Breastfeeding Stories and Video Education in Primiparous Mothers
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorYeditepe University
About this trial
The Effect of Successful Breastfeeding Stories and Video-Based Education on Breastfeeding Self-Efficacy and Breastfeeding Success in Primiparous Mothers: A Randomized Controlled Trial
Objective: This study was planned to determine the effect of the combined use of audio recordings based on successful breastfeeding stories and video-based breastfeeding education on breastfeeding self-efficacy and breastfeeding success among primiparous mothers.
Methods: This study will be conducted using a randomized controlled experimental design. The population of the study will consist of primiparous mothers who give birth at the Obstetrics and Gynecology Clinic of Koç University Hospital between September 2026 and February 2027. The sample will consist of a total of 70 primiparous mothers (35 intervention and 35 control) who meet the inclusion criteria and are assigned to the intervention and control groups using a computer-assisted simple randomization method. In addition to routine breastfeeding education provided at the hospital, mothers in the intervention group will receive audio recordings based on successful breastfeeding stories and video-based breastfeeding education. The control group will receive only the routine breastfeeding education provided at the hospital. Data will be collected using the Descriptive Characteristics Form, Postpartum Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF), LATCH Breastfeeding Assessment Tool, Educational Materials Satisfaction Form, and First-Month Evaluation Form. Data will be analyzed using SPSS version 25.0. Descriptive statistics, independent-samples t-test, paired-samples t-test, chi-square test, and repeated-measures analysis of variance (ANOVA) will be used. The statistical significance level will be accepted as p\<0.05.
Expected Results: It is anticipated that the audio recordings based on successful breastfeeding stories and the video-based education program will increase breastfeeding self-efficacy and breastfeeding success among primiparous mothers.
Conclusion: The findings obtained from this study are expected to contribute to the planning of evidence-based nursing interventions aimed at improving breastfeeding self-efficacy and breastfeeding success among primiparous mothers, provide a scientific basis for innovative educational models that can be used to support breastfeeding, and guide the development of standardized breastfeeding education programs that can be implemented in postpartum care services.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Being 18 years of age or older
Able to read and write in Turkish
Being primiparous
Having given birth to a singleton live birth at >37 weeks of gestation
Disqualifiers
Withdrawal of consent / wishing to leave the study
Incomplete completion of data collection tools
Infant experiencing severe health issues requiring hospital readmission
Loss of contact during the follow-up period
Trial design
Design model
Parallel
Treatments tested in this trial
Routine Breastfeeding Education with Audio Stories and Video Education
BehavioralIn addition to the routine breastfeeding education provided by the hospital, participants in this group receive audio recordings based on successful breastfeeding stories and video-based breastfeeding education.
Treatment groups
70 Participants
are divided into 2 treatment groupsGroup A: Intervention groupExperimental treatment 1 intervention
Group B: control groupNo intervention 0 interventions
Trial outcomes
Primary outcomes
1
Breastfeeding Self-Efficacy Scale Short Form (BSES-SF) Score
Assessed using the Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF). Total scores range from 14 to 70, with higher scores indicating higher levels of breastfeeding self-efficacy.
Time frame
Baseline (within first 24 hours postpartum) and Postpartum 1st Month (Day 30)2
LATCH Breastfeeding Assessment Tool Score
Evaluates breastfeeding performance across 5 parameters (Latch, Audible swallowing, Type of nipple, Comfort, Hold). Total scores range from 0 to 10, with higher scores indicating higher breastfeeding success.
Time frame
Baseline (within first 24 hours postpartum) and Discharge day (Day 2-3)Secondary outcomes
1
First-Month Evaluation Form
Administered by the researcher via phone or online communication methods at the 1st month postpartum. The researcher reads the questions to the participant without guidance and records the responses to evaluate breastfeeding status and outcomes.
Time frame
Postpartum 1st Month (Day 30)2
Education Satisfaction Form Score
Evaluates the participants' level of satisfaction with the educational materials provided. Assessed using a structured questionnaire.
Time frame
Discharge day (Day 2-3)Sponsors and contacts
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Source ClinicalTrials.gov
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