NCT06320275

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

3 active sites

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

Study Start

First participant enrolled

February 1, 2023

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2023

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2023

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

December 15, 2023

Completed
3 months until next milestone

First Posted

Study publicly available on registry

March 20, 2024

Completed
Last Updated

March 20, 2024

Status Verified

March 1, 2024

Enrollment Period

4 months

First QC Date

December 15, 2023

Last Update Submit

March 18, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Breastfeeding Self-Efficacy Scale for Fathers Short Form

    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

Study Arms (2)

Storytelling Intervention

EXPERIMENTAL

The Storytelling video intervention created is approximately 20 minutes long.

Behavioral: Storytelling Intervention

control group

ACTIVE COMPARATOR

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.

Behavioral: Storytelling Intervention

Interventions

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.

Also known as: control group
Storytelling Interventioncontrol group

Eligibility Criteria

Age18 Years+
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

Cukurova University

Adana, Balcalı, 01 330, Turkey (Türkiye)

Location

Çukurova

Adana, Balcalı, 01330, Turkey (Türkiye)

Location

Çukurova University

Adana, 01330, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Breast Feeding

Interventions

Control Groups

Condition Hierarchy (Ancestors)

Feeding BehaviorBehavior

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

December 15, 2023

First Posted

March 20, 2024

Study Start

February 1, 2023

Primary Completion

May 30, 2023

Study Completion

July 30, 2023

Last Updated

March 20, 2024

Record last verified: 2024-03

Data Sharing

IPD Sharing
Will not share

Locations