CPR Feedback Devices

NCT02293200 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2014-11-18

No results posted yet for this study

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.

Conditions

  • Cardiac Arrest

Interventions

DEVICE

Standard BLS

basic life support without any feedback device

DEVICE

TrueCPR

CPR with feedback device

Sponsors & Collaborators

  • International Institute of Rescue Research and Education

    lead OTHER

Principal Investigators

  • Lukasz Szarpak · Institute of Cardiology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2014-12-31
Completion
2014-12-31

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02293200 on ClinicalTrials.gov