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.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Tipo de estudo
Inscrição (Estimado)
Estágio
- Não aplicável
Contactos e Locais
Contato de estudo
- Nome: Berfin Aydın, BSc
- Número de telefone: +90 539 894 91 77
- E-mail: aydiinberfin@gmail.com
Locais de estudo
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ümraniye
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Istanbul, ümraniye, Turquia (Türkiye)
- Koc University Hospital
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Contato:
- Berfin Aydın, BSc
- Número de telefone: +90 539 894 91 77
- E-mail: aydiinberfin@gmail.com
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Pesquisa de serviços de saúde
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: Intervention group
Participants will receive routine hospital breastfeeding education along with audio recordings of successful breastfeeding stories and video-based education.
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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.
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Sem intervenção: control group
Participants will receive only routine hospital breastfeeding education.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Breastfeeding Self-Efficacy Scale Short Form (BSES-SF) Score
Prazo: Baseline (within first 24 hours postpartum) and Postpartum 1st Month (Day 30)
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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.
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Baseline (within first 24 hours postpartum) and Postpartum 1st Month (Day 30)
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LATCH Breastfeeding Assessment Tool Score
Prazo: Baseline (within first 24 hours postpartum) and Discharge day (Day 2-3)
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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.
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Baseline (within first 24 hours postpartum) and Discharge day (Day 2-3)
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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First-Month Evaluation Form
Prazo: Postpartum 1st Month (Day 30)
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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.
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Postpartum 1st Month (Day 30)
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Education Satisfaction Form Score
Prazo: Discharge day (Day 2-3)
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Evaluates the participants' level of satisfaction with the educational materials provided.
Assessed using a structured questionnaire.
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Discharge day (Day 2-3)
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Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 2026.332.IRB3.124
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
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