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Clinical Trials/NCT02293200
NCT02293200UnknownNot Applicable

TWO METHODS OF TRAINING TO IMPROVE CHEST COMPRESSION EFFECITVENESS BY MEDICAL STUDENTS AND BYSTANDERS: A Randomized Trial

International Institute of Rescue Research and Education2 sites in 1 country200 target enrollmentStarted: November 1, 2014Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
200
Locations
2
Primary Endpoint
Effective compressions compression with correct depth (40-50mm), correct hand position and complete decompressions
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The aim of the study was to compare two methods of training in CPR, standard basic life support and CPR using CPR feedback device.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Give voluntary consent to participate in the study

Exclusion Criteria

  • •Not meet the above criteria
  • •Wrist or low back diseases

Outcomes

Primary Outcomes

Effective compressions compression with correct depth (40-50mm), correct hand position and complete decompressions

Time Frame: 1 month

effective compressions was defined as compression with correct depth (40-50mm), correct hand position and complete decompressions

Secondary Outcomes

  • effective compressions ratio effective compressions [%] multiplied by flow time [%](1 month)
  • Flow time sum of all periods during which chest compressions were performed.(1 month)
  • absolute hands-off time sum of all periods without chest compressions or ventilation(1 month)
  • Compression depth compression in correct depth (40-50mm) measured by the software is connected to the manikin and computer(1 month)

Investigators

Sponsor
International Institute of Rescue Research and Education
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lukasz Szarpak

Lukasz Szarpak

National Institute of Cardiology, Warsaw, Poland

Study Sites (2)

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