Virtual Reality Mindfulness for Burnout
Trial Summary
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications.
What data supports the effectiveness of the treatment Virtual Reality Mindfulness intervention for burnout?
Research suggests that Virtual Reality (VR) can make mindfulness exercises more engaging and effective by creating an immersive experience, which may help reduce burnout symptoms. Additionally, VR-based mindfulness has shown promise in reducing negative emotions like sadness, anger, and anxiety, which are often associated with burnout.12345
Is Virtual Reality Mindfulness safe for humans?
Research suggests that Virtual Reality Mindfulness is generally safe for humans, with participants reporting improvements in mood and reductions in negative emotions like sadness, anger, and anxiety. However, one study noted the potential for simulator sickness, which could affect user engagement.12456
How does the Virtual Reality Mindfulness treatment differ from other treatments for burnout?
Virtual Reality Mindfulness is unique because it uses immersive technology to enhance mindfulness practice, making it easier for participants to engage and stay focused. This approach can increase the sense of presence and reduce distractions, which may be particularly beneficial for individuals experiencing burnout who struggle with traditional mindfulness exercises.12478
What is the purpose of this trial?
A pilot intervention wait-list control study evaluating the effectiveness of a worksite, on-demand virtual reality mindfulness intervention. Outcomes of interest include perceived stress, burnout, work engagement, resilience and respiratory rates. System usability of the VR mindfulness program and integration into the clinical workday will also be assessed for both groups.
Eligibility Criteria
This trial is for nurse managers experiencing work-related stress and burnout. Participants should be interested in trying a virtual reality mindfulness program during their workday to improve stress levels, engagement, resilience, and breathing patterns.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Intervention
Participants in the intervention group receive an 8-week on-demand virtual reality mindfulness-based intervention
Wait-list Control
Participants in the wait-list control group receive the virtual reality mindfulness intervention during the second 8 weeks
Follow-up
Participants are monitored for outcomes such as perceived stress, burnout, and work engagement after the intervention
Treatment Details
Interventions
- Virtual Reality Mindfulness intervention
Find a Clinic Near You
Who Is Running the Clinical Trial?
Ohio State University
Lead Sponsor