跳至主要内容
临床试验/NCT05628207
NCT05628207
招募中
不适用

Evaluation of the SCALED (SCaling AcceptabLE cDs) Approach for the Implementation of Interoperable CDS for Venous Thromboembolism Prevention - CDS Data

University of Minnesota2 个研究点 分布在 1 个国家目标入组 15,000 人2023年5月16日

概览

阶段
不适用
干预措施
Observational
疾病 / 适应症
Traumatic Brain Injury
发起方
University of Minnesota
入组人数
15000
试验地点
2
主要终点
primary effectiveness outcome
状态
招募中
最后更新
8天前

概览

简要总结

This project will adapt a currently deployed Clinical Decision Support (CDS) system to deliver a VTE prevention guideline for adult patients with traumatic brain injury (TBI). We believe this is an ideal PCOR use case given PCORI's continued effort to combat VTE in trauma and our experience previously implementing this guideline. The Our overall goal is to successfully scale, evaluate, and maintain an interoperable TBI CDS across 7 total institutions.

注册库
clinicaltrials.gov
开始日期
2023年5月16日
结束日期
2026年7月31日
最后更新
8天前
研究类型
Observational
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • age 18 and older
  • admitted with a TBI

排除标准

  • Patients who die within 24 hours of hospital admission and patients documented as "comfort cares" during the first 72 hours of hospitalization or with mild TBI will be excluded from final analysis.

研究组 & 干预措施

4 hospitals using CDS TBI

healthcare system leveraging the rigorous approach, SCALED (SCaling AcceptabLE cDs), to guide CDS scaling across the system in VTE prevention.

干预措施: Observational

3 hospitals not using CDS TBI (control)

healthcare system not leveraging the rigorous approach, SCALED (SCaling AcceptabLE cDs), to guide CDS scaling across the system in VTE prevention.

干预措施: Observational-control

结局指标

主要结局

primary effectiveness outcome

时间窗: 2 years and a half

VTE event rate

Evaluate implementation strategy guided by the EPIS Implementation

时间窗: 2 years and a half

the number of patients that received treatment according to the best practice guideline and the % adherence to the guideline per site

研究点 (2)

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