Study Results
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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UNKNOWN
NA
120 participants
INTERVENTIONAL
2014-10-31
2014-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
SINGLE
Study Groups
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With feedback
Participants compress the chest of the manikin with CPR feedback device.
Standard BLS
Chest compressions without CPR feedback device (manual resuscitation)
Without feedback
Participants compress the chest of the manikin without CPR feedback device
The CPRmeter
Feedback device - 1
The PocketCPR
Feedback device - 2
Standard BLS
Standard basic life support = chest compressions without any feedback device (manual resuscitation)
The CPREazy
Feedback device - 3
The CPR PRO APP
Feedback device - 4
The CardioPump
Feedback devices - 5
Interventions
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The CPRmeter
Feedback device - 1
The PocketCPR
Feedback device - 2
Standard BLS
Standard basic life support = chest compressions without any feedback device (manual resuscitation)
The CPREazy
Feedback device - 3
The CPR PRO APP
Feedback device - 4
The CardioPump
Feedback devices - 5
Standard BLS
Chest compressions without CPR feedback device (manual resuscitation)
Eligibility Criteria
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Inclusion Criteria
* medical profession (paramedics, nurses, physicians) or medical students (nurses, paramedics, physicians)
Exclusion Criteria
* wrist or low back diseases
18 Years
65 Years
ALL
Yes
Sponsors
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International Institute of Rescue Research and Education
OTHER
Responsible Party
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Lukasz Szarpak
Lukasz Szarpak
Principal Investigators
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Andrzej Kurowski
Role: PRINCIPAL_INVESTIGATOR
Institute of Cardiology
Lukasz Szarpak
Role: PRINCIPAL_INVESTIGATOR
Institute of Cardiology
Locations
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International Institute of Rescue Research and Education
Warsaw, Masovia, Poland
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CPR/2014/06
Identifier Type: -
Identifier Source: org_study_id
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