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CompletedNCT02281903PRFDUpdated Nov 18, 2014

Pediatric Resuscitation With Feedback CPR Devices

An interventional study of The TrueCPR feedback device and Standard BLS in Cardiac Arrest, sponsored by International Institute of Rescue Research and Education. Completed at 1 site in Poland. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2014-11-18.

Sponsored by International Institute of Rescue Research and Education · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
132
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The aim of this study was to compare the TrueCPR feedback device (with metronome) to standard basic life support (BLS) in terms of the quality of single rescuer pediatric resuscitation. Therefore, our hypothesis was that there would be no difference between both CPR methods in terms of chest compression quality parameters.

Read the detailed 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.

02

Conditions studied

  • Cardiac Arrest

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03

In context

Heart Arrest

966 studies on the registry are indexed under Heart Arrest; 227 are open to participants now.

This study's enrollment of 132 is above the median of 100 across 557 interventional studies indexed under Heart Arrest.

Browse Heart Arrest studies →

Lead sponsor

International Institute of Rescue Research and Education is the lead sponsor of 36 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • give voluntary consent to participate in the study
  • medical profession (paramedics, nurses, physicians) or medical students (nurses, paramedics, physicians)

Exclusion criteria

Exclusion Criteria:

  • not meet the above criteria
  • wrist or low back diseases
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
132 participants (actual)

Study arms

  • Experimental
    Chest compression of manikins chest

    Compression of pediatric manikins chest according European Resuscitation Council 2010 guidelines for cardiopulmonary resuscitation.

    Device: The TrueCPR feedback device · Device: Standard BLS

Interventions

  • DeviceThe TrueCPR feedback device

    feedback devices

  • DeviceStandard BLS

    Standard basic life support = chest compressions without any feedback device (manual resuscitation)

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What researchers measure

Primary outcomes

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

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

    Time frame: 1 month

Secondary outcomes

  1. effective compressions ratio effective compressions [%] multiplied by flow time [%]

    effective compressions ratio was defined as effective compressions \[%\] multiplied by flow time \[%\]

    Time frame: 1 month

  2. Flow time sum of all periods during which chest compressions were performed.

    flow time was defined as the sum of all periods during which chest compressions were performed.

    Time frame: 1 month

  3. absolute hands-off time sum of all periods without chest compressions or ventilation

    absolute hands-off time (HOT) was defined as the sum of all periods without chest compressions or ventilation

    Time frame: 1 month

  4. Compression depth compression in correct depth (40-50mm) measured by the software is connected to the manikin and computer

    compression in correct depth (40-50mm) measured by the software is connected to the manikin and computer

    Time frame: 1 month

07

Study locations

1 site
  • International Institute of Rescue Research and Education
    Warsaw, Masovia 03-122, Poland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 18, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02281903
Lead sponsor
International Institute of Rescue Research and Education
Responsible party
Lukasz Szarpak (Lukasz Szarpak, National Institute of Cardiology, Warsaw, Poland) — Principal investigator
First posted
Nov 4, 2014
Start date
Oct 2014
Primary completion
Nov 2014
Completion
Nov 2014
Last update
Nov 18, 2014

Study contacts

Lukasz Szarpak
principal investigator · Institute of Cardiology

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2014. You cannot join it, but the record below documents what was studied.

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