Breastfeeding Stories and Video Education in Primiparous Mothers

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\

Inclusion Criteria: * 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 * Absence of any medical conditions hindering breastfeeding * Able to use a smartphone * Voluntary agreement to sign written informed consent * Having a healthy newborn * Presence of the sucking reflex in the infant * Absence of neonatal intensive care unit (NICU) admission requirement Exclusion Criteria: * 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