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Pediatric Resuscitation With Feedback Devices

NCT ID: NCT02294721

Last Updated: 2014-11-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-11-30

Study Completion Date

2014-12-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Cardiac Arrest

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Without feedback

Participants compress the chest of the manikin without CPR feedback device

Group Type EXPERIMENTAL

Standard BLS

Intervention Type DEVICE

Resuscitation without feedback devices, standard manual standard basic life support

With feedback

Participants compress the chest of the manikin with CPR feedback device.

Group Type EXPERIMENTAL

The CPREazy

Intervention Type DEVICE

feedback device-1

TrueCPR

Intervention Type DEVICE

feedback device -2

The CPR PRO APP

Intervention Type DEVICE

feedback device -3

The CardioPump

Intervention Type DEVICE

feedback device- 4

Interventions

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Standard BLS

Resuscitation without feedback devices, standard manual standard basic life support

Intervention Type DEVICE

The CPREazy

feedback device-1

Intervention Type DEVICE

TrueCPR

feedback device -2

Intervention Type DEVICE

The CPR PRO APP

feedback device -3

Intervention Type DEVICE

The CardioPump

feedback device- 4

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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International Institute of Rescue Research and Education

OTHER

Sponsor Role lead

Responsible Party

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Lukasz Szarpak

Lukasz Szarpak

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Lukasz Szarpak

Role: PRINCIPAL_INVESTIGATOR

Institute of Cardiology

Locations

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International Institute of Rescue Research and Education

Warsaw, Masovia, Poland

Site Status RECRUITING

Countries

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Poland

Central Contacts

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Andrzej Kurowski

Role: CONTACT

[email protected]
+48500186225

Other Identifiers

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CPR/2014/10

Identifier Type: -

Identifier Source: org_study_id