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Family ICU Delirium Detection Study

NCT03379129 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 147

Last updated 2019-05-16

No results posted yet for this study

Summary

To evaluate the validity, reliability, and acceptability of employing family-administered delirium detection tools in the critically ill. The ultimate goal of this project is to improve the care of critically ill patients by creating valid, earlier, and patient and family-centered prevention, recognition, and management of delirium.

Conditions

  • Delirium

Sponsors & Collaborators

  • Alberta Health services

    collaborator OTHER

  • University of Calgary

    lead OTHER

Principal Investigators

  • Kirsten M Fiest, PhD · University of Calgary

  • Henry T Stelfox, MD, PhD · University of Calgary

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-06
Primary Completion
2018-09-14
Completion
2018-09-14

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03379129 on ClinicalTrials.gov