Assessing the Impact of VR-Based Observational Mindfulness Meditation on Stress Reduction in Adults
Part of paid clinical trials in Erie, Pennsylvania.
- Sponsor
- Penn State University
- Study ID
- NCT06704282
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Anxiety
- Depression
- Stress
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- VR Mindfulness Meditation Program — BEHAVIORALA 15-minute guided mindfulness meditation session conducted in a virtual reality environment to enhance stress reduction and mindfulness.
Study Details
This study investigates the impact of a mindfulness-based intervention using virtual reality (VR) and artificial intelligence (AI) coaching on stress reduction. Participants will engage in VR-based observation mindfulness activities guided by an AI coach. The study aims to evaluate the effectiveness of this intervention compared to a standard relaxation process by measuring self-reported stress levels, physiological biomarkers (e.g., heart rate), and participant satisfaction. The research could inform the development of future digital mental health interventions.
Key Dates
- Start date
- Nov 25, 2024
- Status verified
- Nov 2024
- Primary completion
- Jan 31, 2025
- Completion
- Feb 23, 2025
Study Design
- Enrollment
- 34 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Mindfulness Meditation GroupParticipants in this arm will undergo a 15-minute VR-based mindfulness observational meditation session guided by a virtual coach. The intervention focuses on promoting mindfulness and reducing stress through structured guidance in a controlled virtual environment.
Primary Outcome Measure
Reduction in Perceived Stress Levels [ Time Frame: Immediately post-intervention (Day 1, 15 minutes after the session ends). ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Penn State Univercity | Erie | Pennsylvania | 16563 |
Find similar trials in Erie, PA
Related Studies
- Evaluation of the PACE/PACENET BHL Clinical ProgramRecruiting · University of Pennsylvania · Philadelphia, Pennsylvania
- Decoding and Modulating Affective Brain StatesRecruiting · University of Pennsylvania · Philadelphia, Pennsylvania
- Collaborative Care Intervention for Cancer Patients and Their Family Caregivers -LITENot Yet Recruiting · University of Pittsburgh · Pittsburgh, Pennsylvania
- RXWell to Decrease Post-Operative Opioid Use in Total Knee or Hip ArthroplastyRecruiting · University of Pittsburgh · Monroeville, Pennsylvania