ChiCTR2500099134尚未招募Unknown
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
未提供1 个研究点 分布在 1 个国家目标入组 1,864 人开始时间: 2025年3月25日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 入组人数
- 1,864
- 试验地点
- 1
- 主要终点
- Crude and absolute prevalent number per day
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 主要目的
- 整群随机分组
- 盲法
- Single
入排标准
- 年龄范围
- 18 至 —（—）
- 性别
- All
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.
研究组 & 干预措施
Control group
Convention record form
Intervention group
The evidence-based assessment instrument
结局指标
主要结局
Crude and absolute prevalent number per day
时间窗: Daily
次要结局
- overall satisfaction
- the duration of physical restraint use
- safety incidents, including accidental catheter removal, falls, length of stay during hospitalization
研究者
研究点 (1)
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