Efficacy of Online Real-time CPR Training

Sponsor
Seoul National University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04656405
Collaborator
(none)
180
1
3
15.6
11.5

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the effectiveness of a new online real-time quality measurement and feedback video-based CPR training program. The study participants will be allocated to three different CPR training programs: online real-time quality measurement and feedback video-based CPR training program, online real-time feedback video-based CPR training without quality measurement program, and conventional CPR training program. After CPR training, each participant will perform a 6 minute CPR simulation test. The investigators will compare the quality of chest compression between the three study groups. The investigators hypothesize that the new online real-time quality measurement and feedback video-based CPR training program is non-inferior to the preexisting conventional CPR training program and is superior to online real-time feedback video-based CPR training without quality measurement.

Condition or Disease Intervention/Treatment Phase
  • Other: Online real-time quality measurement and feedback video-based CPR training
  • Other: Online real-time feedback video-based CPR training without quality measurement
  • Other: Conventional CPR training
N/A

Detailed Description

Bystander CPR 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. Preexisting CPR education was conducted under face-to-face contact with instructors and multiple trainees gathering 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 online real-time quality measurement and feedback video-based CPR training program that uses online video conferencing, Little Anne QCPR mannequin (Laerdal, Stavanger, Norway) and SkillGuide (Laerdal, Stavanger, Norway) device.

The purpose of this study is to evaluate the effectiveness of a new online real-time quality measurement and feedback video-based CPR training program. To evaluate the effectiveness of the new CPR training program the investigators propose to conduct a randomized clinical trial with three arms: online real-time quality measurement and feedback video-based CPR training program, online real-time feedback video-based CPR training without quality measurement program, and conventional CPR training program. 60 non healthcare provider, healthy adult volunteers will be randomized to each study arm. After CPR training, each participant will perform a 6 minute CPR simulation test. The investigators will measure the depth and rate of chest compression, hand positioning during chest compression, no-flow time and start to chest compression time.

The primary outcome of the study is mean chest compression depth. Chest compression rate, hand position, total no flow time, and time to chest compression will also be measured. The investigators hypothesize that the new online real-time quality measurement and feedback video-based CPR training program is non-inferior to the preexisting conventional CPR training program and is superior to online real-time feedback video-based CPR training without quality measurement.

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 Quality Measurement and Feedback Video-based CPR Training Program
Actual Study Start Date :
Dec 11, 2020
Anticipated Primary Completion Date :
Dec 30, 2021
Anticipated Study Completion Date :
Mar 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Online real-time CPR training program

Online real-time quality measurement and feedback video-based CPR training will be provided to participants

Other: Online real-time quality measurement and feedback video-based CPR training
Participants in the online real-time quality measurement and feedback video-based CPR training program group will access an online training center with laptop computers provided by the researcher. All education and communication is conducted online. The study instructors shows the study participants an edited version of the CPR training video used in the conventional CPR training program. A Little Anne QCPR mannequin (Laerdal, Stavanger, Norway) and SkillGuide (Laerdal, Stavanger, Norway) are provided so that the participants can use while watching the video and during the following hands-on practice session. After watching the video, hands-on practice will be conducted by the instructor on-line. The instructor will watch each individual participants CPR performance via video conferencing and collect real-time performance data using the QCPR mannequin device. Using this information, the instructor will provide real-time online feedback to participants.

Active Comparator: Online real-time CPR training without quality measurement program

Online real-time feedback video-based CPR training without quality measurement will be provided to participants

Other: Online real-time feedback video-based CPR training without quality measurement
Participants in the online real-time feedback video-based CPR training without quality measurement program group will access an online training center with laptop computers provided by the researcher. All education and communication is conducted online. When study participants access the online training center, study instructors shows the study participants an edited version of the CPR training video used in the conventional CPR training program. A Little Anne QCPR mannequin (Laerdal, Stavanger, Norway) is provided so that the participants can use while watching the video and during the following hands-on practice session. After watching the video, hands-on practice will be conducted by the instructor on-line. The instructor will watch each individual participants CPR performance via video conferencing. The instructor will provide real-time online feedback to participants.

Placebo Comparator: Conventional CPR training program

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 mannequin (Laerdal, Stavanger, Norway) and SkillGuide (Laerdal, Stavanger, Norway) device are provided to measure and give feedback on the participants CPR performance.

Outcome Measures

Primary Outcome Measures

  1. Chest compression depth [Assessed during 6 minute CPR simulation test]

    Depth of chest compressions measured in millimeters

Secondary Outcome Measures

  1. Chest compression rate [Assessed during 6 minute CPR simulation test]

    Rate of chest compression per minute

  2. Hand position [Assessed during 6 minute CPR simulation test]

    Correct hand position measured by QCPR mannequin

  3. No flow time [Assessed during 6 minute CPR simulation test]

    Time with no chest compression after start of chest compression

  4. Time to chest compression [Assessed during 6 minute CPR simulation test]

    Time from start of simulation to start of chest compression

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Volunteers aged 18 years or older
Exclusion Criteria:
  • Healthcare providers

  • Participants with chronic lung diseases

  • Participants with cardiovascular diseases

  • Participants with visual disabilities

  • Participants with hearing disabilities

  • Participants with musculoskeletal disabilities

Contacts and Locations

Locations

Site City State Country Postal Code
1 Seoul Metropolitan Government-Seoul National University Borame Medical Center Seoul Korea, Republic of 07061

Sponsors and Collaborators

  • Seoul National University Hospital

Investigators

  • Study Chair: TAE HAN KIM, MD, SMG-SNU Boramae Medical Center
  • Principal Investigator: STEPHEN GW LEE, MD, Seoul National University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Tae Han Kim, Clinical Assistant Professor, Seoul National University Hospital
ClinicalTrials.gov Identifier:
NCT04656405
Other Study ID Numbers:
  • 30-2020-232
First Posted:
Dec 7, 2020
Last Update Posted:
May 18, 2021
Last Verified:
May 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 Tae Han Kim, Clinical Assistant Professor, Seoul National University Hospital

Study Results

No Results Posted as of May 18, 2021