RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinicial trial is to test the acceptability and feasibility of linear cognitive aid intervention to support EMS teams in responding to pediatric emergencies. We are testing the hypothesis that cognitive aids with linear logic will be feasible to use and acceptable to EMS teams in urban and rural areas. Researchers will compare technical performance, teamwork, and self-assessed cognitive load of participants to see the difference between performing resuscitations using their current standard with existing cognitive aids and using our linear cognitive aid. Participants' teams will: * perform in situ high-fidelity simulation of two critical children's resuscitation scenarios * be randomized to 1) perform both resuscitations with their current standard with existing cognitive aids or 2) perform both resuscitations using our linear cognitive aid.

Official Title

Reducing Disparities for Children in Rural Emergency Resuscitation (RESCU-ER): Developing and Testing the Acceptability and Feasibility of an Integrated Linear Cognitive Aid for Pediatric Resuscitation in a Pilot RCT

Quick Facts

Study Start:2025-02-18
Study Completion:2026-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06768099

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Active public, private, volunteer, hospital-based, or third-party EMS providers
  2. * Speaks and understands English
  3. * Age 18 and over
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Jeanne-Marie Guise, MD, MPH, MBA
CONTACT
617-667-4130
jguise@bidmc.harvard.edu

Study Locations (Sites)

20 Overland 4th floor
Boston, Massachusetts, 02215
United States
BIDMC
Boston, Massachusetts, 02215
United States

Collaborators and Investigators

Sponsor: Beth Israel Deaconess Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-02-18
Study Completion Date2026-03

Study Record Updates

Study Start Date2025-02-18
Study Completion Date2026-03

Terms related to this study

Keywords Provided by Researchers

  • Pediatric emergency medical services
  • Rural-urban health disparities
  • Child mortality
  • Adverse safety events (ASEs)
  • Prehospital pediatric care
  • Cognitive aid
  • Randomized controlled trial (RCT)
  • Emergency resuscitation
  • Out of hospital Cardiac arrest

Additional Relevant MeSH Terms

  • Pediatric Emergency Medicine
  • Resuscitation
  • Pediatrics
  • Emergency Medical Services
  • Arrest Cardio Respiratory