- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03902873
The Effect of a Real-time Audiovisual Feedback System on CPR Quality
July 10, 2023 updated by: Ho Geol Ryu, Seoul National University Hospital
The Effect of a Real-time Audiovisual Feedback System on CPR Quality During In-hospital Cardiac Arrest: A Prospective Observational Study
The investigators will evaluate the effect of a real-time audiovisual feedback system on CPR quality during in-hospital cardiac arrest.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
300
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Agree
-
Seoul, Agree, Korea, Republic of, 110-744
- Seoul National University Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Patients over 17 years old who require cardiopulmonary resuscitation in a medical or surgical intensive care units
Exclusion Criteria:
- Patients less than 18 years
- Patients with Do Not Resuscitate order
- Patients who require cardiopulmonary resuscitation outside a medical or surgical intensive care unit
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Sequential Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: usual compression
A group who get no real-time audiovisual feedback from the R Series® Monitor/Defibrillator (Zoll medical).
|
|
|
Active Comparator: real-time audiovisual feedback
A group who get the real-time audiovisual feedback from the R Series® Monitor/Defibrillator (Zoll medical).
|
During the chest compressions, doctors receive audiovisual feedback on the depth and speed of the appropriate chest compressions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
chest compression fraction
Time Frame: 2 min
|
the percentage of time in which chest compression are done by rescuers during a cardiopulmonary resuscitation
|
2 min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Ho Geol Ryu, Ph.D., Seoul National University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 20, 2018
Primary Completion (Actual)
March 20, 2023
Study Completion (Actual)
March 20, 2023
Study Registration Dates
First Submitted
April 2, 2019
First Submitted That Met QC Criteria
April 2, 2019
First Posted (Actual)
April 4, 2019
Study Record Updates
Last Update Posted (Actual)
July 12, 2023
Last Update Submitted That Met QC Criteria
July 10, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- Audiovisual feedback_CPR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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