The Effect of Father-Sensitive Childbirth Education on Prenatal Paternal Attachment Level

April 23, 2025 updated by: Sevil Güner

This study was planned as a randomised controlled trial to examine the effects of a "Father-Sensitive Childbirth Preparation Class" on the level of prenatal attachment. The main question it aims to answer is:

1- How does a father-sensitive birth preparation class affect fathers' prenatal attachment levels?

It was conducted between February 1, 2024, and October 1, 2024, with expectant fathers living in Mersin province, whose spouses were experiencing their first pregnancy, who were between 20-32 weeks' gestation, and who were going to become fathers for the first time.

A total of 99 expectant fathers were included in the study - 50 in the intervention group and 49 in the control group. The intervention group was given a "Father-Sensitive Childbirth Preparation Training" consisting of four sessions, while the control group received a standard "Childbirth Preparation Training", also consisting of four sessions.

The "Descriptive Data Collection Tool" and the "Prenatal Father Attachment Scale" were used to collect the research data.

Study Overview

Study Type

Interventional

Enrollment (Actual)

99

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

    • Yenişehir
      • Mersin, Yenişehir, Turkey, 33000
        • Mersin University

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

Participants were:

  • Over 19 years of age,
  • At least literate,
  • Whose spouse was between 20 and 32 weeks pregnant,
  • Whose spouse was primigravida,
  • Whose spouse had a singleton pregnancy,
  • With no prior experience of pregnancy, childbirth, or parenting,
  • With no history of miscarriage, curettage, or perinatal loss,
  • Whose spouse had no pregnancy-related complications or risk factors,
  • Who had not previously attended any childbirth preparation training, pregnancy information classes, or parenting courses.

Exclusion Criteria:

Participants were excluded if they:

  • Had a spouse whose pregnancy was outside the 20-32 week gestation range,
  • Had a spouse with a multiple pregnancy,
  • Had any pregnancy-related complications or risk factors (high risk),
  • Had prior experience of pregnancy, birth, or parenting,
  • Had experienced miscarriage, curettage, or perinatal loss,
  • Had previously attended any childbirth preparation training, pregnancy information classes, or parenting courses.

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Father-Sensitive Birt Education
The father-sensitive birth education group was given "Father-Sensitive Childbirth Preparation Education" consisting of four sessions.
he father-sensitive education program preserves the basic structure of the Childbirth Preparation Education program, but has been enriched with original content that supports the active emotional and functional participation of fathers-to-be in the birth process.
Active Comparator: Standardized Birt Education
The control group received a total of 12 hours of standard childbirth preparation training, consisting of four three-hour sessions.
The control group received a total of 12 hours of standard childbirth preparation training, consisting of four three-hour sessions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Paternal Antenatal Attachment Scale (PAAS) total score mean
Time Frame: 14 days after completing the 12-hour father-sensitive childbirth preparation class

It consists of 16 questions in a 5-point Likert format, designed to evaluate the feelings and thoughts of expectant fathers towards the developing baby in the womb, based on their emotions, thoughts, and experiences over the past two weeks.

Nine items on the scale are reverse-scored, and the total score ranges from 16 to 80; higher scores indicate a stronger level of antenatal attachment.

14 days after completing the 12-hour father-sensitive childbirth preparation class

Collaborators and Investigators

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

Sponsor

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)

February 1, 2024

Primary Completion (Actual)

October 1, 2024

Study Completion (Actual)

October 14, 2024

Study Registration Dates

First Submitted

April 10, 2025

First Submitted That Met QC Criteria

April 23, 2025

First Posted (Actual)

May 1, 2025

Study Record Updates

Last Update Posted (Actual)

May 1, 2025

Last Update Submitted That Met QC Criteria

April 23, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • MERSINU*GHOSHANLİ*001

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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