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Clinical evaluation of a novel automated visual acuity and contrast sensitivity tests using augmented reality glasses

Recruiting
Conditions
ormal vision subjects and mild, or moderate visual impairment patients.
Visual acuity test, Contrast sensitivity test, Augmented reality glasses
Registration Number
TCTR20240401008
Lead Sponsor
Charturong Tantibundhit
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
200
Inclusion Criteria

1. Age 18 years and above, 2. VA measured by the ETDRS chart is equal or worse than 20/20 and equal or better than 20/200

Exclusion Criteria

1. A history of significant motion sickness, active nausea, and vomiting or epilepsy, 2. Facial or head deformity (e.g., a history of brain or facial surgery), 3. Unable to use clicker (e.g., Hand movement disorders or global movement disorders), 4. Ptosis and dermatochalasis, 5. Dementia, 6. Patients who have electronic device implantation (e.g., cardiac pacemakers, hearing aids and defibrillators)

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual acuity measured by Rokid Max Augmented reality glasses at the beginning of study a pixel (of the Rokid Max Augmented reality glasses display) unit ,Visual acuity measured by ETDRS chart at the beginning of study a log MAR unit ,Contrast sensitivity measured by Rokid Max Augmented reality glasses at the beginning of study a unit of logCS (Contrast sensitivity),Contrast sensitivity measured by the Mars CS test at the beginning of study a unit of logCS (Contrast sensitivity)
Secondary Outcome Measures
NameTimeMethod
Test time of VA and CS testing by Rokid Max Augemented reality glasses at the end of the test (around at 1 minute) seconds
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