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The effect of a virtual three-dimensional eye model on patient satisfaction and understanding: a randomised control trial

The effect of a virtual three-dimensional eye model on patient satisfaction and understanding: a randomised control trial

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624001153505
Acronym
ORE (One Right Eye)
Enrollment
92
Registered
2024-09-23
Start date
2023-05-22
Completion date
2023-11-14
Last updated
2024-09-30

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

Conditions

None listed

Brief summary

A single-centre, open-label, randomised controlled trial to investigate whether the use of a virtual three-dimensional interactive eye model (One Right Eye model) during a standard outpatient public ophthalmology clinic affects overall patient satisfaction with their appointment, understanding of their ophthalmic condition, and rating of their doctor’s explanation.

Interventions

Intervention = a standard ophthalmic consultation assisted by an interactive virtual three-dimensional eye model (One Right Eye) on the doctor’s computer. The One Right Eye (ORE) is a virtual, interactive, three-dimensional model of the right human eye that can be loaded on any smart device with internet access (onerighteye.com). The model uses innovative digital tools to create a detailed, immersive simulation of common eye conditions and how they progress. The use of the virtual eye model duri

Intervention = a standard ophthalmic consultation assisted by an interactive virtual three-dimensional eye model (One Right Eye) on the doctor’s computer. The One Right Eye (ORE) is a virtual, interactive, three-dimensional model of the right human eye that can be loaded on any smart device with internet access (onerighteye.com). The model uses innovative digital tools to create a detailed, immersive simulation of common eye conditions and how they progress. The use of the virtual eye model during the consult is at the doctor's discretion.

Sponsors

Ophthalmology Department, The Royal Melbourne Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

All adult patients presenting to a public ophthalmology clinic (except for injection clinics).

Exclusion criteria

- Declining to participate - Legally blind - Cognitively impaired - Primary language other than English

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026