Status:

COMPLETED

Study to Identify if OVR Health's VR-Kit is Safe to Use and Helps to Improve Focus, Attention and Reduce Worry & Rumination.

Lead Sponsor:

Oxford VR

Collaborating Sponsors:

Citruslabs

Conditions:

Anxiety

Depression, Anxiety

Eligibility:

All Genders

18-79 years

Phase:

NA

Brief Summary

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 ...

Eligibility Criteria

Inclusion

  • Male or female over 18 years old
  • Must be in good general health
  • Self-reported with the following symptoms (as assessed by questions and questionnaires in study material):
  • Finding it hard to let go of difficult thoughts.
  • Looking out for signs of a potential threat in their environment (or in their body) that unhelpfully maintains their problem.
  • Engaging in repetitive, unhelpful patterns of negative thinking (worry \& rumination). • These may be due to a diagnosis of a mental health condition, but this is not required for entry into the study.
  • Good understanding of written and spoken English
  • Willing and able to give informed consent
  • Willing and able to follow the study protocol
  • Willing and able to use VR headset at home
  • WiFi connection to connect VR headset at home
  • Willing and able to return VR headset

Exclusion

  • Current diagnosis of epilepsy, dementia, or another neurological disease that may prevent the use of VR hardware and software
  • Individuals with suicidal or self-harm thoughts
  • Significant visual, auditory, or balance impairment
  • Insufficient comprehension of English
  • Primary diagnosis of alcohol or substance abuse disorder, or personality disorder • Significant learning disability
  • Current active suicidal plans or self-harm (in which case participant will be referred to appropriate crisis service)
  • Receiving current alternative psychotherapy treatment
  • Unwilling to provide consent
  • Unwilling to follow the study protocol

Key Trial Info

Start Date :

February 15 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 15 2021

Estimated Enrollment :

90 Patients enrolled

Trial Details

Trial ID

NCT05291429

Start Date

February 15 2021

End Date

July 15 2021

Last Update

March 22 2022

Active Locations (1)

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Citruslabs

Santa Monica, California, United States, 90404