- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02293200
CPR Feedback Devices
November 17, 2014 updated by: Lukasz Szarpak, International Institute of Rescue Research and Education
TWO METHODS OF TRAINING TO IMPROVE CHEST COMPRESSION EFFECITVENESS BY MEDICAL STUDENTS AND BYSTANDERS: A Randomized Trial
The aim of the study was to compare two methods of training in CPR, standard basic life support and CPR using CPR feedback device.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
200
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Masovia
-
Warsaw, Masovia, Poland, 03-122
- Recruiting
- International Institute of Rescue Research and Education
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Give voluntary consent to participate in the study
Exclusion Criteria:
- Not meet the above criteria
- Wrist or low back diseases
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Traditional learning
chest compression group learning without CPR feedback device.
After a month of quality control of chest compressions is made also without the device.
|
basic life support without any feedback device
|
EXPERIMENTAL: Experimental learning
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.
|
basic life support without any feedback device
CPR with feedback device
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Effective compressions compression with correct depth (40-50mm), correct hand position and complete decompressions
Time Frame: 1 month
|
effective compressions was defined as compression with correct depth (40-50mm), correct hand position and complete decompressions
|
1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
effective compressions ratio effective compressions [%] multiplied by flow time [%]
Time Frame: 1 month
|
effective compressions ratio was defined as effective compressions [%] multiplied by flow time [%]
|
1 month
|
Flow time sum of all periods during which chest compressions were performed.
Time Frame: 1 month
|
flow time was defined as the sum of all periods during which chest compressions were performed.
|
1 month
|
absolute hands-off time sum of all periods without chest compressions or ventilation
Time Frame: 1 month
|
absolute hands-off time (HOT) was defined as the sum of all periods without chest compressions or ventilation
|
1 month
|
Compression depth compression in correct depth (40-50mm) measured by the software is connected to the manikin and computer
Time Frame: 1 month
|
compression in correct depth (40-50mm) measured by the software is connected to the manikin and computer
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2014
Primary Completion (ANTICIPATED)
December 1, 2014
Study Completion (ANTICIPATED)
December 1, 2014
Study Registration Dates
First Submitted
November 13, 2014
First Submitted That Met QC Criteria
November 17, 2014
First Posted (ESTIMATE)
November 18, 2014
Study Record Updates
Last Update Posted (ESTIMATE)
November 18, 2014
Last Update Submitted That Met QC Criteria
November 17, 2014
Last Verified
November 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CPR/2014/03
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Cardiac Arrest
-
Australian and New Zealand Intensive Care Research...Ambulance VictoriaNot yet recruitingOut of Hospital Cardiac Arrest
-
University Medical Centre MariborRecruiting
-
IRCCS Policlinico S. MatteoOslo University Hospital; University of the Basque Country (UPV/EHU); The Hospital...CompletedOut-Of-Hospital Cardiac ArrestItaly, Norway, Spain
-
Lithuanian University of Health SciencesEgle Vaitkaitiene; Dinas Vaitkaitis; Asta Krikscionaitiene; Ilona Kajokaite; Nerijus...CompletedOut-Of-Hospital Cardiac ArrestLithuania
-
Ceric SàrlAbbottTerminatedOut of Hospital Cardiac ArrestBelgium, France, Serbia
-
Prehospital Center, Region ZealandCompletedOut-Of-Hospital Cardiac Arrest
-
Karolinska InstitutetSwedish Heart Lung FoundationCompletedCardiac Arrest | Out of Hospital Cardiac ArrestSweden
-
Karolinska InstitutetVastra Gotaland Region; SOS Alarm Sverige AB; Everdrone AB; Aviation capacity resources... and other collaboratorsCompleted
-
Brno University HospitalTerminatedOut-Of-Hospital Cardiac ArrestCzechia
-
SRINIVAS RAMAKAUnknownOut-Of-Hospital Cardiac ArrestIndia
Clinical Trials on Standard BLS
-
Ottawa Hospital Research InstituteCompletedCardiopulmonary Resuscitation | Basic Life Saving Skills | Skill RetentionCanada
-
International Institute of Rescue Research and...Completed
-
International Institute of Rescue Research and...Unknown
-
Copenhagen Academy for Medical Education and SimulationUniversity of Southern Denmark; TrygFonden, Denmark; Emergency Medical Services...CompletedCardiopulmonary Resuscitation | Basic Cardiac Life SupportDenmark
-
University Hospital Inselspital, BerneCompleted
-
International Institute of Rescue Research and...Unknown
-
BioLeaders CorporationCompleted
-
yousef Shukry Mohammad Abu-WardehActive, not recruitingEducational Activities | Healthy NursesJordan
-
Chang Gung University of Science and TechnologyCompletedCommunity DwellingTaiwan
-
University of BirminghamHeart of England NHS Trust; Calderdale and Huddersfield NHS Foundation Trust; Resuscitation Council UKCompletedCardiac Arrest