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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

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07784439
Enrollment
70
Registered
2026-08-25
Start date
2026-09-01
Completion date
2027-06-01
Last updated
2026-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breastfeeding, Breastfeeding Self-Efficacy

Keywords

Primiparous mother, video-based education, successful breastfeeding story, randomized controlled trial, LATCH, BSES-SF

Brief summary

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.

Interventions

BEHAVIORALRoutine Breastfeeding Education with Audio Stories and Video Education

In 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.

Sponsors

Yeditepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Breastfeeding Self-Efficacy Scale Short Form (BSES-SF) ScoreBaseline (within first 24 hours postpartum) and Postpartum 1st Month (Day 30)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.
LATCH Breastfeeding Assessment Tool ScoreBaseline (within first 24 hours postpartum) and Discharge day (Day 2-3)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.

Secondary

MeasureTime frameDescription
First-Month Evaluation FormPostpartum 1st Month (Day 30)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.
Education Satisfaction Form ScoreDischarge day (Day 2-3)Evaluates the participants' level of satisfaction with the educational materials provided. Assessed using a structured questionnaire.

Countries

Turkey (Türkiye)

Contacts

CONTACTBerfin Aydın, BSc
aydiinberfin@gmail.com+90 539 894 91 77

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 26, 2026