AzTrials
AzTrials

Burnout, Healthcare WorkersVR-CF-CBTNCT07666867

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

A study testing Compassion focused cognitive behavioral therapy sessions delivered via virtual reality headsets and Compassion focused cognitive behavioral therapy app based booklet in people with Burnout, Healthcare Workers and Burnout, run by University of California, San Diego.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
Search all trials

Trial 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. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
What is being tested?
Compassion focused cognitive behavioral therapy sessions delivered via virtual reality headsets and Compassion focused cognitive behavioral therapy app based booklet
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
52 participants
Where
No sites listed yet
Study dates
1 Jul 2026to 1 Feb 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

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

Who cannot join

  • 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 locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

About this study

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.

Being tested
Compassion focused cognitive behavioral therapy sessions delivered via virtual reality headsets, Compassion focused cognitive behavioral therapy app based booklet
Keywords
Self-Compassion, Empathy, CBT, Virtual Reality, Healthcare Provider Burnout
Medical subject headings
Burnout, Psychological

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

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

    Also called Virtual Reality, CF-CBT

    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 bookletBehavioural

    Also called Control

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

Study groups in NCT07666867
Study groupRoleWhat they receive
Virtual Reality enhanced Compassion Focused Cognitive Behavioral TherapyActive comparatorThis arm will receive a fixed number of immersive compassion focused cognitive behavioral therapy sessions delivered via virtual reality headsets.
Receives: Behavioral: Compassion focused cognitive behavioral therapy sessions delivered via virtual reality headsets
Control GroupPlacebo comparatorThis arm will receive compassion focused cognitive behavioral therapy delivered via psychoeducational booklets.
Receives: Behavioral: Compassion focused cognitive behavioral therapy app based booklet

What is being measured

The primary outcome is the main question the study is designed to answer.

  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

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

Secondary outcomes (2)
  1. Burnout

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

    Measured: 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

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jun 2026
  2. Study start1 Jul 2026 (estimated)
  3. Primary completion1 Oct 2026 (estimated)
  4. Study completion1 Feb 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
52 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07666867
Sponsor's protocol ID
814637
Acronym
VR-CF-CBT
Status last verified
Jun 2026
First submitted
18 Jun 2026
Last updated
24 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Iriqat R, Faro A, Tarle S, Moore S, Al-Delaimy W. Virtual Reality for Enhancing Self-Compassion and Reducing Burnout Among Mental Health Care Professionals: Protocol for a Pilot Feasibility Randomized Controlled Trial. JMIR Res Protoc. 2026 Oct 19;15:e105754. doi: 10.2196/105754.

    PubMed 42896176

Questions about this trial

What is this clinical trial studying?

A study testing Compassion focused cognitive behavioral therapy sessions delivered via virtual reality headsets and Compassion focused cognitive behavioral therapy app based booklet in people with Burnout, Healthcare Workers and Burnout, run by University of California, San Diego.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 24 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Rawan Iriqat ((858) 534-2230, ririqat@health.ucsd.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Self-compassion (time frame: Baseline assessment (T0), Post-Intervention assessment (T1), and 6 weeks post-intervention assessment (T2)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07666867, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2026.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in