- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07657819
DİGİTAL STORYTELLİNG AND BREASTFEEDİNG EDUCATİON
EVALUATION OF THE EFFECT OF BREASTFEEDING EDUCATION DELIVERED USING DIGITAL STORYTELLING METHODS ON MOTHERS' BREASTFEEDING SUCCESS AND BREASTFEEDING SELF-EFFICACY
Study Overview
Status
Detailed Description
Breastfeeding is one of the most important factors affecting maternal and infant health. Educational interventions may improve breastfeeding outcomes by increasing mothers' confidence and knowledge regarding breastfeeding practices. Digital storytelling is an innovative educational approach that combines visual, audio, and narrative elements to improve learning experiences.
This study was conducted to evaluate the effectiveness of digital storytelling-based breastfeeding education on breastfeeding self-efficacy and breastfeeding success among postpartum women. The study was carried out between September 2024 and December 2025 in the postpartum unit of Etlik City Hospital. Participants were assigned to either an intervention group receiving digital storytelling-based breastfeeding education or a control group receiving standard breastfeeding education.
Data were collected using a Demographic Information Form, the Breastfeeding Self-Efficacy Scale-Short Form, and the Bristol Breastfeeding Assessment Tool. The findings of the study are expected to contribute to the development of innovative breastfeeding education strategies and support evidence-based maternal health practices.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Ankara, Turkey (Türkiye), 06010
- Etlik City Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Women aged 18 years and older
- Postpartum women
- Able to communicate in Turkish
- Literate
- Healthy mother and healthy newborn
- Voluntarily agreed to participate in the study
Exclusion Criteria:
- Refusal to participate in the study
- Mothers with conditions preventing breastfeeding
- Mothers with severe maternal or neonatal complications
- Communication problems preventing participation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Experimental Group
Participants received breastfeeding education prepared using the digital storytelling method.
Breastfeeding self-efficacy and breastfeeding success were evaluated after the intervention.
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Control Group
Participants received routine breastfeeding education provided by the hospital.
Breastfeeding self-efficacy and breastfeeding success were evaluated after the intervention.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Breastfeeding Self-Efficacy
Time Frame: Within 24 hours after breastfeeding education
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Measured using the Breastfeeding Self-Efficacy Scale-Short Form.
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Within 24 hours after breastfeeding education
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Breastfeeding Success
Time Frame: 5 and 12 hours after breastfeeding education
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Measured using the Bristol Breastfeeding Assessment Tool.
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5 and 12 hours after breastfeeding education
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ZC-DSB-2024-01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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