跳至主要内容
临床试验/NCT01612091
NCT01612091撤回不适用

The Monitoring Messenger: Mobile Patient Monitoring for the Pediatric Intensive Care Unit

University of British Columbia2 个研究点 分布在 1 个国家开始时间: 2013年11月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
Accuracy of priority assignment in triaging task

研究概览

简要总结

The Mobile Messenger is a unified, portable and intelligent device that integrates information from multiple patient monitors, mechanical ventilators, infusion pumps and clinical information systems on a mobile platform. It will allow nurses, respiratory therapists and physicians to continuously monitor and coordinate care of critically ill patients. This study will use a participatory design process to guide the design of an integrated mobile device. Next, we will evaluate the proposed device in a simulated ICU setting.

详细描述

There are a limited number of nurses, respiratory therapists and physicians in an ICU at a given time. To make decisions and plan therapies, these clinicians need to observe, assimilate and interpret a vast array of information originating from various devices located on the bedsides of multiple patients. Several shortcomings in existing technology limit their abilities: a) the fixed location of monitoring devices at the bedside; b) information overload from a multitude of devices, each with its own display; c) the lack of integration and interaction between these devices; d) the use of visually cumbersome displays, which were historically created for monitoring during anesthesia but never optimized for users in the ICU; and e) lack of context specific information (such as historical trends) to support patient data interpretation and clinical decision making.

This project proposes to address these challenges in ICU monitoring by developing a unified, portable, and intelligent device: the Monitoring Messenger. By integrating information from multiple monitoring devices, mechanical ventilators, infusion pumps and clinical information systems on a mobile device (tablet PC or smart phone); the Monitoring Messenger will allow nurses, respiratory therapists and physicians on or off-site, to continuously monitor critically ill patients, thereby increasing patient safety.

The proposed experiment will have two parts: Part I - Participatory design and Part II - Simulation Experiment.

In Part I - Participatory Design. Participatory design an inter-professional team of nurses, physicians, designers, engineers, and human factors experts will follow a user-centered design process to obtain the system requirements, and obtain feedback during the rapid prototyping phase of prototype development. While we expect the resulting prototype to be easy to use, support decision making, improve awareness of the patient's condition by health care providers and reduce mental workload, this methodology is not hypothesis driven.

Part II - Simulation Experiment. In simulated ICU scenarios, the critical care physicians, nurses, and respiratory therapists will prioritize the care of critically ill patients. We expect them to do so more accurately with the use of Monitoring Messenger than with their regular tool (monitors, paper records etc). A potential outcome would be a decrease in mental workload as well as an increase in situational awareness.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Staff pediatric critical care physicians, pediatric critical care fellow physicians, registered pediatric nurses and respiratory therapists will be eligible to participate in this study
  • Subjects willing to provide informed consent

排除标准

  • Inability/failure to provide informed consent.
  • Nursing students and resident physicians are not eligible
  • For Part II - Simulation Experiment only: Failure to complete the post-training quiz more than twice.
  • Evaluation will be immediately discontinued at request of subject at any point during the study.

研究组 & 干预措施

Monitoring Messenger

Experimental

干预措施: Monitoring Messenger (Device)

Control

Active Comparator

Traditional tools (monitors, paper records)

干预措施: Traditional tools (Device)

结局指标

主要结局

Accuracy of priority assignment in triaging task

时间窗: Up to 1 hour

Accuracy will be measured by matching of the participants triage priority ranking with the previously defined expert ranking.

次要结局

  • Requirements for design of the mobile device(Up to 2 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mark Ansermino

Principle Investigator

University of British Columbia

研究点 (2)

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