跳至主要内容
临床试验/NCT02458872
NCT02458872已完成不适用

Impact of a Data-driven Monitor Alarm Reduction Strategy Implemented in Safety Huddles

Children's Hospital of Philadelphia1 个研究点 分布在 1 个国家目标入组 77,280 人开始时间: 2015年7月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
77,280
试验地点
1
主要终点
Change from baseline in the unit-wide rate of alarms per patient-day at 44 weeks

研究概览

简要总结

This is a pragmatic, paired, cluster-randomized controlled trial evaluating the impact of a safety huddle-based intervention on physiologic monitor alarm rates on pediatric inpatient units.

详细描述

Hospital physiologic monitors can alert clinicians to early signs of physiologic deterioration, and thus have great potential to be life-saving. However, monitors generate frequent alarms, most of which are non-actionable.

When clinicians become overburdened with alarms, they begin to exhibit alarm fatigue: responding more slowly to alarms or ignoring alarms entirely. In this protocol the investigators outline the methods they will use to evaluate the impact of a safety huddle-based intervention on physiologic monitor alarm rates using a pragmatic, paired, cluster-randomized controlled trial with the intervention delivered at the unit level. This work is considered quality improvement research, and some of the approaches described in this protocol are from the field of quality improvement.

Currently, at most hospitals data like this on the numbers of alarms that patients generate are only available to researchers with the software tools needed to interrogate and record data from the monitor network. The goal of this proposal is to bring this data to the safety huddles occurring daily on inpatient units in an accessible format to help teams make informed decisions about monitoring and minimize the potential of harm from alarm fatigue.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Intervention Arm

Experimental

Safety huddle alarm intervention.

干预措施: safety huddle alarm intervention (Behavioral)

Control Arm

No Intervention

Usual care.

结局指标

主要结局

Change from baseline in the unit-wide rate of alarms per patient-day at 44 weeks

时间窗: Baseline and 44 weeks

次要结局

  • Pre-post huddle patient-level difference in differences of alarm rates(The 24 hours before a safety huddle opportunity versus the 24 hours before a safety huddle opportunity)
  • Implementation outcomes(Within 4 hours after the huddle intervention occurred)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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