NOT_YET_RECRUITING

Gathering Evidence on Best Practices for Lay Rescuer CPR Training

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 prospective trial is to compare CPR skill and attitudes in lay rescuers. The main question\[s\] it aims to answer are: * What is the optimal training timing, duration, and frequency for lay rescuers that leads to CPR skill retention? * What is the impact of CPR manikin type (high-fidelity, inflatable, nontraditional objects) on skill retention? * How do specific features of training modality -- such as contextualization, gamification, and emotional engagement -- impact skill proficiency, knowledge retention, and attitudes about CPR? Participants will * Answer pre-training questionnaires * Participate in CPR training * Participate in CPR skills testing * Answer post-training questionnaires Researchers will compare different methods of training, different frequencies of training, and different manikin types.

Official Title

Generating Evidence to Optimize Lay Rescuer Cardiopulmonary Resuscitation (CPR) Training: a Longitudinal Study of Frequency, Modality, and Design Features Impacting Skill Retention

Quick Facts

Study Start:2026-04-01
Study Completion:2031-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:NOT_YET_RECRUITING

Study ID

NCT05908500

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:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * All students at participating schools
  1. * Previous CPR training (will be included in the CPR training but excluded from analysis)
  2. * Physical injury which prevents performing CPR
  3. * Student or parent opt-out

Contacts and Locations

Study Contact

Lorrel Toft, MD
CONTACT
4103028456
ltoft@unr.edu

Principal Investigator

Lorrel Toft
PRINCIPAL_INVESTIGATOR
University of Nevada, Reno

Study Locations (Sites)

University of Nevada Reno
Reno, Nevada, 89557
United States

Collaborators and Investigators

Sponsor: University of Nevada, Reno

  • Lorrel Toft, PRINCIPAL_INVESTIGATOR, University of Nevada, Reno

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 Date2026-04-01
Study Completion Date2031-03-31

Study Record Updates

Study Start Date2026-04-01
Study Completion Date2031-03-31

Terms related to this study

Keywords Provided by Researchers

  • Cardiopulmonary Resuscitation
  • cardiopulmonary resuscitation training
  • Lay Rescuer cardiopulmonary resuscitation
  • lay rescuer cardiopulmonary resuscitation training

Additional Relevant MeSH Terms

  • Cardiac Arrest, Out-Of-Hospital