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The Effect of Prenatal Education on Primary Cesarean Rate

The Effect of Prenatal Education at Pregnancy School on Primary Cesarean Rate

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06844188
Enrollment
1000
Registered
2025-02-25
Start date
2025-02-20
Completion date
2025-07-05
Last updated
2025-11-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean Delivery Affecting Fetus, Prenatal Care Late

Keywords

prenatal care, cesarean section, prenatal education, primary cesarean

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.

Detailed description

Inclusion Criteria: All women who gave birth between January 2024 and December 2024 and attended antenatal classes (pregnancy school) 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. Exclusion Criteria: 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.

Interventions

None listed

Sponsors

Sanliurfa Education and Research Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

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.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frameDescription
primary cesarean rate1 yearrates of cesarean

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026