Virtual Reality for Enhancing Self Compassion and Reducing Burnout Among Healthcare Providers

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorUniversity of California, San Diego

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

have at least one year of experience working in a healthcare setting

Disqualifiers

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)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Compassion focused cognitive behavioral therapy sessions delivered via virtual reality headsets

    Behavioral

    The intervention group will undergo a fixed number of immersive compassion focused cognitive behavioral therapy sessions delivered via virtual reality headsets.

  • Compassion focused cognitive behavioral therapy app based booklet

    Behavioral

    This arm will receive the same order and frequency of compassion focused cognitive behavioral therapy sessions delivered via digital booklets

Treatment groups

52 Participants
are divided into 2 treatment groups
Group A: Virtual Reality enhanced Compassion Focused Cognitive Behavioral TherapyActive comparator 1 intervention
Group B: Control GroupPlacebo comparator 1 intervention

Trial outcomes

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

Time frame
Baseline assessment (T0), Post-Intervention assessment (T1), and 6 weeks post-intervention assessment (T2)

Secondary outcomes

1

Burnout

Burnout will be assessed using the Maslach Burnout Inventory (MBI)

Time frame
Baseline assessment (T0), Post-intervention assessment (T1), 6 weeks post-intervention (T2)
2

Secondary Traumatic Stress (STS)

Vicarious (secondary) trauma will be assessed using Secondary Traumatic Stress Scale (STSS) with ProQOL-STS subscale, both of which are validated tools in healthcare settings, especially for providers exposed to chronic occupational stress and trauma

Time frame
Baseline assessment (T0), Post-intervention assessment (T1), 6 weeks post-intervention (T2)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: