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
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.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Beräknad)
Fas
- Inte tillämpbar
Kontakter och platser
Studiekontakt
- Namn: Berfin Aydın, BSc
- Telefonnummer: +90 539 894 91 77
- E-post: aydiinberfin@gmail.com
Studieorter
-
-
ümraniye
-
Istanbul, ümraniye, Turkiet (Türkiye)
- Koc University Hospital
-
Kontakt:
- Berfin Aydın, BSc
- Telefonnummer: +90 539 894 91 77
- E-post: aydiinberfin@gmail.com
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Beskrivning
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
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Hälsovårdsforskning
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Intervention group
Participants will receive routine hospital breastfeeding education along with audio recordings of successful breastfeeding stories and video-based 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.
|
|
Inget ingripande: control group
Participants will receive only routine hospital breastfeeding education.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Breastfeeding Self-Efficacy Scale Short Form (BSES-SF) Score
Tidsram: Baseline (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.
|
Baseline (within first 24 hours postpartum) and Postpartum 1st Month (Day 30)
|
|
LATCH Breastfeeding Assessment Tool Score
Tidsram: Baseline (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.
|
Baseline (within first 24 hours postpartum) and Discharge day (Day 2-3)
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
First-Month Evaluation Form
Tidsram: Postpartum 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.
|
Postpartum 1st Month (Day 30)
|
|
Education Satisfaction Form Score
Tidsram: Discharge day (Day 2-3)
|
Evaluates the participants' level of satisfaction with the educational materials provided.
Assessed using a structured questionnaire.
|
Discharge day (Day 2-3)
|
Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Beräknad)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 2026.332.IRB3.124
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