How to Learn Cardiopulmonary Resuscitation

April 27, 2020 updated by: Łukasz Szarpak, Lazarski University

A Comparison of Two Chest Compression Techniques Among Laypersons. A Prospective, Randomized Simulation Study

the aim of the study is to evaluate two methods of teaching cardiopulmonary resuscitation in the context of chest compression quality. We will evaluate the usefulness of the application cpr feedback device (CPRMeter) for quality of chest compression.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

330

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

  • Poland
    • Masovia
      • Warsaw, Masovia, Poland, 02-662
        • Lazarski Univerisity

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

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • give voluntary consent to participate in the study
  • no medical experience

Exclusion Criteria:

  • not meet the above criteria
  • wrist or low back diseases
  • pregnancy

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: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: SINGLE_GROUP
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Chest compression without cpr feedback device
teaching resuscitation without application of cpr feedback device
Other: Manual chest compression
Manual chest compression
EXPERIMENTAL: Chest compression with cpr feedback device
teaching resuscitation with application of CPRMeter - cpr feedback device
Device: CPRMeter
teaching resuscitation with application of cpr feedback device

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
chest compressions effectiveness
Time Frame: 1 day
the percentage of correct chest compressions relative to the total number of chest compressions
1 day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
depth
Time Frame: 1 day
correct depth according to European Resuscitation Council 2015 guidelines for cardiopulmonary resuscitation
1 day
pressure point
Time Frame: 1 day
correct pressure point according to European Resuscitation Council 2015 guidelines for cardiopulmonary resuscitation
1 day
Complete pressure release
Time Frame: 1 day
Complete pressure release measure by manikin software
1 day
Rate of chest compression
Time Frame: 1 day
correct chest compressions rate according to European Resuscitation Council 2015 guidelines for cardiopulmonary resuscitation
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Lazarski University

Collaborators

The Cleveland Clinic
Wroclaw Medical University

Investigators

  • Study Chair: Lukasz Szarpak, Lazarski University

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)

July 20, 2019

Primary Completion (ACTUAL)

August 3, 2019

Study Completion (ACTUAL)

August 3, 2019

Study Registration Dates

First Submitted

July 29, 2019

First Submitted That Met QC Criteria

July 30, 2019

First Posted (ACTUAL)

July 31, 2019

Study Record Updates

Last Update Posted (ACTUAL)

April 28, 2020

Last Update Submitted That Met QC Criteria

April 27, 2020

Last Verified

April 1, 2020

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • CPR_NET

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

after finish study, we will share data on https://repod.pon.edu.pl/pl/

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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