Effects of Antenatal Education on Birth Perception, Fear, and Readiness (EA-BPFR)

March 24, 2025 updated by: Şahika ŞİMŞEK ÇETİNKAYA, Kastamonu University

The Effect of Antenatal Education Based on Transformative Learning Theory on Traumatic Birth Perception, Fear of Birth, and Birth Readiness in Pregnant Women: a Randomized Controlled Trial

Birth is a multi-dimensional and unique experience for every woman, and it is influenced by a woman's social life. Fear of childbirth is a common issue that affects women's health and well-being before, during, and after pregnancy. The thought that childbirth will be painful triggers fear of childbirth. Fear of childbirth is closely related to the perception of traumatic birth. Antenatal education is important in coping with childbirth pain and traumatic birth pain, but the aim of adult education is not just to inform, but also to change individuals' perspectives on events. The transformative learning theory is a model used to change individuals' perspectives on events. The aim of this study was to investigate the effect of antenatal education based on the transformative learning theory on traumatic birth perception, fear of childbirth, and birth preparedness in pregnant women. The study was conducted as a randomized controlled trial with 54 participants. Data collection forms included a personal information form, the Traumatic Birth Perception Scale, the Prenatal Self-Assessment Scale, and the Wijma Birth Expectancy/Experience Scale. The Statistical Package for the Social Sciences 23.0 (Chicago, Illinois) version was used for data analysis. Histogram and Q-Q plots, and the Shapiro-Wilk test were used to assess the normality of the data distribution. Descriptive data regarding women's demographic characteristics were analyzed using frequencies, percentages, and mean values. Differences in demographic characteristics between groups were examined using the independent sample t-test, Mann-Whitney U test, and Chi-square test. Pre-test and post-test scores of the groups were analyzed using the independent sample t-test. A significance level of p<0.05 was accepted.

Study Overview

Study Type

Interventional

Enrollment (Actual)

54

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Kastamonu, Turkey, 37150
        • Kastamonu

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Be between the ages of 20-35
  • Be in the 30-32 weeks of gestation
  • Be a primigravida
  • Have at least basic literacy skills

Exclusion Criteria:

  • Have any chronic diseases
  • Have any psychiatric disorders
  • Be a high-risk pregnancy
  • Have any communication problems
  • Have communication issues

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Transformational Learning-Based Antenatal Education Group
This group will receive antenatal education based on transformational learning theory. The program aims to reduce birth fear and traumatic birth perception by providing participants with targeted information and strategies. Participants will gain knowledge and coping mechanisms to manage pain, stress, and anxiety during labor. The education will focus on raising awareness about the birth process, promoting psychological preparedness, and supporting post-birth recovery, all aimed at enhancing overall birth experience and well-being
The Transformational Learning-Based Antenatal Education Program helps pregnant women reduce birth-related anxiety and fear by utilizing transformational learning theory. Unlike traditional antenatal education, it emphasizes psychological preparedness, focusing on emotional well-being and coping strategies. The program includes interactive learning, group discussions, and self-reflection to engage participants actively. This approach aims to boost women's confidence and reduce stress as they approach labor and delivery.
No Intervention: Standard Antenatal Care Group
This group will receive standard antenatal care, which includes routine check-ups and general health education related to pregnancy. Participants will not receive the transformational learning-based antenatal education or any specific intervention related to birth fear or traumatic birth perception. The standard care focuses on general information about the physiological process of pregnancy and labor but does not address psychological preparedness or provide strategies for managing birth-related anxiety or fear.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perception of Traumatic Birth
Time Frame: Baseline: Week 30 of pregnancy (pre test); An average of 3 weeks (post test)
This will be assessed using the Traumatic Birth Perception Scale.The scale, developed by Yalnız et al. (2016), is called the Traumatic Birth Perception Scale. It is designed to assess the traumatic birth perception levels of women of reproductive age. It consists of 13 items that encompass the thoughts and emotions, such as anxiety, fear, and concern, that a woman experiences when thinking about childbirth. For each item, respondents rate their feelings on a scale from 0 ("no fear") to 10 ("extreme fear"). The total average score indicates the level of traumatic birth perception. The lowest and highest possible scores on the scale are 0 and 130, respectively. As the score increases, it reflects a higher perception of traumatic birth. The score ranges are as follows: 0-26 indicates very low, 27-52 low, 53-78 moderate, 79-104 high, and 105-130 indicates very high levels of traumatic birth perception. The Cronbach's alpha reliability coefficient of the scale is 0.89.
Baseline: Week 30 of pregnancy (pre test); An average of 3 weeks (post test)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Childbirth Readiness
Time Frame: Baseline: Week 30 of pregnancy (pre test); An average of 3 weeks (post test)
The Childbirth Readiness Subscale (PKDÖ-DHOÖ) was developed by Lederman in 1979 to assess women's adaptation to motherhood during the prenatal period. The scale, consisting of 79 items and using a 4-point Likert-type scale, was validated and tested for reliability in Turkey by Beydağ and Mete (2008). The scale includes 7 subscales: thoughts about the health of oneself and the baby, acceptance of pregnancy, acceptance of the maternal role, childbirth readiness, fear of childbirth, relationship with the mother, and relationship with the spouse. These subscales can be used independently. The general Cronbach's alpha for the Turkish version of the scale is 0.81, and the internal consistency reliability coefficients for the subgroups range from 0.72 to 0.85 (Beydağ & Mete, 2008). Scores on the scale range from 10 to 40. The Cronbach's alpha value for the Childbirth Readiness Subscale (DHOÖ) is 0.72. As the score increases, it indicates a lower level of readiness for childbirth.
Baseline: Week 30 of pregnancy (pre test); An average of 3 weeks (post test)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2024

Primary Completion (Actual)

December 12, 2024

Study Completion (Actual)

February 24, 2025

Study Registration Dates

First Submitted

March 21, 2025

First Submitted That Met QC Criteria

March 24, 2025

First Posted (Actual)

April 1, 2025

Study Record Updates

Last Update Posted (Actual)

April 1, 2025

Last Update Submitted That Met QC Criteria

March 24, 2025

Last Verified

June 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2023-KAEK-41

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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