Evaluation of Efficacy of Online Real-time Home CPR Training Program

Summary

The purpose of this study is to evaluate the effectiveness of a real-time home CPR(cardiopulmonary resuscitation) training program. The study participants will be allocated to two different CPR training programs. The intervention group will participate in the real-time home CPR training program while the control group will participate in the conventional CPR training program. The investigators will compare the quality of chest compression between the two study groups. The investigators hypothesize that the new real-time home CPR training program is non-inferior to the preexisting conventional CPR training program.

Conditions

• Cardiopulmonary Resuscitation
• Cardiopulmonary Arrest
• Education

Interventions

OTHER

Real-time home CPR training

The participants in the intervention group will have Little Anne QCPR mannequins (Laerdal, Stavanger, Norway) delivered to their homes. The participants will use an online platform specifically developed for CPR training (HEROS Remote app). The training program will provide video-based self-instruction training followed by hands-on chest compression training with the instructor. The hands-on chest compression training session provides real-time chest compression quality measurement followed by real-time feedback from the instructor. Chest compression quality will be measured by Little Anne QCPR mannequins.

OTHER

Conventional CPR training

Participants in the conventional CPR training program group will be provided CPR education with the "Home Education and Resuscitation Outcome Study (HEROS)" program that is currently provided in Seoul, Korea. The HEROS program is a 1-hour training course, consisting of a 30-minute video-based self-instruction training with a mannequin. The program also includes a bystander CPR simulation with a simulated dispatcher using the participants own cell phone. Little Anne QCPR mannequins will be provided to measure and give feedback on the participants chest compression performance.

Sponsors & Collaborators

• Seoul National University Hospital

  lead OTHER

Principal Investigators

• Ki Jeong Hong, MD · Department of Emergency Medicine, Seoul National University Hospital

• STEPHEN GW LEE, MD · Department of Emergency Medicine, SMG-SNU Boramae Medical Center

• Seulki Choi, MD · Department of Emergency Medicine, Seoul National University Hospital

Study Design

Allocation

NON_RANDOMIZED

Purpose

OTHER

Masking

NONE

Model

PARALLEL

Eligibility

Min Age

18 Years

Max Age

65 Years

Sex

ALL

Healthy Volunteers

Yes

Timeline & Regulatory

Start

2021-08-26

Primary Completion

2021-12-31

Completion

2022-08-31

Countries

• South Korea

Study Locations