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The Effect of Real Time Analytics on Adverse Events Among Hospitalized Patients

NCT04674098 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2024-06-07

No results posted yet for this study

Summary

This study will examine the effect of providing nurses with continuous, remote, real-time monitoring of their patient's vital signs and MEWS scores using the BAS on the occurrence of adverse events, admissions to the ICU, hospital length of stay and activation of the rapid response team among patients on non-intensive care hospital units. A longitudinal study will measure the outcome variables among an estimated 60 patients per month during 6 month intervals when the BAS is not and is available to the nursing staff.

Conditions

  • Hospital Acquired Condition

Interventions

DEVICE

The Beat Analytics System (BAS)

There are three subsystems to the BAS; data aggregation, data analysis and data presentation.

Sponsors & Collaborators

  • Bob Topp

    lead OTHER

Principal Investigators

  • Robert Topp, PhD · College of Nursing

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-04-01
Primary Completion
2022-01-30
Completion
2022-01-30
FDA Device
Yes

Countries

  • United States

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 NCT04674098 on ClinicalTrials.gov