跳至主要内容
临床试验/NCT03360474
NCT03360474撤回不适用

The Implementation of a Delirium Screening and Intervention Protocol for Critically Ill Patients

University of Miami0 个研究点开始时间: 2018年6月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
ICU Length of Stay (LOS)

研究概览

简要总结

The purpose of this project is to improve patient outcomes in individuals affected by cancer, through the implementation of a delirium screening and treatment protocol in the ICU setting. The hypothesis is that patients who receive an accurate and early diagnosis of delirium coupled with a standardized intervention protocol will demonstrate improved patient outcomes as evidenced by fewer days spent in the ICU, fewer days spent in the hospital (overall length of stay) and the need for less sedative medication throughout their ICU stay as compared to patient data prior to the implementation of a delirium protocol.

研究设计

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

  • Patients will be included into the study who:
  • Are over 18 years old
  • Speak and read English
  • Are admitted to the Sylvester Comprehensive Cancer Center intensive care unit in the first 60 days following implementation of the delirium protocol; approximately 10 patients per month.
  • Patient data via electronic medical record (EMR) for all patients who were admitted to the Sylvester Comprehensive Cancer Center intensive care unit up to 60 days prior to the implementation of the delirium protocol.

排除标准

  • This study will exclude:
  • Patients who are unable to speak and read English
  • Patients who are unable to provide written consent to participate.
  • Patient data via EMR for any patients who were admitted to the Sylvester Comprehensive Cancer Center intensive care unit prior to 60 days before to the implementation of the delirium protocol.

结局指标

主要结局

ICU Length of Stay (LOS)

时间窗: 60 days

Patient's length of stay in the ICU

次要结局

  • Overall LOS in hospital(60 days)
  • Sedation Medication(60 days)

研究者

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

Maria Rueda-Lara

Assistant Profesor of Clinical Psychiatry

University of Miami

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