Evaluation of the InterFACE-AR System for Cardiopulmonary Arrest

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKidSIM Simulation Program

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 volunteers

Qualifiers

None

Disqualifiers

Decline to provide informed consent

previously enrolled

unable to perform tasks required of the role.

Trial design

Design model

Factorial

Treatments tested in this trial

  • Augmented reality

    Device

    Augmented 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

    Device

    LCD 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

400 Participants
are divided into 4 treatment groups
Group A: Control ArmNo intervention 0 interventions
Group B: Augmented Reality OnlyExperimental treatment 1 intervention
Group C: LCD Screen OnlyExperimental treatment 1 intervention
Group D: Augmented Reality + LCD Screen (Full InterFACE-AR System)Experimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Time to epinephrine

Time to epinephrine administration, in seconds

Time frame
During event

Secondary outcomes

1

Time to initiation of CPR

Time to initiation of CPR, in seconds

Time frame
During event
2

Time to defibrillation

Time to defibrillation, in seconds

Time frame
During event
3

Time to amiodarone administration

Time to amiodarone administration, in seconds

Time frame
During event
4

Time to intubation

Time to intubation, in seconds

Time frame
During event

Other outcomes

Locations

This trial has no 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: