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    【ChiCTR2500099134】Effect of an evidence-based assessment instrument to minimize the use of physical restraint in general adult ward settings in Hong Kong: A cluster randomized controlled trial

    基本信息
    登记号

    ChiCTR2500099134

    试验状态

    尚未开始

    药物名称

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    药物类型

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    规范名称

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    首次公示信息日的期

    2025-03-19

    临床申请受理号

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    靶点

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    适应症

    Nil

    试验通俗题目

    Effect of an evidence-based assessment instrument to minimize the use of physical restraint in general adult ward settings in Hong Kong: A cluster randomized controlled trial

    试验专业题目

    Effect of an evidence-based assessment instrument to minimize the use of physical restraint in general adult ward settings in Hong Kong: A cluster randomized controlled trial

    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

    The objectives of this research are to evaluate the effect of the evidence-based assessment instrument to minimize the use of PR in general adult ward settings, and the process evaluation and satisfaction of the evidence-based assessment instrument when applying in general adult ward settings in Hong Kong.

    试验分类
    试验类型

    整群随机分组

    试验分期

    其它

    随机化

    A single blinded cluster randomized controlled trial will be conducted in a total of eight wards within the department of Medicine & Geriatrics (M&G), the department of Orthopaedics & Traumatology (O&T), and the Department of Surgery (SUR) from 8th April to 9th June 2025 at UCH. Two wards from O&T and SUR, along with four wards from M&G, will be randomly assigned using simple random sampling.

    盲法

    A single blinded cluster randomized controlled trial will be conducted as the patient does not know which group they are allocated.

    试验项目经费来源

    Nil

    试验范围

    /

    目标入组人数

    932

    实际入组人数

    /

    第一例入组时间

    2025-03-25

    试验终止时间

    2025-06-09

    是否属于一致性

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    入选标准

    Participants aged 18 or above and admitted to the general adult ward settings at the research sites within the hospital are eligible to participate in the study. All nurses who provide direct patient care, will be included for the process evaluation and satisfaction review.；

    排除标准

    For the clinical study, there are no exclusion criteria, as all patients are under treatment and care during hospitalization. Participation in the evaluation is voluntary for healthcare providers who wish to give feedback and participate in the survey.；

    研究者信息
    研究负责人姓名
    试验机构

    United Christian Hospital, Hong Kong Hospital Authority

    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

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