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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Abigail Orr, BSc 020 7188 4885
eyeresearch@gstt.nhs.uk


Study Location:

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Be Part of Research - Trial Details - Developing Better Computerised Vision Tests (CVTV)

Developing Better Computerised Vision Tests (CVTV)

Recruiting

Open to: ALL

Age: 3.0 - 99.0

Medical Conditions

Amblyopia
Vision Disorders
Vision, Low
Macular Degeneration


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Clinical vision measurements usually involve printed charts with an eye care professional interpreting patient responses to generate a score. Those scores determine the need for or outcome of treatment. Detecting change can be improved with strict procedures/scoring, lending itself to computerisation. This in turn allows integration with electronic medical records. Many eye tests could be computerised in this way. At Guys and St Thomas' NHS Foundation Trust, the investigators have developed and validated a computerised test of distance visual acuity, called COMPlog which is now in widespread use. The investigators now want to increase the range of tests available.

There is also a need to longitudinally monitor for adverse change. Such monitoring must be developed to keep false positive and false negative change detection to a minimum.

The aims of this two year linked program are to:

Part A) validate an extended range of computerised vision measurement tests against their gold standard hard copy printed equivalents. Some of these tests are designed for use in children and all are meant to quantify both normal and impaired vision. Patients of all ages and visual function will therefore be recruited from St Thomas' Hospital. The specific tests we aim to validate are logMAR Letter Near Acuity, Word Near Acuity, Letter Contrast Sensitivity, Auckland Optotypes Picture Acuity, Low Contrast Letter Acuity, Stereoacuity and Vanishing Optotypes. Patients will undergo test-retest measurements with up to two of these.

Part B) Iteratively develop an application for use in home monitoring of subjects at risk of treatable vision loss due to age related macular degeneration.

All computerised tests in parts A and B will be performed on prototype software. Eye patients will be recruited as subjects. Patients recruited to part A will undergo tests on one day for up to an hour, subjects in part B will participate for between 1 hour and two months.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Apr 2024 Jan 2025

OBSERVATIONAL

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : Comparison of gold standard printed tests and computerised versions

Intervention Arm Group : Near logMAR letter acuity;

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : Comparison of gold standard printed tests and computerised versions

Intervention Arm Group : Near logMAR word acuity;

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : Comparison of gold standard printed tests and computerised versions

Intervention Arm Group : Red Green Stereoacuity;

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : Comparison of gold standard printed tests and computerised versions

Intervention Arm Group : Auckland Optotypes/Auckland Vanishing Optotypes;

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : Comparison of gold standard printed tests and computerised versions

Intervention Arm Group : Vanishing Optotype Sloan letters;

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : Comparison of gold standard printed tests and computerised versions

Intervention Arm Group : Letter Contrast Sensitivity;

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : Comparison of gold standard printed tests and computerised versions

Intervention Arm Group : Low contrast letter acuity;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • St Thomas' Hospital NHS Foundation Trust
    London


The study is sponsored by Guy's and St Thomas' NHS Foundation Trust and is in collaboration with King's College London.




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Read full details for Trial ID: NCT06224751
Last updated 15 March 2024

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