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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05908500
Other study ID # CPRTrainer2023
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2024
Est. completion date January 2, 2028

Study information

Verified date June 2023
Source University of Nevada, Reno
Contact Lorrel Toft, MD
Phone 4103028456
Email ltoft@unr.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this prospective trial is to compare CPR skill and attitudes in adolescent students. The main question[s] it aims to answer are: - Does a gamified CPR experience improve CPR skill retention compared to standard classroom CPR training? - Does a gamified CPR experience improve attitudes/knowledge relating to barriers for women and minorities receiving CPR? Participants will - Answer pre-training questionnaires - Participate in CPR training - Participate in CPR skills testing on the day of training, and at 4-6 months - Answer post-training questionnaires Researchers will compare standard CPR classroom training to the novel gamified CPR training experience, which includes an interactive film, a CPR Trainer spring, and a mobile device app.


Description:

We will investigate the effectiveness of the gamified CPR experience (Trainer + app + film + software). The study will be a prospective, cluster-randomized controlled trial with 2 arms: control (standard instructor-led CPR training), and gamified experience. The intervention and cluster randomization will occur at the classroom level and outcomes reported at the individual level. We assume negligible intra-class correlation because classes will be randomized in an alternating fashion to eliminate time-of-day differences. For example, 1st period is randomized to control, 2nd period to game. CPR training (control or game method) will occur at the beginning of each semester in 8th or 9th grade Health class. Immediately after training, students will perform 2-min of CC, while the app silently measures CC rate and depth. Pre- and post-training questionnaires assessing knowledge and response to female-specific and ethnic CPR barriers will be administered via paper-pencil. At the end of the semester (4 months), students will again perform 2-min of CC and answer questionnaires. All data will be collected on-site in paper-pencil format, and entered into Excel by research coordinator off-site. All data will be de-identified and reported in aggregate form


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date January 2, 2028
Est. primary completion date January 1, 2027
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - All 8th and 9th grade students at participating schools enrolled in Health Class. Exclusion Criteria: - 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

Study Design


Intervention

Other:
CPR Training
Various methods of CPR training are implemented and compared

Locations

Country Name City State
United States University of Nevada Reno Reno Nevada

Sponsors (1)

Lead Sponsor Collaborator
University of Nevada, Reno

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary CPR Skill Retention High-quality CPR as measured by compression rate (per minute) and depth (inches). High-quality CPR is defined as correct rate (100-120/min) AND >70% of compressions at appropriate depth (2-2.4inches). 4-6 months
Secondary CPR Attitudes A novel questionnaire developed for the study asks Likert-scale questions (scale of 1 to 5, with 5 being VERY LIKELY and 1 being VERY UNLIKELY) regarding attitudes towards performing CPR and overcoming barriers to performing CPR. 4-6 months
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