Actively Recruiting

Age: 12Years - 25Years
All Genders
ID04493970

Assessment of Factors Impacting High School Students Mandatory Universal Student Instruction in Cardiopulmonary Resuscitation Appraised Learning- Is the Mandate Working? (The High School MUSICAL Study)

Led by Kansas City Heart Rhythm Research Foundation · Updated on 2024-10-26

5000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how mandatory cardiopulmonary resuscitation (CPR) education affects high school students. The study aims to provide valuable information to state health and education departments to improve CPR training programs and to explore partnerships that can enhance CPR education. It focuses on sudden cardiac arrest awareness and the ability of high school students to learn and retain CPR skills. Participants will complete a voluntary survey to evaluate how well high school students retain CPR knowledge and understand the training they received. The study observes factors that influence comprehension without administering any treatments or interventions. This observational approach helps identify national patterns in CPR education efforts among youth. During the study, students will be asked to complete surveys assessing their CPR knowledge and skill retention. Researchers will analyze these responses to measure the effectiveness of CPR training and identify elements that impact learning. The primary outcome is to assess retention and comprehension over seven months, with no additional treatments or procedures involved. Participation is expected to last according to the study timeline ending in October 2024.

CONDITIONS

Brief Title

HS Students Mandatory Universal Student Instruction in CPR Appraised Learning- Is the Mandate Working?

Who Can Participate

Age: 12Years - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • High school students completing voluntary survey
Not Eligible

You will not qualify if you...

  • Inability to give consent
  • Inability to complete survey

AI-Screening

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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 or remote) to complete eligibility assessment and consent

Diagnostic Evaluation

Duration - Up to 7 months

Participants complete a voluntary survey to assess retention, effectiveness, and factors impacting comprehension of CPR training.

1 or more survey completion sessions depending on study design

Trial Site Locations

Total: 1 location

1

Kansas City Heart Rhythm Institute

Overland Park, Kansas, United States, 66211

Actively Recruiting

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Research Team

D

Donita Atkins

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Importance and implementation of training in cardiopulmonary resuscitation and automated external defibrillation in schools: a science advisory from the American Heart Association.

Diana M Cave, Tom P Aufderheide, Jeff Beeson...

https://pubmed.ncbi.nlm.nih.gov/21220728

Cardiopulmonary resuscitation performed by bystanders does not increase adverse effects as assessed by chest radiography.

E Oschatz, P Wunderbaldinger, F Sterz...

https://pubmed.ncbi.nlm.nih.gov/11429353