About this trial
Cognitive aids are decision support tools that present prompts to encourage recall of information, thus freeing up mental resources to increase the likelihood of desired behaviors. Cognitive aids have been trialed in different forms for use during resuscitation, including pocket reference cards and digital apps. Simulation-based studies of cognitive aid used during cardiac arrest events have shown improved adherence to guidelines, improved time to completing critical tasks, and reduced rate of critical errors. Unfortunately, existing pocket reference cards and mobile apps have significant flaws - they all require providers to search through content to identify relevant information.
In the proposed study, the investigators will evaluate the impact of an enhanced system, InterFACE-AR, which provides role-specific decision support to the team leader and medication nurse through AR devices, while concurrently optimizing team situational awareness by displaying a roadmap for patient care on the LCD screen. Clinical data will be collected from the mobile app on a tablet used by the charting nurse. The trial aims to assess the individual and combined effectiveness of InterFACE-AR components (i.e. AR devices and LCD screen) on adherence to AHA resuscitation guidelines during simulated cardiac arrest by conducting a randomized controlled trial with a factorial design.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
Decline to provide informed consent
previously enrolled
unable to perform tasks required of the role.
Trial design
Factorial
Treatments tested in this trial
Augmented reality
DeviceAugmented Reality Devices - data collected from the Guiding-Pad app will be fed to two AR devices (i.e. team leader and medication nurse), which will provide role-specific decision support for these two providers.
LCD Screen
DeviceLCD Screen - data collected from the Guiding-Pad app will be fed to the LCD screen, which will be mounted on a wall, in clear view for the entire resuscitation team to see.
Treatment groups
Trial outcomes
Primary outcomes
Time to epinephrine
Time to epinephrine administration, in seconds
Secondary outcomes
Time to initiation of CPR
Time to initiation of CPR, in seconds
Time to defibrillation
Time to defibrillation, in seconds
Time to amiodarone administration
Time to amiodarone administration, in seconds
Time to intubation
Time to intubation, in seconds
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
KidSIM Simulation Program
Lead sponsor
University of Calgary
Sponsor institution
Laval University
Collaborator
University of Toronto
Collaborator
University of Padova
Collaborator
University of Alabama at Birmingham
Collaborator
University of Southern California
Collaborator
Columbia University
Collaborator
University of Genova
Collaborator
University of Calgary
Collaborator
This trial is not recruiting at the moment. You can still explore other options: