Breastfeeding Education

March 4, 2026 updated by: Elif DAĞLI, Cukurova University

The Effect of Breastfeeding Education Given to Primiparous Pregnant Women Using the Pecha Kucha Technique on Breastfeeding Self-efficacy and Maternal Attachment: a randomızed Controlled Experimental Study

This study was designed to determine the effect of breastfeeding education given to primiparous pregnant women using the pecha kucha technique on breastfeeding self-efficacy and maternal bonding. The research is a randomized controlled experimental study.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

The study population will consist of primiparous pregnant women in their third trimester who apply to the obstetrics and gynecology outpatient clinics of state hospitals. The sample will consist of primiparous pregnant women who volunteer to participate in the study. Data will be collected through face-to-face interviews. A personal information form, the "Maternal Attachment Scale," and the "Prenatal Breastfeeding Self-Efficacy Scale" will be used to collect data.

Study Type

Interventional

Enrollment (Estimated)

84

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 Contact

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:

  • Primiparous
  • 32 weeks or more of pregnancy
  • Being over 18 years old

Exclusion Criteria:

  • High-risk pregnancy
  • Multiparous

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: Pecha Kucha
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Behavioral: Pecha Kucha
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Other Names:
  • Control group
Active Comparator: control group
Participants in this group will receive breastfeeding education using the traditional PowerPoint presentation method.
Behavioral: Pecha Kucha
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Other Names:
  • Control group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maternal Attachment Inventory
Time Frame: up to 12 months
The Maternal Attachment Inventory (MAI) was developed by Mary E. Muller in 1994 to measure maternal attachment through love. Muller tested maternal adaptation and maternal attachment in two phases using Mercer's theory of maternal role adaptation. The Cronbach's alpha value of the MAI is 0.77 for mothers with one-month-old babies and 0.82 for mothers with four-month-old babies. The validity and reliability of the scale in Turkey were established by Kavlak and Şirin (2009). This study was methodologically planned to adapt the Maternal Attachment Inventory to the Turkish population and test its validity and reliability on mothers with one- and four-month-old babies. Each item is a 26-item scale with a 4-point Likert scale ranging from "always" to "never". Each item includes direct statements and is scored as follows: always (a)=4 points, frequently (b)=3 points, sometimes (c)=2 points, and never (d)=1 point. The lowest possible score on the scale measuring maternal feelings and behavior
up to 12 months

Collaborators and Investigators

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

Sponsor

Cukurova University

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 (Estimated)

March 10, 2026

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

October 1, 2026

Study Registration Dates

First Submitted

February 19, 2026

First Submitted That Met QC Criteria

March 4, 2026

First Posted (Actual)

March 9, 2026

Study Record Updates

Last Update Posted (Actual)

March 9, 2026

Last Update Submitted That Met QC Criteria

March 4, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Balcalı

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

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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