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Clinical Trials/NCT03360474
NCT03360474
Withdrawn
Not Applicable

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

University of Miami0 sitesJune 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Delirium
Sponsor
University of Miami
Primary Endpoint
ICU Length of Stay (LOS)
Status
Withdrawn
Last Updated
7 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
June 2018
End Date
December 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Maria Rueda-Lara

Assistant Profesor of Clinical Psychiatry

University of Miami

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

ICU Length of Stay (LOS)

Time Frame: 60 days

Patient's length of stay in the ICU

Secondary Outcomes

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

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