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    【ChiCTR2000031105】该研究尚未获得伦理委员会批准。请于批准后才开始纳入参试者,并与我们联系上传批件。The effectiveness of Crew Resource Management based Simulation Training (CRM-ST) program in improving student midwives' performance

    基本信息
    登记号

    ChiCTR2000031105

    试验状态

    尚未开始

    药物名称

    /

    药物类型

    /

    规范名称

    /

    首次公示信息日的期

    2020-03-22

    临床申请受理号

    /

    靶点

    /

    适应症

    助產士學生培訓

    试验通俗题目

    该研究尚未获得伦理委员会批准。请于批准后才开始纳入参试者,并与我们联系上传批件。The effectiveness of Crew Resource Management based Simulation Training (CRM-ST) program in improving student midwives' performance

    试验专业题目

    The effectiveness of Crew Resource Management based Simulation Training (CRM-ST) program in improving student midwives' performance

    申办单位信息
    申请人联系人
    申请人名称
    联系人邮箱
    联系人邮编

    联系人通讯地址
    临床试验信息
    试验目的

    This study investigates the effectiveness of a Crew Resource Management based Simulation Training (CRM-ST) program in improving student midwives performance in managing postpartum haemorrhage.

    试验分类
    试验类型

    随机平行对照

    试验分期

    其它

    随机化

    The participants will be randomly assigned to either the control or the intervention group. The research assistant will generate the random number sequence. Randomization is conducted by using consecutively numbered and sealed opaque envelopes containing group allocations.

    盲法

    Open label

    试验项目经费来源

    醫院管理局

    试验范围

    /

    目标入组人数

    58

    实际入组人数

    /

    第一例入组时间

    2020-04-01

    试验终止时间

    2021-03-31

    是否属于一致性

    /

    入选标准

    - Student midwives who have completed at least 12 months of midwifery training program as accredited by the Midwives Council of Hong Kong; - Student midwives who have received a theoretical lecture on postpartum haemorrhage; - Student midwives who are able to read and understand English; - Student midwives who are willing to participate this study.;

    排除标准

    - Those who had previous training in CRM; - Those who refuse to participate.;

    研究者信息
    研究负责人姓名
    试验机构

    No

    研究负责人电话
    研究负责人邮箱
    研究负责人邮编

    /

    联系人通讯地址

    No的其他临床试验

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