Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

The Effect of Podcast Breastfeeding Training on Mothers of Preterm Infants

16 giugno 2026 aggiornato da: Dilek Kucuk Alemdar

The Effect of Podcast Breastfeeding Training on Breastfeeding Outcomes of Mothers of Preterm Infants Hospitalized in the Neonatal Intensive Care Unit (NICU): A Randomized Controlled Study

The aim of this study is to examine the effect of breastfeeding education provided via podcast to mothers of preterm infants admitted to the neonatal intensive care unit on the mothers' breastfeeding success, awareness, motivation, self-efficacy, and perception of insufficient milk supply. The research aims to help mothers overcome challenges in the breastfeeding process by increasing their knowledge levels and to strengthen their confidence in this process. Thus, the goal is to better meet the nutritional needs of preterm infants and to improve mothers' breastfeeding experiences in a positive direction.

Panoramica dello studio

Stato

Reclutamento

Descrizione dettagliata

The aim of this study is to examine the effect of breastfeeding education provided via podcast to mothers of preterm infants admitted to the neonatal intensive care unit on the mothers' breastfeeding success, awareness, motivation, self-efficacy, and perception of insufficient milk supply. The sample for this study, conducted using a pre-test-post-test randomized controlled experimental design, consisted of patients admitted to the Neonatal Intensive Care Unit at Ordu University Education and Research Hospital at the Neonatal Intensive Care Unit of Ordu University Education and Research Hospital, who were informed about the purpose of the current study, provided written and verbal consent to participate in the study, and were preterm infants between 34 and 37 weeks of gestation, along with their mothers who met the inclusion criteria. The "Demographic/Obstetric and Neonatal Characteristics Form," "Breastfeeding Motivation Scale," "Breastfeeding Awareness Scale," "Breastfeeding Self-Efficacy Scale," and "Perceived Insufficient Milk Scale" were used to collect data. The sample will consist of mothers of preterm infants between 34 and 37 weeks of gestation who meet the inclusion criteria. The sample size for the study was determined to be 26 mothers, calculated using G-Power analysis with a 95% confidence level (1-α), 80% power (1-β), an effect size of 0.80, and an independent samples t-test. Due to the possibility of data loss, the number of participants was increased based on the results of the power analysis, and it was planned to include 56 mothers who met the selection criteria in the study sample. A podcast series on breastfeeding education will be shared with the mothers in the experimental group via a digital platform (WhatsApp). The content will cover: breastfeeding preterm infants, why breast milk is important, the composition of breast milk and its importance for preterm infants, and the benefits of breast milk for preterm infants, the breastfeeding process at YYBÜ, conditions for expressing and storing milk, challenges encountered during breastfeeding and their solutions, ways to increase milk production, seeking support for breastfeeding at YYBÜ, the role of breast milk in the nutrition of preterm infants, and recommendations for breastfeeding. Daily follow-up calls will be used to track whether the mothers listened to the podcasts. Mothers in the control group received only the standard breastfeeding education provided under the hospital protocol. No podcasts or other additional support were provided. The scales administered after the education provided via the podcast and standard care were reapplied to mothers in both groups. This will allow for a comparative evaluation of changes between the experimental and control groups.

Tipo di studio

Interventistico

Iscrizione (Stimato)

56

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • The mother must volunteer to participate in the study,
  • The mother must be 18 years of age or older
  • After being accepted into the study, the mother must express her intention to breastfeed her baby
  • The mother must be able to speak and read Turkish
  • The mother's baby being between 32 and 37 weeks gestation

Exclusion Criteria:

  • Illegal drug and tobacco use by the mother
  • The mother's use of alcohol during pregnancy and after childbirth
  • Active tuberculosis in the mother
  • The presence of Herpes simplex virus lesions on the mother's breast
  • The presence of a maternal psychiatric disorder
  • Having prior experience breastfeeding a preterm infant
  • Having a condition that prevents breastfeeding
  • Mothers who have had multiple births.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Terapia di supporto
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Triplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Podcast group
A podcast series on breastfeeding education will be shared with the mothers in the experimental group via a digital platform (WhatsApp). The content will cover: breastfeeding preterm infants, why breast milk is important, the composition of breast milk and its importance for preterm infants, and the benefits of breast milk for preterm infants, the breastfeeding process at YYBÜ, conditions for expressing and storing milk, challenges encountered during breastfeeding and their solutions, ways to increase milk production, seeking support for breastfeeding at YYBÜ, the role of breast milk in the nutrition of preterm infants, and recommendations for breastfeeding. Daily follow-up calls will be conducted to monitor whether the mothers are listening to the podcasts.
A podcast series on breastfeeding education will be shared with the mothers in the experimental group via a digital platform (WhatsApp). The content will cover: breastfeeding preterm infants, why breast milk is important, the composition of breast milk and its importance for preterm infants, and the benefits of breast milk for preterm infants, the breastfeeding process at YYBÜ, conditions for expressing and storing milk, challenges encountered during breastfeeding and their solutions, ways to increase milk production, seeking support for breastfeeding at YYBÜ, the role of breast milk in the nutrition of preterm infants, and recommendations for breastfeeding. Daily follow-up calls will be conducted to monitor whether the mothers are listening to the podcasts.
Nessun intervento: Control group
Mothers in the control group will receive only the standard breastfeeding education provided as part of the hospital protocol.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Breastfeeding Awareness Scale
Lasso di tempo: One day after admission to the hospital. One day before discharge from the hospital.
This is a 9-item measurement tool designed to assess awareness-based breastfeeding practices during the postpartum period. The scale is unidimensional and was developed using a 5-point Likert scale. Responses to the scale items range from (1) Never to (5) Always. The total score on the scale ranges from 9 to 45, and as the total score increases, the level of awareness regarding breastfeeding also increases.
One day after admission to the hospital. One day before discharge from the hospital.
Breastfeeding Motivation Scale (BMS)
Lasso di tempo: One day after admission to the hospital. One day before discharge from the hospital.
The scale consists of 24 items and has 5 subscales. There is no total score for the scale. Subscale scores are calculated by taking the average of the subscale item scores. As the score on a subscale increases, the motivation associated with that subscale also increases. For multiparous mothers, the scale consists of 24 items and six factors, while for primiparous mothers, it consists of 23 items and five subfactors. The 24-item scale can be used for both multiparous and primiparous mothers.
One day after admission to the hospital. One day before discharge from the hospital.
Breastfeeding Self-Efficacy Scale (Short Form)
Lasso di tempo: One day after admission to the hospital. One day before discharge from the hospital.
The Breastfeeding Self-Efficacy Short Form Scale is a 5-point Likert-type scale, with responses rated as follows: 1 = "Not at all confident," 2 = "Not very confident," 3 = "Sometimes confident," 4 = "Confident," and 5 = "Very confident." The minimum score on the scale is 14, and the maximum is 70. A higher score indicates higher breastfeeding self-efficacy. The short form of the scale is easy to administer and accurately assesses self-efficacy.
One day after admission to the hospital. One day before discharge from the hospital.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Inadequate Breastfeeding Perception Scale
Lasso di tempo: One day after admission to the hospital. One day before discharge from the hospital.

It is a measure used to assess breastfeeding mothers' perceptions of insufficient milk supply.

The first question asks the mother about her belief regarding whether she is feeding her baby sufficiently. The mother answers this question with "yes" or "no." The other questions on the scale are designed to measure the perception of milk insufficiency. Mothers are asked to rate these questions on a scale of 0 to 10. A score of "0" indicates that the milk is perceived as completely insufficient, while a score of "10" indicates that the milk is perceived as completely sufficient. A minimum score of 0 and a maximum score of 50 can be obtained on the scale. A higher total score indicates an increased perception of milk sufficiency.

One day after admission to the hospital. One day before discharge from the hospital.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

20 luglio 2025

Completamento primario (Stimato)

15 giugno 2026

Completamento dello studio (Stimato)

30 giugno 2026

Date di iscrizione allo studio

Primo inviato

8 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

16 giugno 2026

Primo Inserito (Effettivo)

22 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

22 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

16 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • BAEK250

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

Because it contains personal data.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Sottoscrivi