Utilization of Virtual Reality Mindfulness Application to Reduce Stress and Promote Wellbeing in University Students

Primary Objective

The National Mental Health Innovation Center (NMHIC) will conduct a trial focused on the utilization and efficacy of the TRIPP VR meditation application as a tool designed to promote wellbeing. The study will evaluate the TRIPP VR meditation application as a novel, non-invasive method to improve wellbeing in a healthy student population. The goal of this project is to better understand the impact of VR mindfulness as an ongoing wellness support for college students. The first aim of the study is to understand factors related to feasibility, acceptability, and overall engagement with TRIPP VR for students. Application usage (e.g., frequency, type of program, duration) and satisfaction will be assessed. The second aim of the study is to investigate the efficacy of TRIPP VR as a wellness support in this population. Perceived stress, mood, mindful awareness, and wellbeing will be assessed across multiple time points. The third aim of the study is to determine whether there are associations between mystical experiences and sense awe related to VR use and the wellness outcomes. We hypothesize that regular use of TRIPP VR, mystical experiences, and awe will be associated with improved wellbeing, mindful awareness, and in-application mood ratings, as well as lower stress.

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Description

Participants will be provided with Oculus Quest or Oculus Quest 2 VR headsets for the duration of the evaluation period (8-weeks) and will be asked to complete at least one 8-10 minute TRIPP VR mindfulness session 3-5 days per week via the VR headset or their mobile phone. Throughout the course of the study, participants will be asked to complete a brief (i.e., four item) standardized stress measure once per week. Outcomes will be assessed at baseline, midline, and endline. All assessments will be completed through Qualtrics and will be sent to participants via an email link. An end-of-study interview or focus group will be completed virtually or in-person with all study participants to assess feasibility, acceptability, and factors related to TRIPP VR that facilitated wellbeing.

Duration of Participation: 8-weeks

Details
Age

18 to 99 years

Eligibility

Students, trainees, and residents at CU Anschutz

Inclusion Criteria. 18+ years of age; willing to wear a VR headset; English speaking; have access to Wi-Fi; enrolled in course(s) or rotation(s) at CU Anschutz at time of consent and for duration of study; have a CU Anschutz or UC Denver email address; based in Colorado for duration of study. Exclusion Criteria. Self-reported clinical-level depression or anxiety; clinical-level post-traumatic stress disorder (PTSD); history of vertigo or dizziness, active nausea or vomiting, history of epilepsy or seizures; inability to use the VR headset or mobile device (e.g., visual impairment); currently pregnant or plans to become pregnant during the duration of the study.

Type of Study

Prevention

Scope

National

Compensation

up to $50

Principal Investigator
Photograph of Chloe Nicksic Sigmon

Chloe Nicksic Sigmon

Study ID

Protocol Number: 21-3622

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