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Effectiveness of Pediatric Resuscitation

Quality of Chest Compressions During 8 Min of Single-rescuer Pediatric Cardiopulmonary Resuscitation With Five Different CPR Feedback Devices. Randomised Crossover Manikin Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02283034
Acronym
EPR
Enrollment
120
Registered
2014-11-05
Start date
2014-10-31
Completion date
2014-11-30
Last updated
2014-11-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest

Brief summary

The aim of this study was to compare five 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.

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.

Interventions

DEVICEThe CPRmeter

Feedback device - 1

DEVICEThe PocketCPR

Feedback device - 2

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

Feedback device - 3

Feedback device - 4

Feedback devices - 5

Sponsors

International Institute of Rescue Research and Education
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
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

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

Design outcomes

Primary

MeasureTime frameDescription
Effective compressions was defined as compression with correct depth (40-50mm), correct hand position and complete decompressions1 montheffective compressions was defined as compression with correct depth (40-50mm), correct hand position and complete decompressions

Secondary

MeasureTime frameDescription
Chest compression rate1 monthTo measure the chest compression rate during 8 minutes. Chest compression rate will be measured using the software connected to the manikin and computer
effective compressions ratio was defined as effective compressions [%] multiplied by flow time [%]1 montheffective compressions ratio was defined as effective compressions \[%\] multiplied by flow time \[%\]
Flow time was defined as the sum of all periods during which chest compressions were performed1 monthflow time was defined as the sum of all periods during which chest compressions were performed.
Chest compression depth1 monthTo measure chest compression depth during 8 minutes. Chest compression depth will be measured using the software connected to the manikin and computer
VAS (visual analogue scale)1 monthafter having completed the 8 min testing period, the study participants were asked how challenging they had experienced standard BLS or resuscitation which the respective feedback device. answers were rated on a 10-point Lickert scale (most difficult = 1 to easiest = 10)
Prefered CPR device1 monthafter having completed the 8 min testing period, the study participants were asked how chellenging whitch method they would preferred. answers were rated on a 10-point Lickert scale (lower preferred = 1 to most preferred = 10)
absolute hands-off time was defined as the sum of all periods without chest compressions or ventilation1 monthabsolute hands-off time (HOT) was defined as the sum of all periods without chest compressions or ventilation

Countries

Poland

Contacts

Primary ContactLukasz Szarpak
lukasz.szarpak@gmail.com+48500186225

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026