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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

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基本信息

登记号

ChiCTR2500099134

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

2025-03-19

临床申请受理号

靶点

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

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申请人名称

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联系人邮编

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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

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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

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

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试验机构

United Christian Hospital, Hong Kong Hospital Authority

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