Clinical Trials Directory

Trials / Completed

CompletedNCT01245699

MIHS Emergency Department CPR Quality Improvement Project

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
115 (actual)
Sponsor
Valleywise Health · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The investigators will quantify the quality of chest compressions provided in the Emergency Department and determine whether the quality of chest compressions is related to patient outcome. The quality of chest compressions and patient outcomes will be assessed both before and after the introduction of audiovisual feedback in real time.

Detailed description

The Emergency Department will be using E-series unit manufactured by ZOLL Medical Group (Chelmsford, MA). These units are equipped with an accelerometer-based system that allows for measurement of chest compression depth and rate. These units are also equipped with RealCPRHelp, and FDA-approved technology that provides real-time audiovisual feedback to providers on the quality of chest compressions. In the first phase of the project, the ED providers will utilize the E-series units to treat all patients requiring chest compressions.

Conditions

Interventions

TypeNameDescription
BEHAVIORALscenario-based training, real-time audiovisual CPR feedback, and post-event debriefingscenario-based training for CPR, real-time audiovisual CPR feedback using R Series monitor-defibrillator during treatment, and post-event debriefing

Timeline

Start date
2010-06-09
Primary completion
2015-11-05
Completion
2016-03-09
First posted
2010-11-22
Last updated
2019-04-26
Results posted
2019-04-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01245699. Inclusion in this directory is not an endorsement.