NCT06844188

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
1 day until next milestone

Study Start

First participant enrolled

February 20, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 25, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2025

Completed
4 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 5, 2025

Completed
Last Updated

November 25, 2025

Status Verified

February 1, 2025

Enrollment Period

4 months

First QC Date

February 19, 2025

Last Update Submit

November 20, 2025

Conditions

Keywords

prenatal carecesarean sectionprenatal educationprimary cesarean

Outcome Measures

Primary Outcomes (1)

  • primary cesarean rate

    rates of cesarean

    1 year

Eligibility Criteria

Age18 Years - 50 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailspregnant
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

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)

Location

Study Officials

  • Alev esercan, M.D.

    Sanliurfa Education and Research Hospital

    STUDY DIRECTOR

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

Locations