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The Effect of a Real-time Audiovisual Feedback System on CPR Quality

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03902873
Recruitment Status : Recruiting
First Posted : April 4, 2019
Last Update Posted : September 25, 2019
Sponsor:
Information provided by (Responsible Party):
Ho Geol Ryu, Seoul National University Hospital

Brief Summary:
The investigators will evaluate the effect of a real-time audiovisual feedback system on CPR quality during in-hospital cardiac arrest.

Condition or disease Intervention/treatment Phase
Cardiopulmonary Resuscitation Other: Real-time audiovisual feedback Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 300 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Other
Official Title: The Effect of a Real-time Audiovisual Feedback System on CPR Quality During In-hospital Cardiac Arrest: A Prospective Observational Study
Actual Study Start Date : November 20, 2018
Estimated Primary Completion Date : October 20, 2021
Estimated Study Completion Date : March 20, 2022

Resource links provided by the National Library of Medicine


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).
Other: Real-time audiovisual feedback
During the chest compressions, doctors receive audiovisual feedback on the depth and speed of the appropriate chest compressions.




Primary Outcome Measures :
  1. chest compression fraction [ Time Frame: 2 min ]
    the percentage of time in which chest compression are done by rescuers during a cardiopulmonary resuscitation



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03902873


Contacts
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Contact: Hannah Lee, Ph.D. +821077506056 closerthan@gmail.com

Locations
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Korea, Republic of
Seoul National University Hospital Recruiting
Seoul, Agree, Korea, Republic of, 110-744
Contact: Hogeol Ryu, MD, PhD    82-2-2072-2469    hogeol@gmail.com   
Contact: Hannah Lee, MD    82-2-2072-3538    closerthan@gmail.com   
Principal Investigator: Hogeol Ryu, MD, PhD         
Seoul National University Hospital Recruiting
Seoul, Agree, Korea, Republic of, 110-744
Contact: Hannah Lee    +821077506056    closerthan@gmail.com   
Contact: Ho Geol Ryu    +82220722469    hogeol@gmail.com   
Sponsors and Collaborators
Seoul National University Hospital
Investigators
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Principal Investigator: Ho Geol Ryu, Ph.D. Seoul National University Hospital
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Responsible Party: Ho Geol Ryu, Associate professor, Seoul National University Hospital
ClinicalTrials.gov Identifier: NCT03902873    
Other Study ID Numbers: Audiovisual feedback_CPR
First Posted: April 4, 2019    Key Record Dates
Last Update Posted: September 25, 2019
Last Verified: September 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No