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Evaluation of Effectiveness of Virtual Reality-based Dispatcher Assisted Cardiopulmonary Resuscitation Training

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Seoul National University

Status

Completed

Conditions

Cardiac Arrest

Treatments

Behavioral: HEROS VR CPR training program
Behavioral: Conventional HEROS CPR training program

Study type

Interventional

Funder types

Other

Identifiers

NCT06226246
0420232290

Details and patient eligibility

About

This study aims to compare the effect of conventional cardiopulmonary resuscitation (CPR) training and CPR training with added virtual reality (VR) on trainee self-efficacy.

Full description

This study aims to compare the conventional cardiopulmonary resuscitation (CPR) training program (HEROS CPR training program) with the HEROS VR (virtual reality) CPR training program to which the newly developed VR curriculum was added. The experimental group is the HEROS VR training group, and CPR training is conducted for approximately 60 minutes for 6 to 8 trainees per training. At the start and the end of the training, students are taught about cardiac arrest, recognition of emergency situations, and reporting to 119 by watching VR, and in the middle part, they practice chest compressions by watching conventional HEROS video. The control group is the existing HEROS training group. To control variables, the number of trainees per training was limited to 6 to 8, and the existing video-based CPR training was implemented. The investigators will conduct a Modified Basic Resuscitation Skills Self-Efficacy scale survey before and after training to compare the difference in the improvement of trainees' self-efficacy evaluation of CPR after CPR training in the HEROS VR curriculum and the existing HEROS curriculum.

Enrollment

75 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Non-medical personnel aged 18~65

Exclusion criteria

  • Who have received CPR training within the past 1 year.
  • For whom it is difficult to wear the VR equipment due to a history of side effects or problems such as head trauma.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

75 participants in 2 patient groups

HEROS VR
Experimental group
Description:
Trainee trained by HEROS VR CPR training program
Treatment:
Behavioral: HEROS VR CPR training program
Conventional HEROS
Active Comparator group
Description:
Trainee trained by conventional HEROS CPR training program
Treatment:
Behavioral: Conventional HEROS CPR training program

Trial contacts and locations

1

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Central trial contact

STEPHEN LEE, MD, MA

Data sourced from clinicaltrials.gov

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