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Набор по приглашению NCT07543133

Simulation-Based Childbirth Training and Midwives' Outcomes

Без фазы С лечением Education Maternal Health

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Simulation-Based Childbirth Management Training.
Кому может быть актуально
Состояния в реестре: Education, Maternal Health. Базовые параметры: 18 лет — 45 лет · Женщины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Turkey (Türkiye)
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

The Effect of Simulation-Based Childbirth Management Training on Safe Motherhood Practices and Intrinsic Motivation Among Midwives: A Randomized Controlled Study

Обзор

This randomized controlled study aims to evaluate the effect of simulation-based childbirth management training on safe motherhood practices and intrinsic motivation among midwives. Participants will be randomly assigned to either an intervention group receiving simulation-based training or a control group receiving no additional training. Outcomes will be assessed using validated scales before and after the intervention.

Подробное описание

Simulation-based training is an effective educational approach that allows healthcare professionals to develop clinical skills in a safe and controlled environment. This study aims to evaluate the effectiveness of simulation-based childbirth management training on safe motherhood practices and intrinsic motivation among midwives.

The study is designed as a randomized controlled trial with a pre-test and post-test design. A total of 132 midwives will be included and randomly assigned to intervention and control groups. The intervention group will receive a structured simulation-based training program over five days, including obstetric scenarios such as normal delivery, postpartum hemorrhage, shoulder dystocia, and other obstetric emergencies. Each session will include pre-briefing, simulation practice, and debriefing.

The control group will continue routine practices without any additional intervention. Data will be collected using a Personal Information Form, Safe Motherhood Scale (for healthcare professionals), and Intrinsic Motivation Scale. Outcomes will be measured before and after the intervention.

The study aims to contribute to evidence-based midwifery education by evaluating both clinical practice outcomes and motivational factors.

Вмешательства

  • Поведенческое Simulation-Based Childbirth Management Training
    Participants will receive simulation-based childbirth management training for five consecutive days (8 hours per day), including structured obstetric scenarios and debriefing sessions.

Первичные конечные точки

  • Safe Motherhood Practices Level [Срок оценки: Before training and immediately after training (Day 5)]
  • Intrinsic Motivation Level [Срок оценки: Before training and immediately after training (Day 5)]

Критерии участия

Критерии включения

  • Midwives working in healthcare institutions affiliated with the provincial health directorate
  • Having 5 years or less professional experience
  • Actively involved in prenatal, intrapartum, or postpartum care
  • Voluntary participation with written informed consent

Критерии исключения

  • Working in administrative positions
  • Previously received simulation-based childbirth or advanced obstetric simulation training
  • Inability to attend the full training program or complete data collection

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Поддерживающая терапия

Центры проведения

Turkey (Türkiye) · 1 центр
  • Selçuk University — Konya

Идентификаторы

NCT: NCT07543133 · 328886655 · 11122554533

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗