pregnancy. Women with a history of vaginal delivery who deliver via cesarean section in this pregnancy. Each of these four groups will have a corresponding case (antenatal class attendees) and control (non-attendees) subgroup. Data on cesarean section indications, the name of the physician performing the cesarean, and the hospital's annual primary cesarean section rates will be requested from the hospital and compared across groups. For the case group, information regarding the specific antenatal education received, the gestational week at which the education was received, and patient characteristics such as age, infant birth weight, and educational level will also be collected.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 19, 2025
CompletedStudy Start
First participant enrolled
February 20, 2025
CompletedFirst Posted
Study publicly available on registry
February 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 5, 2025
CompletedNovember 25, 2025
February 1, 2025
4 months
February 19, 2025
November 20, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
primary cesarean rate
rates of cesarean
1 year
Eligibility Criteria
pregnant women of prenatal educated and prenatal non-educated about birth
You may qualify if:
- All women who gave birth between January 2024 and December 2024 and attended antenatal classes (gebe okulu) will be included in the study.
- For the control group (women who did not attend antenatal classes), participants will be randomly selected, matching the case group (antenatal class attendees) in terms of age, education level, and parity.
You may not qualify if:
- Women with a history of previous cesarean sections who are undergoing a repeat cesarean in this pregnancy will be excluded.
- Women with high-risk pregnancies, such as preeclampsia, preterm labor, preterm premature rupture of membranes, multiple pregnancies, previous cesarean section, or placental abruption, will not be included in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sanliurfa Training and Resarch Hospital
Sanliurfa, Turkey (Türkiye)
Study Officials
- STUDY DIRECTOR
Alev esercan, M.D.
Sanliurfa Education and Research Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 5 Months
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 19, 2025
First Posted
February 25, 2025
Study Start
February 20, 2025
Primary Completion
July 1, 2025
Study Completion
July 5, 2025
Last Updated
November 25, 2025
Record last verified: 2025-02