NCT05908500

Brief Summary

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.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,100

participants targeted

Target at P75+ for not_applicable

Timeline
60mo left

Started Apr 2026

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress2%
Apr 2026Mar 2031

First Submitted

Initial submission to the registry

January 13, 2023

Completed
5 months until next milestone

First Posted

Study publicly available on registry

June 18, 2023

Completed
2.8 years until next milestone

Study Start

First participant enrolled

April 1, 2026

Completed
4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2030

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2031

Last Updated

June 4, 2025

Status Verified

May 1, 2025

Enrollment Period

4 years

First QC Date

January 13, 2023

Last Update Submit

May 29, 2025

Conditions

Keywords

Cardiopulmonary Resuscitationcardiopulmonary resuscitation trainingLay Rescuer cardiopulmonary resuscitationlay rescuer cardiopulmonary resuscitation training

Outcome Measures

Primary Outcomes (1)

  • CPR Skill Retention

    High-quality CPR as measured by compression rate (per minute), depth (inches), and correct hand placement. High-quality CPR is defined as correct rate (100-120/min) AND \>70% of compressions at appropriate depth (2-2.4inches) with appropriate hand placement.

    1-4 years

Secondary Outcomes (4)

  • CPR Attitudes

    1-4 years

  • CPR Knowledge Retention

    1-4 years

  • Emotional Profile

    1-4 years

  • Learner Engagement

    1-4 years

Other Outcomes (1)

  • Training Feature Effects (Contextualization, Gamification, Emotional Impact)

    1-4 years

Study Arms (9)

Every 2 year standard CPR training

ACTIVE COMPARATOR

Receives two 60-minute instructor-led CPR trainings: once in 9th grade and again in 11th grade

Behavioral: CPR Training

Annual Standard CPR training

ACTIVE COMPARATOR

Receives a 60-minute instructor-led CPR training each year for three years.

Behavioral: CPR Training

High-Frequency, Blended Training

ACTIVE COMPARATOR

Starts with a 30-minute serious game-based session, followed by 10-minute refreshers every semester for four years (8 total sessions).

Behavioral: CPR Training

Annual Serious Game Training

ACTIVE COMPARATOR

Receives a 30-minute serious game-based training session once per year for three years.

Behavioral: CPR Training

Control

NO INTERVENTION

No CPR training

Standard High-fidelity Manikin

ACTIVE COMPARATOR

Uses a commercially available torso manikin with realistic chest mechanics and feedback. Serves as the gold standard comparator for CPR training.

Device: CPR Manikin Type

Low-Fidelity Manikin

ACTIVE COMPARATOR

Uses a basic inflatable torso manikin with minimal feedback or resistance. Represents a low-cost, commonly used alternative in schools and communities.

Device: CPR Manikin Type

No-Head Manikin (Prototype)

ACTIVE COMPARATOR

Uses a custom-built spring-based device with a silicone topper and realistic force-displacement properties that closely mimic the human chest. Tests whether an affordable, biomechanically accurate prototype can improve compression quality.

Device: CPR Manikin Type

Non-Traditional Object

ACTIVE COMPARATOR

Uses improvised materials (e.g., toilet paper rolls) to simulate chest compressions. Evaluates the feasibility and effectiveness of ultra-low-cost CPR practice tools

Device: CPR Manikin Type

Interventions

CPR TrainingBEHAVIORAL

Various durations and frequencies of CPR training

Annual Serious Game TrainingAnnual Standard CPR trainingEvery 2 year standard CPR trainingHigh-Frequency, Blended Training

Various types of CPR manikins are compared

Low-Fidelity ManikinNo-Head Manikin (Prototype)Non-Traditional ObjectStandard High-fidelity Manikin

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • All students at participating schools

You may not qualify if:

  • Previous CPR training (will be included in the CPR training but excluded from analysis)
  • Physical injury which prevents performing CPR
  • Student or parent opt-out

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Nevada Reno

Reno, Nevada, 89557, United States

Location

MeSH Terms

Conditions

Out-of-Hospital Cardiac Arrest

Condition Hierarchy (Ancestors)

Heart ArrestHeart DiseasesCardiovascular Diseases

Study Officials

  • Lorrel Toft

    University of Nevada, Reno

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Lorrel Toft, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
The statistical analysis will be masked as to which intervention subjects received, with simple "A," "B," etc. designation.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Aim 1: A 4-year, cluster-randomized trial at a rural high school evaluates the impact of CPR training frequency and duration on skill retention, confidence, and emotional readiness. Students (N\~1,200) are assigned by class year to different training schedules using standard, gamified, or brief refresher formats. CPR skills, knowledge, and psychosocial outcomes are assessed annually. Aim 2: A 2-year, individually randomized trial at a suburban high school compares four chest compression practice tools: high-fidelity manikin, low-fidelity manikin, a novel "no-head" manikin, and improvised objects. Ninth-grade students (N\~432) are assessed post-training and at 1 year for CPR skill quality (rate, depth, recoil, hand placement) using objective measurement tools.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor of Medicine

Study Record Dates

First Submitted

January 13, 2023

First Posted

June 18, 2023

Study Start

April 1, 2026

Primary Completion (Estimated)

March 31, 2030

Study Completion (Estimated)

March 31, 2031

Last Updated

June 4, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

All data is gathered and reported in de-identified, aggregate form, per IRB and school official direction.

Locations