Virtual Reality for Enhancing Self Compassion and Reducing Burnout Among Healthcare Providers
VR-CF-CBT
1 other identifier
interventional
52
0 countries
N/A
Brief Summary
Healthcare providers in high-demand clinical settings are at high risk for burnout and secondary traumatic stress due to repeated exposure to patient trauma, which can compromise well-being and quality of care. Compassion-focused cognitive behavioral therapy (CF-CBT) can reduce stress and enhance self-compassion, but traditional delivery is time- and resource-intensive. This project evaluates the feasibility, acceptability, and potential effectiveness of virtual reality (VR)-enhanced CF-CBT specifically adapted for healthcare providers experiencing vicarious trauma. Grounded in Neff's self-compassion framework (emphasizing self-kindness, common humanity, and mindfulness) the VR intervention provides 8 immersive environments where participants can practice compassion-focused skills, engage in procedural learning, and regulate emotional responses in real time. The study will be conducted at UC San Diego Health using a two-arm randomized design comparing VR-enhanced CF-CBT with self-guided compassion-focused CBT/mindfulness exercises delivered without VR. Participants will complete 8 brief VR interventional sessions (approximately 6-10 minutes each) over 4-6 weeks. Outcomes include self-compassion, burnout, and secondary traumatic stress, measured using validated instruments. Feasibility and acceptability will be evaluated through recruitment, retention, session completion, engagement, and participant feedback. Findings will provide preliminary evidence for VR-enhanced compassion-focused interventions as a scalable and accessible approach to supporting healthcare providers' emotional well-being in demanding clinical environments, and will inform future cultural adaptation and implementation in low-resource and conflict-affected healthcare settings such as those in post-war zones.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 18, 2026
CompletedFirst Posted
Study publicly available on registry
June 24, 2026
CompletedStudy Start
First participant enrolled
July 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 1, 2027
June 24, 2026
June 1, 2026
3 months
June 18, 2026
June 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Self-compassion
Self-compassion will be assessed using the Self-Compassion Scale (SCS), as it reflects a core therapeutic target of the CF-CBT-based techniques
Baseline assessment (T0), Post-Intervention assessment (T1), and 6 weeks post-intervention assessment (T2)
Secondary Outcomes (2)
Burnout
Baseline assessment (T0), Post-intervention assessment (T1), 6 weeks post-intervention (T2)
Secondary Traumatic Stress (STS)
Baseline assessment (T0), Post-intervention assessment (T1), 6 weeks post-intervention (T2)
Study Arms (2)
Virtual Reality enhanced Compassion Focused Cognitive Behavioral Therapy
ACTIVE COMPARATORThis arm will receive a fixed number of immersive compassion focused cognitive behavioral therapy sessions delivered via virtual reality headsets.
Control Group
PLACEBO COMPARATORThis arm will receive compassion focused cognitive behavioral therapy delivered via psychoeducational booklets.
Interventions
The intervention group will undergo a fixed number of immersive compassion focused cognitive behavioral therapy sessions delivered via virtual reality headsets.
This arm will receive the same order and frequency of compassion focused cognitive behavioral therapy sessions delivered via digital booklets
Eligibility Criteria
You may qualify if:
- have at least one year of experience working in a healthcare setting
You may not qualify if:
- participating in other behavioral interventions that could confound study results
- auditory or visual impairments that would interfere with VR usage
- Participants who experience clinically significant VR-related discomfort/motion sickness as assessed by the Simulator Sickness Questionnaire (SSQ)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Wael Al-Delaimy, PhD, MD
University of California, San Diego
- STUDY CHAIR
Andre Faro, PhD
Universidade Federal de Sergipe
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
June 18, 2026
First Posted
June 24, 2026
Study Start
July 1, 2026
Primary Completion (Estimated)
October 1, 2026
Study Completion (Estimated)
February 1, 2027
Last Updated
June 24, 2026
Record last verified: 2026-06