Fathers' Breastfeeding Self-efficiency

March 18, 2024 updated by: Elif DAĞLI, Cukurova University

Examining the Effect of Digital Storying on Fathers' Breastfeeding Self-efficiency

The purpose of this study was planned to examine the effect of the education given through digital storytelling method on fathers' breastfeeding self-efficacy perception. The research is in a quasi-experimental design with no pretest-posttest control group.

Study Overview

Status

Completed

Conditions

Detailed Description

In the study, intervention and control group data will be collected using the Personal Information Collection Form and the Father Breastfeeding Self-Efficacy Scale.

Personal Information Form: The Personal Information Form was developed by the researchers in line with literature information. There are questions about the socio-demographic characteristics of fathers, the role and responsibilities of fathers during breastfeeding.

Breastfeeding Self-Efficacy Scale for Fathers Short Form: The Breastfeeding Self-Efficacy Scale for Fathers was created by Dennis et al. to measure fathers' self-efficacy in supporting their spouses in breastfeeding, and its Cronbach's alpha value is 0.92.

Study Type

Interventional

Enrollment (Actual)

80

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

      • Adana, Turkey, 01330
        • Çukurova University
    • Balcalı
      • Adana, Balcalı, Turkey, 01 330
        • Çukurova University
      • Adana, Balcalı, Turkey, 01330
        • Çukurova

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:

  • Not being between 0-6 weeks postpartum, not being married, not being literate

Exclusion Criteria:

-

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: Storytelling Intervention
The Storytelling video intervention created is approximately 20 minutes long.
A storytelling fertility awareness video intervention, approximately 10 minutes in length, guided by a situation-specific theoretical framework and storytelling/narrative communication theory, was developed by the researchers.
Other Names:
  • control group
Active Comparator: control group
Routine hospital protocol was applied to the women in this group. Storytelling fertility awareness video intervention was also given to the control group after the study.
A storytelling fertility awareness video intervention, approximately 10 minutes in length, guided by a situation-specific theoretical framework and storytelling/narrative communication theory, was developed by the researchers.
Other Names:
  • control group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Breastfeeding Self-Efficacy Scale for Fathers Short Form
Time Frame: up to 12 months
Paternal Breastfeeding Self-Efficacy Scale- Short Form (Paternal BSES-SF): Paternal BSES-SF was developed by Dennis et al. (2018) to measure paternal self-efficacy in supporting their wives in breastfeeding and Cronbach's alpha value was 0.92. A Turkish validity-reliability study was conducted by Küçükoğlu (2022) and Cronbach's alpha value was found to be 0.93. The scale was applied to all fathers with newborn and breastfed infants and consisted of a single dimension with 14 items evaluated on a 5-point Likert scale (1=never 2=sometimes 3=sometimes 4=often 5=always). There are no reverse scored items in the scale. The minimum score to be obtained from the scale is 14 and the maximum score is 70. The cut-off point of the scale has not been determined,higher scores indicate higher confidence.
up to 12 months

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)

February 1, 2023

Primary Completion (Actual)

May 30, 2023

Study Completion (Actual)

July 30, 2023

Study Registration Dates

First Submitted

December 15, 2023

First Submitted That Met QC Criteria

March 18, 2024

First Posted (Actual)

March 20, 2024

Study Record Updates

Last Update Posted (Actual)

March 20, 2024

Last Update Submitted That Met QC Criteria

March 18, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • self-efficiency

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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