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Completed

NCT Number: NCT02142387

Effects of a New Dispatcher-Assisted Basic Life Support Training Program

Despite aggressive cardiopulmonary resuscitation (CPR) training, the outcome of cardiac arrest is not good. The problem is method of education. So, the investigators want to add the dispatcher-assisted CPR simulation into conventional CPR training. In this study, the study is aimed to investigate the effect of newer CPR training program.

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Seoul National University Hospital

Seoul, 110-744, South Korea

About this study

The training program focuses on working in team with dispatcher, performing all steps from recognizing cardiac arrest to performing CPR, together with the dispatcher. The one hours training session is split into four parts:

  • Video self-instruction manikin practice (30 min), including a brief introduction to automated external defibrillator (AED).
  • Practice in pairs (15 min). Practicing the dispatcher and rescuer role in a simulation to enhance learning.
  • Debriefing. Questions, answers and reflection (15 min).
  • Homework. Leaflet with tasks like learn how to activate the speaker function on your own phone.

The main difference between dispatcher-assisted basic life support (DA-BLS) and traditional BLS training is that DA-BLS provides the scenes and interactive experiences on calling emergency medical service (EMS) and receiving CPR instruction via telephone speaker function, following up the skill training by scenario simulation training.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All out-of-hospital cardiac arrest (OHCA) patients with presumed cardiac etiology who are 19 years of age or older and assessed and treated by EMS providers after dispatched by the EMS dispatch center will be included.

Exclusion criteria

  • We will exclude patients with non-cardiac etiology, prolonged cardiac arrest with a suspected duration more than 30 minutes, cases such as livor mortis or rigor mortis, and decapitated or decomposed body, and patients who have "Do-Not-Resuscitate" card documented by doctor.

Treatment and study plan

BLS CPR program with dispatcher assisted CPR simulation

Other

the training program more focuses on cooperation with a dispatcher, from recognition to perform DA-CPR and hands-on practice.

Primary outcomes

  1. Number of Participants Surviving to Hospital Discharge

    Time frame: from date of discharge, assessed up to 3 months

    The study end points are survival to hospital discharge. Survival to discharge will be measured as proportions of patients who were discharged from a hospital with their spontaneous circulation recovered. This information will be collected from medical record review.

Secondary outcomes

  1. Number of Participants With Return of Spontaneous Circulation (ROSC)

    Time frame: from date of cardiac arrest occurred, assessed up to 1 week

    The return of spontaneous circulation will be measured as proportion of the patients who were recovered their circulation at emergency department. This information will be collected from the medical review.

  2. Number of Participants With Good Neurological Recovery

    Time frame: from date of discharge, assessed up to 3 months

    The Cerebral Performance Categories (CPC) score will be used to measure neurological recovery status: CPC 1 (good cerebral performance), CPC 2 (moderate cerebral disability), CPC 3 (severe cerebral disability), CPC 4 (coma or vegetative state), CPC 5 (brain death).

    We defined the good neurological recovery as CPC 1 or CPC 2. This information will be collected from medical record review.

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Registry information

Official study title

Clinical Effects of a New Dispatcher-Assisted Basic Life Support Training Program in a Metropolitan City: A Before-and-After Intervention Study

Acronym: HEROS

Important dates

Study start
2014
Primary completion
2017
Study completion
2018
First posted
May 20, 2014
Registry last updated
May 1, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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