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Combining Performance of Call EMS and Simultaneous Chest Compressions in a Lone Rescuer CPR

Primary Purpose

Out-of-Hospital Cardiac Arrest

Status
Completed
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Combi lone-CPR
Conventional lone-CPR
Sponsored by
Konkuk University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Out-of-Hospital Cardiac Arrest focused on measuring Cardiopulmonary Resuscitation, Emergency Medical Services, Cell phones, Simulation Training

Eligibility Criteria

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

Inclusion Criteria:

  • All healthy volunteers who attended the basic CPR training class
  • Agreement with the simulation trial

Exclusion Criteria:

  • volunteers who had some healthy problem which may affect the study results
  • Not agreement with the simulation trial

Sites / Locations

  • Department of Emergency Medicine, Konkuk University Medical center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Combi lone-CPR

Conventional lone-CPR

Arm Description

Intervention group : Newly developed method

Conventional CPR group

Outcomes

Primary Outcome Measures

Total numbers of chest compression with correct depth
correct depth is defined as depth > 50 mm

Secondary Outcome Measures

Incomplete release of chest compression
Incorrect position of chest compression
Correct Tidal volume
defined as 500-800 ml in manikin setting
Interruption time of chest compression

Full Information

First Posted
December 23, 2015
Last Updated
September 7, 2016
Sponsor
Konkuk University Medical Center
Collaborators
Hallym University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02646046
Brief Title
Combining Performance of Call EMS and Simultaneous Chest Compressions in a Lone Rescuer CPR
Official Title
A Study of Evaluation of Effectiveness on the Combining Performance of Call Emergency Medical System (EMS) and Simultaneous Chest Compressions With One Hand in a Lone Rescuer CPR: a Simulation Study Using the Manikin
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
October 2015 (undefined)
Primary Completion Date
January 2016 (Actual)
Study Completion Date
January 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Konkuk University Medical Center
Collaborators
Hallym University Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Investigators designed the novel combining technique that rescuer start the chest compression with one hand during calling for help to the Emergency Medical System (EMS) via a cell phone with another hand when he witnessed the arrest victim. This method may be helpful to reduce the hand-off time and increase the faction time of chest compression until the arrival of EMS members. To verify this hypothesis, we conducted a random, controlled simulation study.
Detailed Description
This study used a random, controlled design in the simulation setting using a manikin. Study participants were recruited from healthy adult (age > 18 years) laypersons who attended the BLS training courses provided by the BLS training class. The simulation scenario consists of witness of an out of hospital cardiac arrest and activation of the EMS system with the prepared cellular phone. Interventional method contained the immediate starting of the chest compression with one hand during the calling for help to the EMS via a cell phone with another hand. We compare the quality of CPR between the novel interventional method (start CPR during Call to EMS) and conventional method (First Call to EMS and then start CPR).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Out-of-Hospital Cardiac Arrest
Keywords
Cardiopulmonary Resuscitation, Emergency Medical Services, Cell phones, Simulation Training

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
110 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Combi lone-CPR
Arm Type
Experimental
Arm Description
Intervention group : Newly developed method
Arm Title
Conventional lone-CPR
Arm Type
Active Comparator
Arm Description
Conventional CPR group
Intervention Type
Behavioral
Intervention Name(s)
Combi lone-CPR
Intervention Description
When study participants meet the arrest victim (simulated), they start chest compression and call for help to EMS at the same time, then continue the chest compression and 2 breath alternatively until the EMS arrival
Intervention Type
Behavioral
Intervention Name(s)
Conventional lone-CPR
Intervention Description
When study participants meet the arrest victim (simulated), they first call for help to EMS and then start chest compression and 2 breath alternatively until the EMS arrival
Primary Outcome Measure Information:
Title
Total numbers of chest compression with correct depth
Description
correct depth is defined as depth > 50 mm
Time Frame
3 minutes
Secondary Outcome Measure Information:
Title
Incomplete release of chest compression
Time Frame
3 minutes
Title
Incorrect position of chest compression
Time Frame
3 minutes
Title
Correct Tidal volume
Description
defined as 500-800 ml in manikin setting
Time Frame
3 minute
Title
Interruption time of chest compression
Time Frame
3 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: All healthy volunteers who attended the basic CPR training class Agreement with the simulation trial Exclusion Criteria: volunteers who had some healthy problem which may affect the study results Not agreement with the simulation trial
Facility Information:
Facility Name
Department of Emergency Medicine, Konkuk University Medical center
City
Seoul
ZIP/Postal Code
143-729
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
20956051
Citation
Koster RW, Baubin MA, Bossaert LL, Caballero A, Cassan P, Castren M, Granja C, Handley AJ, Monsieurs KG, Perkins GD, Raffay V, Sandroni C. European Resuscitation Council Guidelines for Resuscitation 2010 Section 2. Adult basic life support and use of automated external defibrillators. Resuscitation. 2010 Oct;81(10):1277-92. doi: 10.1016/j.resuscitation.2010.08.009. No abstract available.
Results Reference
background
PubMed Identifier
20956221
Citation
Berg RA, Hemphill R, Abella BS, Aufderheide TP, Cave DM, Hazinski MF, Lerner EB, Rea TD, Sayre MR, Swor RA. Part 5: adult basic life support: 2010 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation. 2010 Nov 2;122(18 Suppl 3):S685-705. doi: 10.1161/CIRCULATIONAHA.110.970939. Erratum In: Circulation. 2011 Oct 11;124(15):e402.
Results Reference
background
PubMed Identifier
17303308
Citation
Riera SQ, Gonzalez BS, Alvarez JT, Fernandez Mdel M, Saura JM. The physiological effect on rescuers of doing 2min of uninterrupted chest compressions. Resuscitation. 2007 Jul;74(1):108-12. doi: 10.1016/j.resuscitation.2006.10.031. Epub 2007 Feb 14.
Results Reference
background

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Combining Performance of Call EMS and Simultaneous Chest Compressions in a Lone Rescuer CPR

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