Choroidal Changes Post Short Term Exposure To Virtual Reality Devices
Not Applicable
Withdrawn
- Conditions
- Myopia
- Interventions
- Device: Visu
- Registration Number
- NCT04140877
- Lead Sponsor
- Visu, Inc.
- Brief Summary
This is a prospective, randomized, controlled, contralateral eye, clinical study. The objective of the study is to determine the impact of Virtual Reality (VR) usage on choroidal thickness when viewed through a test display compared to a control (standard) VR display. The hypothesis is that there will be less choroidal thinning in the eye viewing the test VR screen compared to the eye viewing the control VR screen.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- Is at least 13 years of age and has full legal capacity to volunteer;
- Has read and signed an information consent letter;
- Visual Acuity of +0.20 logMAR or better in each eye;
- Is willing and able to follow instructions and maintain the appointment schedule.
Key
Exclusion Criteria
- Is participating in any concurrent clinical or research study;
- Has any known active ocular disease and/or infection;
- Has a systemic condition that in the opinion of the investigator may affect a study outcome variable;
- Is amblyopic in either eye;
- Has a colour vision abnormality;
- Commonly experiences motion sickness.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Visu OD, Control OS Visu Contralateral eye study Control OD, Visu OS Visu Contralateral eye study
- Primary Outcome Measures
Name Time Method Choroidal thickness 2 hours
- Secondary Outcome Measures
Name Time Method Axial length 3 months Choroidal thickness 3 months