RESCUER mobile app to support pediatric resuscitation: Study protocol for a randomized controlled trial.
Samantha A Lee, Diego Trujillo, Garth D Meckler...
https://pubmed.ncbi.nlm.nih.gov/41142041Actively Recruiting
Led by Beth Israel Deaconess Medical Center · Updated on 2026-04-13
80
Participants Needed
2
Research Sites
52 weeks
Total Duration
B
Beth Israel Deaconess Medical Center
Lead Sponsor
N
National Heart, Lung, and Blood Institute (NHLBI)
Collaborating Sponsor
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
A Clinical Trial to Study the Feasibility and Acceptability of an App to Support Pediatric Resuscitation
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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)
Total: 2 locations
1
20 Overland 4th floor
Boston, Massachusetts, United States, 02215
Actively Recruiting
2
BIDMC
Boston, Massachusetts, United States, 02215
Actively Recruiting
J
Jeanne-Marie Guise, MD, MPH, MBA
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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Samantha A Lee, Diego Trujillo, Garth D Meckler...
https://pubmed.ncbi.nlm.nih.gov/41142041