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

Not Applicable

Completed

• Conditions: Cardiopulmonary Resuscitation; Education; Cardiopulmonary Arrest
• Interventions: Other: Conventional CPR training; Other: Real-time home CPR training

• Registration Number: NCT05023616
• Lead Sponsor: Seoul National University Hospital

Brief 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.

Detailed Description

Bystander CPR(cardiopulmonary resuscitation) is important for the survival of out-of-hospital cardiac arrest patients. CPR training for the general public is important to improve the rate and quality of bystander CPR. Conventional CPR education was conducted under face-to-face contact with instructors and multiple trainees gathered at a training center, but after the coronavirus disease 2019 pandemic, face-to-face training became difficult. To overcome this limitation the investigators have developed a new real-time home CPR training program. The training program delivers Little Anne QCPR mannequins (Laerdal, Stavanger, Norway) to each participants homes and the participants use an application specifically developed for CPR training that automatically connects wirelessly to the Little Anne QCPR mannequin through Bluetooth so that the instructor can give real-time feedback on chest compression quality to participants.

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. Chest compression quality at the start of both training programs and after completion of the programs will be measured by Little Anne QCPR mannequins used in the training programs. The investigators hypothesize that the new real-time home CPR training program is non-inferior to the preexisting conventional CPR training program.

Study Timeline

• Study First Submitted: 2021-08-06
• Study First Submitted QC: 2021-08-20
• Study Start: 2021-08-26
• Study First Posted: 2021-08-26
• Primary Completion: 2021-12-31
• Study Completion: 2022-08-31
• Status Verified: 2022-10
• Last Update Submitted: 2022-10-24
• Last Update Posted: 2022-10-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 180

Inclusion Criteria

• Adults without prior CPR training within 6 months

Exclusion Criteria

• Healthcare providers

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Conventional CPR training	Conventional CPR training	Conventional CPR training will be provided to participants
Real-time home CPR training	Real-time home CPR training	Online real-time home CPR(cardiopulmonary resuscitation) training will be provided to participants

Primary Outcome Measures

Name	Time	Method
Average compression depth	Immediately after the training program has been completed, participants will be asked to perform chest compression for 2 minutes. The outcome measure will be collected from the 2 minutes of chest compression at this point.	Average compression depth of chest compression performed for 2 minutes

Secondary Outcome Measures

Name	Time	Method
Proportion of adequate compression depth	Immediately after the training program has been completed, participants will be asked to perform chest compression for 2 minutes. The outcome measure will be collected from the 2 minutes of chest compression at this point.	Proportion of adequate compression depth performed for 2 minutes
Average compression rate	Immediately after the training program has been completed, participants will be asked to perform chest compression for 2 minutes. The outcome measure will be collected from the 2 minutes of chest compression at this point.	Average compression rate of chest compression performed for 2 minutes
Proportion of adequate compression rate	Immediately after the training program has been completed, participants will be asked to perform chest compression for 2 minutes. The outcome measure will be collected from the 2 minutes of chest compression at this point.	Proportion of adequate compression rate performed for 2 minutes
No-flow fraction	Immediately after the training program has been completed, participants will be asked to perform chest compression for 2 minutes. The outcome measure will be collected from the 2 minutes of chest compression at this point.	Proportion of no-flow time during 2 minutes of chest compression

Trial Locations

Locations (1)

Seoul National University Hospital; 🇰🇷 Seoul, Korea, Republic of