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Identifying At-Risk Patients and Predicting Deterioration of In-Patients Using Continuous Heart Rate, Respiratory Rate, and Movement Monitoring

Sleep Quality Clinical Trial

Official title:
Identifying At-Risk Patients and Predicting Deterioration of In-Patients Using Continuous Heart Rate, Respiratory Rate, and Movement Monitoring

Clinical Trial Summary

Currently, all patients in the hospital are woken up throughout the night to check for vital signs, no matter how sick they are. The investigators are doing this study to determine whether skipping routine vital sign checks at night improves participant sleep quality and satisfaction without increasing the risk of adverse events.

Clinical Trial Description

The purpose of this study is:

1. To determine the correlation between subjective and objective sleep quality measures.

2. To compare the objective and subjective measures of sleep quality and satisfaction between the intervention group and the control group.

3. To compare the adverse event rates in the intervention group and the control group, defined as ICU transfer or cardiac arrest occurring within 24 hours of risk stratification. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03010774
Study type Interventional
Source University of Chicago
Contact
Status Completed
Phase N/A
Start date February 14, 2017
Completion date December 31, 2018
View Details
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