This is a randomized-controlled interventional treatment study with three arms of comparable demographics to evaluate the safety and efficacy of OVR Health's VR experience to improve control over the focus of attention and reduce worry and rumination in individuals who have reported problems with these issues.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
90
Virtual reality experience
Citruslabs
Santa Monica, California, United States
Safety of virtual reality device and reduction in worry and rumination (PHQ9)
Changes in perceived safety using the PHQ9 questionnaire (Scale 0-3).
Time frame: 5 weeks
Safety of virtual reality device and reduction in worry and rumination (Perseverative Thinking score )
Changes in perceived safety using the Perseverative Thinking score (Scale 0-4).
Time frame: 5 weeks
Impact of coaching on virtual reality intervention effectiveness (PHQ9)
Changes in the PHQ9 questionnaire (0-3) in comparison to Group 2 (no coaching) and placebo arm (no intervention) with a lower score showing fewer symptoms.
Time frame: 5 weeks
Impact of coaching on virtual reality intervention effectiveness (Perseverative Thinking scor)
Changes in the Perseverative Thinking score (0-4) in comparison to Group 2 (no coaching) and placebo arm (no intervention) with a lower score showing fewer symptoms.
Time frame: 5 weeks
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