CPR Feedback Devices

International Institute of Rescue Research and Education

Status: Unknown

Conditions: Cardiac Arrest

Treatments: Device: Standard BLS; Device: TrueCPR

Study type: Interventional

Funder types: Other

Identifiers

NCT02293200

CPR/2014/03

Details and patient eligibility

About

The aim of the study was to compare two methods of training in CPR, standard basic life support and CPR using CPR feedback device.

Enrollment: 200 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Give voluntary consent to participate in the study

Exclusion criteria

• Not meet the above criteria
• Wrist or low back diseases

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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200 participants in 2 patient groups

Traditional learning

Experimental group

Description:

chest compression group learning without CPR feedback device. After a month of quality control of chest compressions is made also without the device.

Treatment:

Device: Standard BLS

Experimental learning

Experimental group

Description:

Training is done using TrueCPR feedback device. After a month of quality control of chest compressions is made without the device. To do this will be indicated on the impact of the use of feedback devices for improving the effectiveness of training in CPR.

Treatment:

Device: TrueCPR

Device: Standard BLS