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Patient Performance on Virtual Reality Visual Field Devices as Compared to Standard of Care

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University of Miami

Status

Completed

Conditions

Glaucoma

Treatments

Diagnostic Test: Standard Automated Perimetry
Device: Virtual Reality Visual Field

Study type

Observational

Funder types

Other

Identifiers

NCT04994457
20210472

Details and patient eligibility

About

The purpose of this research is to study the effectiveness and patient experience when measuring visual fields using virtual reality goggles.

Enrollment

287 patients

Sex

All

Ages

1 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion:

  • Any individual who is physically able to take a virtual reality visual field test
  • Patients who either have glaucoma, are glaucoma suspects, or have a strong family history of glaucoma, or have other visual field defects, and normal individual
  • Age: Individuals who are old enough to comprehend the instructions and procedures (1-90)

Exclusion:

  • Adults unable to consent, prisoners
  • Participants who are too tired to take a visual field test
  • Participants who refuse to consent
  • Individuals who are functionally unable to use VRVF

Trial design

287 participants in 6 patient groups

Adults with Glaucoma or Suspected Glaucoma
Description:
Adults with Glaucoma or Suspected Glaucoma, who have previously had standard automated perimetry (SAP) and will receive virtual reality visual field (VRVF) as part of the standard of care
Treatment:
Device: Virtual Reality Visual Field
Visual Field Naive Adults
Description:
Visual Field Naive Adults will receive SAP and VRVF
Treatment:
Device: Virtual Reality Visual Field
Diagnostic Test: Standard Automated Perimetry
Children with Glaucoma or Suspected Glaucoma
Description:
Children with Glaucoma or Suspected Glaucoma, who have previously had SAP and will receive VRVF as part of the standard of care
Treatment:
Device: Virtual Reality Visual Field
Visual Field Naive Children
Description:
Visual Field Naive Children will receive SAP and VRVF
Treatment:
Device: Virtual Reality Visual Field
Diagnostic Test: Standard Automated Perimetry
Remote Care Arm
Description:
Glaucoma or Suspected Glaucoma participants, who have previously had SAP and will receive VRVF at their home
Treatment:
Device: Virtual Reality Visual Field
Ptosis Arm
Description:
Patients diagnosed with Ptosis, brow ptosis, or dermatochalasis, will receive a specialized version of VRVF and SAP, specifically to detect ptosis
Treatment:
Device: Virtual Reality Visual Field
Diagnostic Test: Standard Automated Perimetry

Trial contacts and locations

1

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Central trial contact

Luke Van Leeuwen; Eleonore Savatovsky, MS

Data sourced from clinicaltrials.gov

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