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Next Generation Home Vision Assessment

Next Generation Home Vision Assessment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06428435
Acronym
NGHVA
Enrollment
206
Registered
2024-05-24
Start date
2023-03-01
Completion date
2024-12-31
Last updated
2025-07-18

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

Conditions

Amblyopia, Pediatric Disorder, Vision; Low, One Eye (Other Eye Normal)

Keywords

teleophthalmology, remote consultations, amblyopia, paediatrics, telemedicine, digital health

Brief summary

Comparison of live remote paediatric digital vision testing outcomes versus face to face appointments in orthoptic clinic

Detailed description

Study Overview The Next Generation Home Vision Assessment study aims to evaluate the feasibility and accuracy of conducting vision assessments at home using a web-based platform. This prospective, non-interventional, multi-center study will compare home-based vision tests with traditional hospital-based assessments. Study Background The COVID-19 pandemic has significantly limited patients' ability to attend in-person eye clinic appointments, impacting vision assessments and management. Ramifications in delays continue to have an impact. Study Rationale This study seeks to validate home-based vision assessments against standard in-person evaluations to ensure patients can be effectively monitored and managed remotely. The use of a web-based platform for vision tests could offer a reliable alternative, reducing hospital visits and maintaining care standards. Objectives and Endpoints Primary Objective: To compare the accuracy of home-based visual acuity tests to hospital-based assessments. Secondary Objectives: To evaluate other aspects of visual function (e.g., visual fields, color vision, contrast sensitivity) and measure patient engagement and test duration. Study Design Type: Prospective, non-interventional Participants: Adults and children attending hospital eye services Sample Size: 360 completed assessments Duration: Minimum of 6 months Study Procedure Participants attending hospital eye services will be recruited and provided with a patient information leaflet. Those willing to participate will undergo a visual acuity test +/- additional vision tests (secondary outcomes) during a video consultation. Hospital-based assessment results will be compared to home-based test results to determine accuracy.

Interventions

DIAGNOSTIC_TESTVision Test

Remote vision testing via digital screen

Sponsors

Birmingham Children's Hospital
CollaboratorOTHER
NHS Fife
CollaboratorOTHER_GOV
NHS Highland
CollaboratorOTHER
NHS Forth Valley
Lead SponsorOTHER_GOV

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Months to 90 Years
Healthy volunteers
No

Inclusion criteria

\- Patients attending hospital eye services will be eligible for enrolment. Age: less than 90 years old English speakers, as no available resource for translation services. Parents / patients must be able to provide consent Patient must be able to communicate what he / she sees on a vision assessment chart. Must have access to smartphone, tablet or home computer that can run video conferencing platforms.

Exclusion criteria

Non English speakers or lack of ability to consent Inability to communicate what is seen on a chart, or inability to complete a preferential looking visual acuity test Inability to connect to a video conferencing platform.

Design outcomes

Primary

MeasureTime frameDescription
Acuity2 weeksHome versus Remote Acuity difference

Secondary

MeasureTime frameDescription
Colour Vision2 weeksDigital versus in clinic standard
Visual field2 weeksDigital versus in clinic standard

Countries

United Kingdom

Outcome results

None listed

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