Evaluation of a Digital Visual Acuity Device vs. Standard Visual Acuity Measurements

Mayo Clinic

Status: Begins enrollment in a year or more

Conditions: Visual Acuity

Treatments: Device: FaceScan

Study type: Interventional

Funder types: Other

Identifiers

NCT06431295

23-007148

Details and patient eligibility

About

The purpose of this research is to validate and determine the accuracy of the experimental device when measuring visual acuity versus our standard visual acuity measurements and to gather voice recordings of letters to help build a special system that recognizes spoken letters.

Enrollment: 150 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Adult patients (≥ 18 years) who come to Ophthalmology Clinic.
• Willing and able to provide consent.

Exclusion criteria

• Individuals < 18 years of age.
• Unable to provide consent.

Trial design

Primary purpose: Screening

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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150 participants in 1 patient group

Digital Visual Acuity Test

Experimental group

Description:

Subjects for an ophthalmological examination that includes a visual acuity examination at Mayo Clinic in Florida have a digital visual acuity test conducted with the FaceScan device.

Treatment:

Device: FaceScan