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Clinical Trials/NCT03690102
NCT03690102CompletedNot Applicable

The Effect of Telephone Assistance on the Quality of Cardiopulmonary Resuscitation and Use of Automated External Defibrillator.

Copenhagen Academy for Medical Education and Simulation2 sites in 1 country153 target enrollmentStarted: September 30, 2018Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
153
Locations
2
Primary Endpoint
Compression rate

Study Overview

Brief Summary

The purpose of the study is to examine the effect of telephone assistance and standardized basic life support courses on the quality of cardiopulmonary resuscitation (CPR) and the use of automated external defibrillator (AED).

The investigators hypothesize that bystanders can provide compressions in correct frequency and use an AED correctly as well as safely from telephone instructions but that correct and successful ventilations including correct open airway require training on a course.

Detailed Description

The study aims at answering the following research questions:

  1. How is the quality of CPR and use of AED when performed by an inexperienced bystander who receives telephone assistance compared to the quality when performed by a trained bystander, who has passed a standardized European Resuscitation Council (ERC) course in basic life support (BLS) but does not receive telephone assistance?
  2. How is the quality of CPR and use of AED when performed by a trained bystander who has passed a standardized ERC course in BLS and who receives telephone assistance compared to the quality when performed by a trained bystander who does not receive telephone assistance?

The questions are sought answered through simulated cardiac arrest scenarios in non-classroom settings.

Participants are recruited from ERC courses in BLS.

Participants are randomised to one of three groups (stratified for course type using computer-generated randomisation lists with blocks of variable sizes):

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Participant at a European Resuscitation Council standardized basic life support course. Participants are enrolled from courses for university students, courses for elderly and courses for recruits in the Danish Emergency Management Agency.

Exclusion Criteria

  • Basic life support course within the last two years.
  • Healthcare professional or background as healthcare professional.
  • Instructor in basic life support or first aid.
  • Lifeguard or background as lifeguard.
  • Does not want to participate.

Outcomes

Primary Outcomes

Compression rate

Time Frame: 8 minutes

Rescuer keeps a compression rate of approximately 100-120 compressions per min. throughout the CPR (yes/no). Measured by advanced manikin.

Shock delivered

Time Frame: 8 minutes

Shock delivered with AED (yes/no). Assessed by ERC instructor.

Compression depth

Time Frame: 8 minutes

Keeps a compression depth as recommended by International Liaison Committee on Resuscitation (ILCOR) (5-6 cm) on at least 50 % of compressions (yes/no). Measured by advanced manikin.

Secondary Outcomes

  • Rescue breaths(8 minutes)
  • Time to first compression(8 minutes)
  • Open airway(8 minutes)
  • Rescue breaths 2(8 minutes)
  • Hands-of time(8 minutes)
  • Assess breathing(8 minutes)
  • Ratio(8 minutes)
  • Attachment of AED pads(8 minutes)
  • Compression depth 2(8 minutes)
  • Recoil/lean(8 minutes)
  • Activate AED(8 minutes)
  • Stand clear(8 minutes)
  • Compression rate 2(8 minutes)
  • Responsiveness(8 minutes)
  • Hand placement(8 minutes)

Investigators

Sponsor
Copenhagen Academy for Medical Education and Simulation
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Kristine Elisabeth Eberhard

Researcher, medical student

Copenhagen Academy for Medical Education and Simulation

Study Sites (2)

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