Skip to content

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

Human Performance Evaluation of a Digital Visual Acuity Device: Visual Acuity-001

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06431295
Enrollment
150
Registered
2024-05-28
Start date
2027-10-01
Completion date
2029-06-30
Last updated
2025-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Visual Acuity

Brief summary

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.

Interventions

DEVICEFaceScan

Digital visual acuity device built for iOS (iPhone) that conducts an assessment of visual acuity using a combination of integrated light detection and ranging (LiDAR) and voice processing.

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Number of times the experimental device when measuring visual acuity agreed with standard visual acuity measurementsBaselineNumber of subjects to have agreement between the visual acuity digital device and the clinical assessment

Secondary

MeasureTime frameDescription
Voice samplesBaselineTotal number of voice samples collected of spoken letters

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026