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

NACompletedINTERVENTIONAL
Enrollment

166

Participants

Timeline

Start Date

February 14, 2017

Primary Completion Date

November 10, 2018

Study Completion Date

December 31, 2018

Conditions
Sleep Quality
Interventions
BEHAVIORAL

Risk Stratification

Every night, subjects will be risk stratified into low-risk or medium- to high-risk using a physiologic risk score, eCART. Subjects who meet the low-risk criteria will not be woken up for routine nighttime vitals (typically at midnight and at 4 am). However, subjects will continue to be woken up for laboratory draws, procedures, or treatments as per usual. Subjects who are medium- to high-risk will continue to be woken up at night for routine nighttime vitals. Alarms for all subjects, including low-risk subjects, will continue to alert nurses in real-time. If the primary nurse of a low-risk subject is alerted of an alarm, the nurse will have to go into the subject's room to turn off the alarm and therefore check on the patient.

BEHAVIORAL

Usual Care

The subject will continue to receive routine vital sign measurements and charting, standard for the ward or according to the physician orders, including routine spot-check vital signs, regardless of risk level.

Trial Locations (1)

60637

University of Chicago, Chicago

All Listed Sponsors
collaborator

EarlySense Ltd.

INDUSTRY

lead

University of Chicago

OTHER

NCT03010774 - Identifying At-Risk Patients and Predicting Deterioration of In-Patients Using Continuous Heart Rate, Respiratory Rate, and Movement Monitoring | Biotech Hunter | Biotech Hunter