About this trial
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. The intervention targets healthcare workers and individuals from the general population who experienced pandemic-related psychological distress. The study assesses psychological and physiological outcomes, including PTSD, anxiety, depression, HRV, and EEG biomarkers.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age 18-64, healthy population who survived from COVID-19 (COVID survivors) or Healthcare Workers with PCL-5 ≥10, GAD-7/PHQ-9 ≥10
Disqualifiers
Pregnancy, neurological disorders, severe medical conditions
Trial design
Parallel
Treatments tested in this trial
VR Exposure Therapy
BehavioralVirtual 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.
Cognitive Behavioral Therapy (CBT)
BehavioralFace-to-face CBT with exposure elements, targeting trauma-related symptoms. Administered in 5 weekly sessions.
Supportive Psychotherapy
BehavioralTherapist-led supportive therapy (TAU), focusing on empathy, validation, and emotional support without structured exposure.
Treatment groups
Trial outcomes
Primary outcomes
Change in PTSD symptoms
Change in PTSD symptoms (PCL-5/CAPS-5) at baseline, week 5, 3-mo follow-up
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: