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

Sponsor
Seoul National University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05023616
Collaborator
(none)
180
1
2
12
15

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Real-time home CPR training
  • Other: Conventional CPR training
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
180 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Evaluation of Efficacy of Online Real-time Home CPR Training Program : a Randomized Open-label Clinical Trial
Actual Study Start Date :
Aug 26, 2021
Anticipated Primary Completion Date :
Aug 25, 2022
Anticipated Study Completion Date :
Aug 26, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Real-time home CPR training

Online real-time home CPR(cardiopulmonary resuscitation) training will be provided to participants

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.

Active Comparator: Conventional CPR training

Conventional CPR training will be provided to participants

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.

Outcome Measures

Primary Outcome Measures

  1. 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

  1. 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

  2. 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

  3. 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

  4. 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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Adults without prior CPR training within 6 months
Exclusion Criteria:
  • Healthcare providers

Contacts and Locations

Locations

Site City State Country Postal Code
1 Seoul National University Hospital Seoul Korea, Republic of 03080

Sponsors and Collaborators

  • Seoul National University Hospital

Investigators

  • Study Chair: Ki Jeong Hong, MD, Department of Emergency Medicine, Seoul National University Hospital
  • Principal Investigator: STEPHEN GW LEE, MD, Department of Emergency Medicine, SMG-SNU Boramae Medical Center
  • Principal Investigator: Seulki Choi, MD, Department of Emergency Medicine, Seoul National University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ki Jeong Hong, Clinical associate professor, Seoul National University Hospital
ClinicalTrials.gov Identifier:
NCT05023616
Other Study ID Numbers:
  • H-2107-205-1239
First Posted:
Aug 26, 2021
Last Update Posted:
Sep 1, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ki Jeong Hong, Clinical associate professor, Seoul National University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 1, 2021