跳至主要内容
临床试验/NCT02039297
NCT02039297已完成不适用

Patient Centered Cloud-based Electronic System: Ambient Warning and Response Evaluation (ProCCESs AWARE)

Mayo Clinic6 个研究点 分布在 1 个国家目标入组 7,813 人开始时间: 2013年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
7,813
试验地点
6
主要终点
Adherence to process of care

研究概览

简要总结

In this multicenter project, we will introduce AWARE (electronic interface) Using a cloud-based technology . The goal of this project is to improve compliance with best practice through the use of a new acute care interface with built-in tools for error prevention, practice surveillance and reporting (ProCCESs AWARE - Patient Centered Cloud-based Electronic System: Ambient Warning and Response Evaluation).The goal of this project is to develop and test a novel acute care interface with built-in tools for error prevention, practice surveillance, decision support and reporting (ProCCESs AWARE - Patient Centered Cloud-based Electronic System: Ambient Warning and Response Evaluation). In preliminary studies, these novel informatics supports built on an advanced understanding of cognitive and organizational ergonomics, have significantly decreased the cognitive load of bedside providers and reduced medical errors. Using a cloud-based technology, AWARE will be uniformly available on either mobile or fixed computing devices and applied in a standardized manner in medical and surgical ICUs of five geographically diverse acute care hospitals predominantly serving Medicare and Medicaid patients. The impact of ProCCESs AWARE on processes of care and outcomes in study ICUs; expected to enroll more than 10,000 critically ill patients during the study period.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
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
否

入选标准

  • •For the Primary Objective, all critically ill adult patient admitted to an ICU participating in the study will be eligible.

排除标准

  • •For the Primary Objective, all children younger than 18years of age will be excluded.

研究组 & 干预措施

No Intervention: Baseline arm

Other

Pre and post design (same arm)

干预措施: Patient Centered Cloud-based Electronic System: Ambient Warning and Response Evaluation (Other)

结局指标

主要结局

Adherence to process of care

时间窗: Participants will be followed for the duration of ICU stay, an expected average of 3 days

Adherence to best practice for daily intensive care rounds. Appropriate shock resuscitation Appropriate sepsis treatment Appropriate mechanical ventilation Appropriate peptic ulcer, deep vein thrombosis and infectious disease prophylaxis etc.

次要结局

  • Patient outcomes(Hospital length of stay - 2 weeks)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Brian W. Pickering, M.B., B.Ch.

Consultant

Mayo Clinic

研究点 (6)

Loading locations...

相似试验