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Effectiveness of Breastfeeding Education Using a Lactation Simulation Model Among Nursing Students: A Randomized Controlled Trial (LSM-BE)

18 lipca 2026 zaktualizowane przez: SINEM CATAKOGLU, Izmir Katip Celebi University

The Effectiveness of Breastfeeding Education Using a Lactation Simulation Model on Nursing Students' Breastfeeding Education Skills, Mothers' Breastfeeding Self-Efficacy, Breastfeeding Success, and Student Satisfaction: A Randomized Controlled Trial

Breastfeeding education provided by nurses is an important determinant of breastfeeding success and maternal breastfeeding self-efficacy. Nursing students should acquire effective breastfeeding counseling skills before entering clinical practice. Simulation-based education offers students the opportunity to develop communication and clinical skills in a safe learning environment.

The aim of this randomized controlled trial was to evaluate the effectiveness of breastfeeding education using a lactation simulation model among fourth-year nursing students. Students were randomly assigned to either an intervention group receiving simulation-based breastfeeding education using a lactation simulation model or a control group receiving routine theoretical breastfeeding education. During their maternity clinical placement, students provided standardized breastfeeding education to postpartum mothers.

The primary outcomes were students' breastfeeding education skills and maternal breastfeeding self-efficacy. Secondary outcomes included breastfeeding success assessed by the LATCH Breastfeeding Assessment Tool and students' educational satisfaction. The findings of this study are expected to provide evidence supporting the integration of simulation-based breastfeeding education into undergraduate nursing curricula.

Przegląd badań

Szczegółowy opis

Breastfeeding is recognized as the optimal method of infant feeding and is associated with significant short- and long-term health benefits for both mothers and infants. International organizations recommend exclusive breastfeeding during the first six months of life and continued breastfeeding with appropriate complementary feeding thereafter. Effective breastfeeding counseling provided by healthcare professionals is essential for improving breastfeeding outcomes.

Nursing students frequently encounter breastfeeding mothers during maternity clinical placements; however, many students report insufficient confidence and practical competence in breastfeeding counseling. Simulation-based education has emerged as an effective educational strategy that enables students to practice clinical procedures, communication skills, and patient education in a realistic but safe learning environment before interacting with actual patients.

This randomized controlled trial evaluated the effectiveness of a lactation simulation model on nursing students' breastfeeding education competencies and maternal breastfeeding outcomes. Fourth-year nursing students enrolled in the Department of Nursing at Izmir Katip Celebi University were randomly allocated to intervention and control groups using a computer-generated randomization sequence.

All participants received routine theoretical breastfeeding education as part of the undergraduate nursing curriculum. Students allocated to the intervention group additionally received simulation-based breastfeeding education using a lactation simulation model in the Women's Health Nursing Skills Laboratory before beginning their maternity clinical placement. The simulation sessions focused on breastfeeding techniques, positioning, latch assessment, management of common breastfeeding problems, effective communication, and breastfeeding counseling.

Following completion of the educational intervention, students provided standardized breastfeeding education to postpartum mothers hospitalized in the postpartum unit of Izmir Ataturk Training and Research Hospital. Maternal breastfeeding self-efficacy was evaluated using the Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF), breastfeeding success was assessed using the LATCH Breastfeeding Assessment Tool, students' educational performance was evaluated using a Breastfeeding Education Evaluation Form, and educational satisfaction was assessed using the Adult Education Satisfaction Scale.

The study aimed to determine whether simulation-based breastfeeding education improved nursing students' educational competencies and contributed to better maternal breastfeeding outcomes compared with routine theoretical education alone.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

60

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

      • Izmir, Turcja (Türkiye)
        • İzmir Atatürk Training and Research Hospital

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Tak

Opis

Inclusion Criteria:

-

Nursing Students:

  • Fourth-year undergraduate nursing students enrolled in the Department of Nursing at Izmir Katip Celebi University.
  • Students undertaking their maternity nursing clinical placement during the study period.
  • Students who voluntarily agreed to participate and provided written informed consent.

Postpartum Mothers:

  • Mothers hospitalized in the postpartum unit of Izmir Ataturk Training and Research Hospital.
  • Mothers aged 18 years or older.
  • Mothers who delivered a healthy singleton infant.
  • Mothers who were breastfeeding their infants.
  • Mothers who were able to communicate in Turkish.
  • Mothers who voluntarily agreed to participate and provided written informed consent.

Exclusion Criteria:

-

Nursing Students:

  • Students who did not complete the educational intervention or clinical placement.
  • Students who withdrew from the study or had excessive absenteeism during the clinical placement.

Postpartum Mothers:

  • Mothers with medical conditions contraindicating breastfeeding.
  • Infants with congenital anomalies or medical conditions preventing breastfeeding.
  • Mothers whose infants required admission to the neonatal intensive care unit.
  • Mothers who declined participation or withdrew consent.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Inny
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Intervention Group
Nursing students assigned to the intervention group will receive breastfeeding education supported by a lactation model in addition to the standard breastfeeding course content. The training will include theoretical information and practical skills training using a lactation simulation model before clinical practice. Students will provide breastfeeding education to postpartum mothers during their clinical placement.
The intervention consists of breastfeeding education provided to nursing students using a lactation simulation model. The training includes theoretical information and practical skills training before clinical practice. Students will practice breastfeeding support skills using the lactation model and subsequently provide breastfeeding education to postpartum mothers.
Brak interwencji: Control Group
Nursing students assigned to the control group will receive standard breastfeeding education provided within the undergraduate nursing curriculum. Students will not receive additional training with a lactation model before clinical practice. They will provide breastfeeding education to postpartum mothers during their clinical placement according to the standard curriculum.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Breastfeeding Education Skills of Nursing Students
Ramy czasowe: During the maternity clinical placement (up to 4 weeks after the educational intervention)
Nursing students' breastfeeding education skills assessed using the Breastfeeding Education Evaluation Form after completion of the educational intervention and during clinical practice.
During the maternity clinical placement (up to 4 weeks after the educational intervention)
Maternal Breastfeeding Self-Efficacy
Ramy czasowe: Before hospital discharge (within 48-72 hours postpartum)
Maternal breastfeeding self-efficacy assessed using the Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF) after receiving breastfeeding education from nursing students.
Before hospital discharge (within 48-72 hours postpartum)

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Breastfeeding Success
Ramy czasowe: Before hospital discharge (within 48-72 hours postpartum)
Breastfeeding success assessed using the LATCH Breastfeeding Assessment Tool.
Before hospital discharge (within 48-72 hours postpartum)
Student Educational Satisfaction
Ramy czasowe: Immediately after completion of the educational intervention
Students' satisfaction with the simulation-based educational program assessed using the Adult Education Satisfaction Scale.
Immediately after completion of the educational intervention

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

1 kwietnia 2025

Zakończenie podstawowe (Rzeczywisty)

30 marca 2026

Ukończenie studiów (Rzeczywisty)

30 czerwca 2026

Daty rejestracji na studia

Pierwszy przesłany

18 lipca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

18 lipca 2026

Pierwszy wysłany (Rzeczywisty)

22 lipca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

22 lipca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

18 lipca 2026

Ostatnia weryfikacja

1 lipca 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

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