Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID06768099

Reducing Disparities for Children in Rural Emergency Resuscitation: Testing an Integrated Linear Cognitive Aid for Pediatric Resuscitation

Led by Beth Israel Deaconess Medical Center · Updated on 2026-04-13

80

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

Sponsors

B

Beth Israel Deaconess Medical Center

Lead Sponsor

N

National Heart, Lung, and Blood Institute (NHLBI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This clinical trial studies the use of a linear cognitive aid app designed to help emergency medical service (EMS) teams respond to pediatric emergencies. Researchers want to see if this new tool is practical and well accepted by EMS teams in both urban and rural settings. The study compares current standard cognitive aids with the new linear cognitive aid during simulated critical resuscitation scenarios for children. Participants will be randomized into two groups: one using their current standard cognitive aids, and the other using the linear cognitive aid app. Each team will perform two high-fidelity, in situ simulations of critical pediatric resuscitation emergencies. The linear cognitive aid app offers minimal input, linear step-by-step guidance, tailored recommendations based on the patient’s age and scenario, and audio prompts timed to the resuscitation process. During the study, researchers will assess the time it takes teams to reach American Heart Association (AHA) technical milestones, teamwork quality, and participants' perceived cognitive load during each 10-minute simulation. The study aims to evaluate how well teams perform and how the different cognitive aids affect their experience. The trial is led by Beth Israel Deaconess Medical Center and includes adult EMS providers who speak English and are actively practicing.

CONDITIONS

Brief Title

A Clinical Trial to Study the Feasibility and Acceptability of an App to Support Pediatric Resuscitation

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Active public, private, volunteer, hospital-based, or third-party EMS providers
  • Speaks and understands English
  • Age 18 and over
Not Eligible

You will not qualify if you...

  • Not clinically active

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 visit (in-person)

Simulation Sessions

Duration - Single session per participant

Participants engage in high-fidelity simulations of pediatric emergency resuscitation scenarios using either the current standard cognitive aids or the linear cognitive aid app.

1 visit (in-person)

Trial Site Locations

Total: 2 locations

1

20 Overland 4th floor

Boston, Massachusetts, United States, 02215

Actively Recruiting

2

BIDMC

Boston, Massachusetts, United States, 02215

Actively Recruiting

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Research Team

J

Jeanne-Marie Guise, MD, MPH, MBA

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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Published Research Related To This Trial