Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
Healthy Volunteers
ID05868239

Impact of Aerosol Box Use During Cardiopulmonary Arrest: A Multicenter Study

Led by KidSIM Simulation Program · Updated on 2025-09-05

240

Participants Needed

4

Research Sites

65 weeks

Total Duration

On this page

Sponsors

K

KidSIM Simulation Program

Lead Sponsor

C

Canadian Institutes of Health Research (CIHR)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The study focuses on protecting healthcare workers (HCWs) from infection risks during aerosol-generating medical procedures (AGMPs) performed on critically ill COVID-19 patients. These procedures include bag-valve-mask ventilation, endotracheal intubation, and cardiopulmonary resuscitation (CPR), which can release virus-containing particles into the air. The research aims to evaluate the effectiveness of an aerosol box, a transparent barrier placed over the patient's head, in reducing contamination of HCWs during resuscitation while observing its impact on clinical task performance. Participants will be organized into teams including airway providers and CPR providers, who will perform simulated cardiac arrest scenarios either using the aerosol box device or without it. Teams will be trained and randomized to either the intervention group with aerosol box use or the control group without the box. The study includes video-based orientation, practice sessions, and randomized scenario order to assess the effect on CPR quality, intubation timing, airborne particle counts, and contamination. During the study, researchers will monitor team performance with multiple measurements including overall CPR quality, intubation success time, chest compression fraction, particle concentration near the patient, provider contamination area, and provider workload and anxiety. Data will be collected immediately after simulations, and participants will receive debriefing on performance and infection control. The study is designed to improve safety protocols for HCWs during pandemics by providing evidence about aerosol box use in a controlled simulated environment.

CONDITIONS

Brief Title

Impact of Aerosol Box Use During Cardiopulmonary Arrest: A Multicenter Study

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Attending physician, fellow, or resident in adult or pediatric emergency medicine, pediatric intensive care, general pediatrics, or pediatric/adult anesthesia
  • Adult or Pediatric Advanced Life Support certification
  • Attending physician, resident, fellow, nurse, respiratory therapist, physician assistant, or health care aide
  • Basic Life Support, Adult or Pediatric Advanced Life Support certification
Not Eligible

You will not qualify if you...

  • Decline to provide informed consent
  • Unable to perform tasks required of the role due to physical limitations

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit

Implementation

Duration - Single session lasting approximately 1 to 2 hours

Participants work in teams to practice and perform simulated cardiopulmonary resuscitation scenarios with or without use of an aerosol box in a controlled simulation environment.

1 in-person visit including orientation, training, simulation scenarios, and debriefing

Trial Site Locations

Total: 4 locations

1

Department of Emergency Medicine, Children's Hospital of Los Angeles

Los Angeles, California, United States, 90027

Actively Recruiting

2

KidSIM, Alberta Children's Hospital

Calgary, Alberta, Canada, T3B6A8

Actively Recruiting

3

Department of Pediatrics, The Hospital for Sick Children

Toronto, Ontario, Canada

Actively Recruiting

4

Department of Pediatrics, CHU Sainte-Justine

Montreal, Quebec, Canada

Completed

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Research Team

A

Adam Cheng, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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