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

ConditionVisual Acuity
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMayo Clinic

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adult patients (≥ 18 years) who come to Ophthalmology Clinic.

Willing and able to provide consent.

Disqualifiers

Individuals < 18 years of age.

Unable to provide consent.

Trial design

Design model

Single group

Treatments tested in this trial

  • FaceScan

    Device

    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.

Treatment groups

150 Participants
are divided into 1 treatment group
Group A: Digital Visual Acuity TestExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Number of times the experimental device when measuring visual acuity agreed with standard visual acuity measurements

Number of subjects to have agreement between the visual acuity digital device and the clinical assessment

Time frame
Baseline

Secondary outcomes

1

Voice samples

Total number of voice samples collected of spoken letters

Time frame
Baseline

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: