CPR_NURSE: Pediatric Resuscitation With Feedback Devices

Sponsor
International Institute of Rescue Research and Education (Other)
Overall Status
Unknown status
CT.gov ID
NCT02294721
Collaborator
(none)
200
1
2
30
202.9

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Standard BLS
  • Device: The CPREazy
  • Device: TrueCPR
  • Device: The CPR PRO APP
  • Device: The CardioPump
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Quality of Pediatric Chest Compression: Comparing Four CPR Feedback Devices With Standard BLS by a Single Rescuer: A Randomised Controlled Manikin Trial
Study Start Date :
Nov 1, 2014
Anticipated Primary Completion Date :
Dec 1, 2014
Anticipated Study Completion Date :
Dec 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Without feedback

Participants compress the chest of the manikin without CPR feedback device

Device: Standard BLS
Resuscitation without feedback devices, standard manual standard basic life support

Experimental: With feedback

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

Device: The CPREazy
feedback device-1

Device: TrueCPR
feedback device -2

Device: The CPR PRO APP
feedback device -3

Device: The CardioPump
feedback device- 4

Outcome Measures

Primary Outcome Measures

  1. Effective compressions [1 day]

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

Secondary Outcome Measures

  1. Chest compression depth [1 day]

    To measure chest compression depth during 8 minutes. Chest compression depth will be measured using the software connected to the manikin and computer

  2. Chest compression rate [1 day]

    To measure the chest compression rate during 8 minutes. Chest compression rate will be measured using the software connected to the manikin and computer

  3. effective compressions ratio [1day]

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

  4. Flow time was defined as the sum of all periods during which chest compressions were performed [1 day]

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

  5. absolute hands-off time [1 day]

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

  6. VAS (visual analogue scale) [1 day]

    after 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)

  7. Prefered CPR device [1 day]

    after 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)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 International Institute of Rescue Research and Education Warsaw Masovia Poland 03-122

Sponsors and Collaborators

  • International Institute of Rescue Research and Education

Investigators

  • Principal Investigator: Lukasz Szarpak, Institute of Cardiology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lukasz Szarpak, Lukasz Szarpak, Institute of Cardiology, Warsaw, Poland
ClinicalTrials.gov Identifier:
NCT02294721
Other Study ID Numbers:
  • CPR/2014/10
First Posted:
Nov 19, 2014
Last Update Posted:
Nov 19, 2014
Last Verified:
Nov 1, 2014
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 19, 2014