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NCT Number: NCT07666867

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

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.

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • 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)

Treatment and study plan

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.

Other names: Virtual Reality, CF-CBT

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

Other names: Control

Primary outcomes

  1. Self-compassion

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

    Self-compassion will be assessed using the Self-Compassion Scale (SCS), as it reflects a core therapeutic target of the CF-CBT-based techniques

Secondary outcomes

  1. Burnout

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

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

  2. Secondary Traumatic Stress (STS)

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

    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

Study contacts

Contact information is provided by the study sponsor or research team.

Rawan Iriqat

CONTACT

[email protected]

(858) 534-2230

Sponsors and collaborators

Lead sponsor

University of California, San Diego

Other

Registry information

Acronym: VR-CF-CBT

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Jun 24, 2026
Registry last updated
Jun 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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