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Pediatric Resuscitation With Feedback Devices (CPR_NURSE)

I

International Institute of Rescue Research and Education

Status

Unknown

Conditions

Cardiac Arrest

Treatments

Device: The CPR PRO APP
Device: TrueCPR
Device: Standard BLS
Device: The CPREazy
Device: The CardioPump

Study type

Interventional

Funder types

Other

Identifiers

NCT02294721
CPR/2014/10

Details and patient eligibility

About

The aim of this study was to compare four different CPR feedback devices to standard BLS in terms of the quality of single rescuer pediatric resuscitation. Therefore, the investigators hypothesis was that there would be no difference between CPR methods in terms of chest compression quality parameters.

Full description

Cardiac arrest is a leading cause of death worldwide. High-quality chest compressions are of paramount importance for survival and good neurological outcome. Unfortunately, even health professionals have difficulty performing effective CPR. Chest compression (CC) is often too shallow, compression ratio is inadequate, and hands-off time is too long. CPR feedback devices might be an option for rescuers to in order to increase CC efficiency.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • give voluntary consent to participate in the study
  • medical profession (nurses)

Exclusion criteria

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

200 participants in 2 patient groups

Without feedback
Experimental group
Description:
Participants compress the chest of the manikin without CPR feedback device
Treatment:
Device: Standard BLS
With feedback
Experimental group
Description:
Participants compress the chest of the manikin with CPR feedback device.
Treatment:
Device: The CardioPump
Device: TrueCPR
Device: The CPREazy
Device: The CPR PRO APP

Trial contacts and locations

1

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Central trial contact

Andrzej Kurowski

Data sourced from clinicaltrials.gov

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