Official Title
Development of Virtual Reality Treatment Technology to Treat Trauma Related to COVID-19 Infection
Brief Summary

This clinical trial aims to develop and evaluate the effectiveness of virtual reality(VR)-based exposure therapy for trauma symptoms related to COVID-19 infection. Theintervention targets healthcare workers and individuals from the general population whoexperienced pandemic-related psychological distress. The study assesses psychological andphysiological outcomes, including PTSD, anxiety, depression, HRV, and EEG biomarkers.

Detailed Description

The project involves a two-phase clinical study. In Phase 1, VR exposure therapy content
is developed based on trauma management theory and tailored to specific participant
groups (e.g., COVID-19 survivors, healthcare workers). In Phase 2, randomized controlled
trials will compare VR treatment with standard therapy approaches (CBT, supportive
therapy) across two populations:

Healthcare workers involved in the care of COVID-19 patients Members of the general
public affected by social disaster-related psychological distress

Participants will undergo 5 weekly sessions of VR exposure therapy. Pre- and
post-intervention assessments will include standardized psychiatric scales (e.g., PHQ-9,
PCL-5), HRV, and EEG measurements. The trial aims to validate the efficacy and safety of
customized VR therapy protocols and identify relevant biomarkers for treatment
prediction.

Not yet recruiting
PTSD
PTSD Symptoms

Behavioral: VR Exposure Therapy

Virtual Reality Exposure Therapy (VRET) is a form of psychotherapy that uses immersive
virtual environments to simulate trauma-related stimuli in a controlled and safe setting,
allowing individuals to gradually confront and process distressing memories or triggers.

VRET is grounded in prolonged exposure (PE) therapy, a well-established treatment for
PTSD and anxiety disorders.

In this study, VRET is delivered in 5 weekly sessions, each lasting approximately 50
minutes, using a customized VR system.

Sessions are tailored based on participant group (e.g., COVID-19 survivor vs. healthcare
worker).

Each session includes psychoeducation, exposure to individualized trauma-related virtual
scenes, and guided emotional processing.

The system incorporates eye-tracking, breathing exercises, and real-time subjective
distress scaling (SUDs) to monitor engagement and safety.

Behavioral: Cognitive Behavioral Therapy (CBT)

Face-to-face CBT with exposure elements, targeting trauma-related symptoms. Administered
in 5 weekly sessions.

Behavioral: Supportive Psychotherapy

Therapist-led supportive therapy (TAU), focusing on empathy, validation, and emotional
support without structured exposure.

Eligibility Criteria

Inclusion Criteria:

- Age 18-64, healthy population who survived from COVID-19 (COVID survivors) or
Healthcare Workers with PCL-5 ≥10, GAD-7/PHQ-9 ≥10

Exclusion Criteria:

- Pregnancy, neurological disorders, severe medical conditions

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 64 Years
Locations

Not Provided

Contacts

Ji Sun Kim, MD, PhD
82-10-9933-1286
ideal91@hanmail.net

Min Jung Park, RN
+82-10-4115-2642
0705pmj@naver.com

Ji Sun Kim, MD, PhD, Principal Investigator
Soonchunhyang University Hospital

Soonchunhyang University Hospital
NCT Number
Keywords
VR exposure
PTSD symptoms
COVID 19
MeSH Terms
Stress Disorders, Post-Traumatic
COVID-19
Cognitive Behavioral Therapy