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Not Yet RecruitingNCT07108556

Brief Mindfulness Workshop With or Without Virtual Reality: A Pilot Study

Brief Mindfulness Workshop With or Without Virtual Reality: A Randomized Crossover Design

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
144 (estimated)
Sponsor
The University of Hong Kong · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The current study uses a randomized cross-over design, in which participants are exposed to brief mindfulness-based experiential sessions with and without incorporating virtual reality (i.e., the experimental and control conditions, respectively). Order of exposure to these two conditions are counter-balanced and participants are randomized into the two arms of exposure in a different order. Furthermore, this study includes the use of both subjective self-report and objective physiological measures of mental wellbeing. It is hypothesized that VR-incorporated mindfulness-based experiential session brings a greater improvement in state mindfulness, state affect, and stress response. Results shed light on the added value of incorporating VR into brief MBIs, particularly in reference to the typical practice of promoting mindfulness in the local community.

Conditions

Interventions

TypeNameDescription
BEHAVIORALMindfulness VR-TypicalParticipants first experience mindfulness exercise with virtual reality incorporated, then another mindfulness exercise with only audio-guidance as typically delivered without the technology
BEHAVIORALMindfulness Typical-VRParticipants first experience mindfulness exercise with only audio-guidance, then another mindfulness exercise with virtual reality incorporated

Timeline

Start date
2025-08-02
Primary completion
2025-12-31
Completion
2025-12-31
First posted
2025-08-07
Last updated
2025-08-07

Locations

1 site across 1 country: Hong Kong

Source: ClinicalTrials.gov record NCT07108556. Inclusion in this directory is not an endorsement.

Brief Mindfulness Workshop With or Without Virtual Reality: A Pilot Study (NCT07108556) · Clinical Trials Directory