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CPR Feedback Devices

Primary Purpose

Cardiac Arrest

Status
Unknown status
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Standard BLS
TrueCPR
Sponsored by
International Institute of Rescue Research and Education
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Arrest

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Give voluntary consent to participate in the study

Exclusion Criteria:

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

Sites / Locations

  • International Institute of Rescue Research and EducationRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Traditional learning

Experimental learning

Arm Description

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

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.

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

effective compressions ratio effective compressions [%] multiplied by flow time [%]
effective compressions ratio was defined as effective compressions [%] multiplied by flow time [%]
Flow time sum of all periods during which chest compressions were performed.
flow time was defined as the sum of all periods during which chest compressions were performed.
absolute hands-off time sum of all periods without chest compressions or ventilation
absolute hands-off time (HOT) was defined as the sum of all periods without chest compressions or ventilation
Compression depth compression in correct depth (40-50mm) measured by the software is connected to the manikin and computer
compression in correct depth (40-50mm) measured by the software is connected to the manikin and computer

Full Information

First Posted
November 13, 2014
Last Updated
November 17, 2014
Sponsor
International Institute of Rescue Research and Education
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1. Study Identification

Unique Protocol Identification Number
NCT02293200
Brief Title
CPR Feedback Devices
Official Title
TWO METHODS OF TRAINING TO IMPROVE CHEST COMPRESSION EFFECITVENESS BY MEDICAL STUDENTS AND BYSTANDERS: A Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Unknown status
Study Start Date
November 2014 (undefined)
Primary Completion Date
December 2014 (Anticipated)
Study Completion Date
December 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
International Institute of Rescue Research and Education

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Arrest

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Traditional learning
Arm Type
Experimental
Arm Description
chest compression group learning without CPR feedback device. After a month of quality control of chest compressions is made also without the device.
Arm Title
Experimental learning
Arm Type
Experimental
Arm 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.
Intervention Type
Device
Intervention Name(s)
Standard BLS
Intervention Description
basic life support without any feedback device
Intervention Type
Device
Intervention Name(s)
TrueCPR
Intervention Description
CPR with feedback device
Primary Outcome Measure Information:
Title
Effective compressions compression with correct depth (40-50mm), correct hand position and complete decompressions
Description
effective compressions was defined as compression with correct depth (40-50mm), correct hand position and complete decompressions
Time Frame
1 month
Secondary Outcome Measure Information:
Title
effective compressions ratio effective compressions [%] multiplied by flow time [%]
Description
effective compressions ratio was defined as effective compressions [%] multiplied by flow time [%]
Time Frame
1 month
Title
Flow time sum of all periods during which chest compressions were performed.
Description
flow time was defined as the sum of all periods during which chest compressions were performed.
Time Frame
1 month
Title
absolute hands-off time sum of all periods without chest compressions or ventilation
Description
absolute hands-off time (HOT) was defined as the sum of all periods without chest compressions or ventilation
Time Frame
1 month
Title
Compression depth compression in correct depth (40-50mm) measured by the software is connected to the manikin and computer
Description
compression in correct depth (40-50mm) measured by the software is connected to the manikin and computer
Time Frame
1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Give voluntary consent to participate in the study Exclusion Criteria: Not meet the above criteria Wrist or low back diseases
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Andrzej Kurowski
Phone
+48500186225
Email
andrzejkurowski987@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lukasz Szarpak
Organizational Affiliation
Institute of Cardiology
Official's Role
Principal Investigator
Facility Information:
Facility Name
International Institute of Rescue Research and Education
City
Warsaw
State/Province
Masovia
ZIP/Postal Code
03-122
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lukasz Szarpak
Phone
+48500186225
Email
lukasz.szarpak@gmail.com

12. IPD Sharing Statement

Learn more about this trial

CPR Feedback Devices

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