Effect of Postpartum Hemorrhage Management Education Given With Kahoot Method on Knowledge, Self-Confidence in Intervention and Motivation Levels of Midwifery Students

Обзор

This study was planned to investigate the effect of postpartum hemorrhage management training given with the Kahoot method on the knowledge, self-confidence in intervention and motivation levels of midwifery students. The research population will consist of third-year students studying at the Department of Midwifery, Hamidiye Faculty of Health Sciences (HSBF), Health Sciences University (SBU) in the spring semester of the 2024-2025 academic year (N: 80). In this semi-experimental pre-test and post-test design and control group planned study, in order to determine the sample size; the data were normally distributed, the standard deviation of the main mass was estimated as 1 and the effect size (effect size, difference) was estimated as 0.8. For the analysis to be conducted, it was calculated that the highest power value of the study would be 0.942182 if two independent n₁=40, n₂=40 samples were taken at a significance level of 5%. In addition, the adequacy of the sample size in the study will be evaluated with post hoc power analysis after the data are collected. Students who volunteer to participate in the study will be assigned to the intervention and control groups using the computer-aided simple random sampling method. Computer-aided randomization will be used in the study, and the number of cases will be entered through the program with the URL address https://www.randomizer.org and random assignment will be made to the intervention and control groups. Before the data collection forms begin training, the "Informed Voluntary Consent Form" will be shared with the students participating in the study and their approval will be requested. The "Introductory Information Form", "Postpartum Hemorrhage Management Information Form", "Self-Confidence/Competence Scale in Patient Intervention" and "Motivation Scale Regarding the Teaching Material" will be applied to the students who agree to participate in the study.

Вмешательства

• Другое Games-based education
  A 5-question trial test on Kahoot usage will be applied to the students in the intervention group (questions must be prepared in advance, students must have full internet connection, students must enter the Kahoot application with their phones, students must enter the code required to enter the platform, etc.). The questions that make up the trial test will be created independently of the subject covered in the theoretical training and students will be adapted to Kahoot. After the 2-hour theoret

Первичные конечные точки

• Introductory Information Form [Срок оценки: 10 minutes]
• Postpartum Hemorrhage Management Information Form [Срок оценки: 10 minutes]
• Self-Confidence/Competence in Patient Intervention Scale [Срок оценки: 10 minutes]
• Motivation Scale Related to Instructional Material [Срок оценки: 10 minutes]

Вторичные конечные точки (4)

• Introductory Information Form [Срок оценки: 10 minutes]
• Postpartum Hemorrhage Management Information Form [Срок оценки: 10 minutes]
• Self-Confidence/Competence in Patient Intervention Scale [Срок оценки: 10 minutes]
• Motivation Scale Related to Instructional Material [Срок оценки: 10 minutes]

Критерии участия

Критерии включения

• Volunteering to participate in the research.
• Having internet access,
• Having a smart phone,
• Being an active student in the 3rd year of the Department of Midwifery at Hamidiye Health Sciences Faculty, University of Health Sciences.

Критерии исключения

• Being a passive student in the 3rd year of the Midwifery Department of Hamidiye Health Sciences Faculty, University of Health Sciences.
• Not meeting the inclusion criteria.

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

Простое слепое

Основная цель

Другое

Центры проведения

Turkey (Türkiye) · 1 центр

• University of Health Sciences — Istanbul

Идентификаторы

NCT: NCT06897371 · SBU-AYDINKARTAL-013

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗