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Teaching Method With Simulation in Gestational Diabetes Mellitus Management

2022年4月23日 更新者:Esra Yılmaz、Saglik Bilimleri Universitesi

Evaluation of the Effectiveness of Teaching Method With Simulation in Gestational Diabetes Mellitus Management

Gestational Diabetes Mellitus is one of the common risk factors of pregnancy and occurs for the first time during pregnancy. It adversely affects maternal and fetal health and causes an increase in morbidity and mortality rates. In this context, it is very important to identify possible risks for GDM, plan, implement and evaluate initiatives, provide emergency crisis management in a short time without damage, and increase the self-confidence of midwives. In recent years, interest in simulation methods and skill acquisition training in midwifery education has increased. Research; In the management of GDM, to increase the satisfaction and self-confidence level of midwifery students in learning, to evaluate the simulation design and educational effectiveness, it was planned to use the scenario-based near-realistic simulation method in the form of randomized control-intervention quantitatively, and in qualitative design to evaluate the students' views on the method and educational effectiveness. The research will make it easier for midwifery students to intervene with the patient in a shorter time, with confidence and with sufficient clinical skills, and patient safety will be increased. In addition, it will allow the reduction of erroneous clinical practices and malpractices. This study aims to evaluate the satisfaction and self-confidence status of midwifery students and the educational effectiveness of the scenario-based simulation method with high closeness to reality in GDM management and to examine the opinions about this method to fill the gap in the literature.

研究概览

研究类型

介入性

注册 (预期的)

78

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人
  • 年长者

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Agreeing to participate in the research,
  • Being a midwifery 3rd year student and taking the "risky pregnancy" course,
  • Those who have no previous clinical experience in GDM (Health College, Health Vocational High School Graduate, etc.)

Exclusion Criteria:

  • To fill in the data collection forms of the study incompletely,
  • Not participating in all applications of simulation training with high proximity to reality,
  • Desire to leave the research.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:诊断
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:gestational diabetes management simulation
Gestational diabetes management of midwifery students with a simulator
无干预:no intervention will be made

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
information evaluation form
大体时间:immediately before simulation
The information evaluation form is in a multiple-choice format consisting of 25 questions by scanning the literature by the researchers. Each question is worth 4 points.
immediately before simulation
information evaluation form
大体时间:7 weeks after the first simulation application
The information evaluation form is in a multiple-choice format consisting of 25 questions by scanning the literature by the researchers. Each question is worth 4 points.
7 weeks after the first simulation application
学生学习满意度和自信心量表
大体时间:在第一次模拟应用后立即
该量表是一个包含 13 个项目的测量工具,旨在衡量学生在练习期间对模拟和自信心的满意度。 Likert 5 点计分,强烈不同意 1 分,不同意 2 分,犹豫不决 3 分,同意 4 分,非常同意 5 分。
在第一次模拟应用后立即
学生学习满意度和自信心量表
大体时间:在第二次模拟应用后立即
该量表是一个包含 13 个项目的测量工具,旨在衡量学生在练习期间对模拟和自信心的满意度。 Likert 5 点计分,强烈不同意 1 分,不同意 2 分,犹豫不决 3 分,同意 4 分,非常同意 5 分。
在第二次模拟应用后立即
Student Satisfaction and Self-Confidence Scale in Learning
大体时间:immediately after the third simulation application
The scale is a 13-item measurement tool designed to measure student satisfaction with simulation and self-confidence during practices. It is a 5-point Likert type and is scored as strongly disagree 1, disagree 2, undecided 3, agree 4, strongly agree 5.
immediately after the third simulation application
仿真设计规模
大体时间:在第一次模拟应用后立即
对干预组应用和设计的模拟方法用于对参与者的评估。 仿真设计量表共20个项目。 量表的评估分两个阶段进行。 在第一阶段,为了评估模拟方法中使用的项目是否以对参与者最好的方式给出,他们表示为非常不同意、不同意、未决定、同意、非常同意。 在第二阶段,有陈述将确定量表项目对参与者的重要性级别,不重要、部分重要、未定、重要、非常重要。 在评估阶段,量表得分的计算方法是将总分和子维度的总和除以项目数。
在第一次模拟应用后立即
仿真设计规模
大体时间:在第二次模拟应用后立即
对干预组应用和设计的模拟方法用于对参与者的评估。 仿真设计量表共20个项目。 量表的评估分两个阶段进行。 在第一阶段,为了评估模拟方法中使用的项目是否以对参与者最好的方式给出,他们表示为非常不同意、不同意、未决定、同意、非常同意。 在第二阶段,有陈述将确定量表项目对参与者的重要性级别,不重要、部分重要、未定、重要、非常重要。 在评估阶段,量表得分的计算方法是将总分和子维度的总和除以项目数。
在第二次模拟应用后立即
Simulation Design Scale
大体时间:immediately after the third simulation application
The simulation method applied and designed to the intervention group is used in the evaluation of the participants. The simulation design scale consists of 20 items in total. Evaluation of the scale is done in two stages. In the first stage, in order to evaluate whether the items used in the simulation method were given in the best way for the participant, they were expressed as strongly disagree, disagree, undecided, agree, strongly agree. In the second stage, there are statements that will determine the level of importance of the scale items for the participant, not important, partially important, undecided, important, very important. In the evaluation phase, the scale score is calculated by dividing the total and the total of the sub-dimensions by the number of items.
immediately after the third simulation application

次要结果测量

结果测量
措施说明
大体时间
Semi-Structured Focus Group Training Activity Evaluation Form
大体时间:7 weeks after starting the study
It is a form consisting of 5 semi-structured questions created by the researchers after a comprehensive literature search in order to evaluate the simulation training effectiveness. With these questions, it was aimed to determine the strengths and weaknesses of training with the simulation method regarding GDM management, the opportunities/opportunities it provides and the threats and dangers created by this method.
7 weeks after starting the study

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (预期的)

2022年4月19日

初级完成 (预期的)

2022年4月19日

研究完成 (预期的)

2024年5月31日

研究注册日期

首次提交

2022年4月17日

首先提交符合 QC 标准的

2022年4月23日

首次发布 (实际的)

2022年4月29日

研究记录更新

最后更新发布 (实际的)

2022年4月29日

上次提交的符合 QC 标准的更新

2022年4月23日

最后验证

2022年4月1日

更多信息

与本研究相关的术语

其他研究编号

  • sbu_yılmaz38

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

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