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Development and Validation of an Automated Self-administered Visual Acuity System

Development and Validation of an Automated Self-administered Visual Acuity System

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06540001
Acronym
AutoVA
Enrollment
100
Registered
2024-08-06
Start date
2024-08-01
Completion date
2025-08-01
Last updated
2024-08-06

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

Conditions

Visual Impairment

Keywords

Visual acuity

Brief summary

Visual acuity tests, commonly conducted in clinics and used for health screenings, are becoming more in demand due to an aging population. Current online self-eye check apps are limited as they don't accurately reflect true distance vision assessed in clinical settings. These tests, performed by trained personnel, are time-consuming and can cause delays in clinics. This project aims to develop an automated Visual Acuity (VA) station using AI technologies like speech-to-text and computer vision, hypothesizing that it can match the accuracy of manual assessments by clinic staff, thus potentially reducing waiting times and improving efficiency.

Detailed description

Visual acuity is done as a routine eye check for the majority of eye patients in the clinic. It is also done as a screening test for pre-employment health checks and health screening. Patients can be checked for refractive errors, on a community level or screened for eye diseases, for those with chronic medical conditions. With the increasing burden of aging population and eye conditions, the number of patients in eye clinics will increase. There are a few existing online applications that allow self-eye checks, however there are limitations. They are usually done at an intermediate distance, i.e. distance from phone to eye and does not accurately represent true distance vision. Distance vision is typically set at 4- 6m in a clinical setting. A visual acuity test is administered by specially trained healthcare personnel, such as optometrists and patient service assistants, which is often time-consuming and labour intensive, where one-on-one attention is required. In addition, vision is subjective and re-testing may be required at times to ensure accurate vision assessment. As the visual acuity test is the first clinical station patient goes to after registration, this leads to a bottleneck in workflow causes delays in the subsequent services and eventually increases patient waiting times in the clinics. This project aims to develop and validate an automated Visual Acuity (VA) station through speech-to-text and computer vision technology in comparison to existing manual VA assessments. We hypothesize that we are able to use artificial intelligence to understand patient's speech and posture to automate the visual acuity test. We also hypothesize that the automated visual acuity test is comparable to having VA checked manually by a clinic staff.

Interventions

DEVICEAutomated visual acuity

The automated visual acuity device is developed in collaboration with Tan Tock Seng Hospital, Singapore Institute of Technology and Nanyang Technological University. It uses artificial intelligence for pose estimation and speech recognition to infer if the participant is reading the correct letters displayed on the screen.

Sponsors

Singapore Institute of Technology
CollaboratorOTHER
Nanyang Technological University
CollaboratorOTHER
Lee Kong Chian School of Medicine, Nanyang Technological University
CollaboratorUNKNOWN
Tan Tock Seng Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patients age >21 and able to give consent 2. Patients who have at least counting finger vision 3. Patients who is able to speak in an audible and clear voice 4. Patients who is able to use a digital device independently (e.g. handphone)

Exclusion criteria

1. Patients on wheelchair/ walking aids 2. Patients with hearing difficulties 3. Patients with speech difficulties 4. Patients who have cognitive impairment 5. Patients who are hemiplegic/ motor dysfunction 6. Patients who have vision worse than counting fingers 7. Patients who are pregnant

Design outcomes

Primary

MeasureTime frameDescription
Best corrected visual acuity with and without pinhole using Snellen letters and numbers1 yearBest corrected visual acuity will be expressed in metres (e.g. 6/6-1), and will be converted to LogMAR for analysis.

Contacts

Primary ContactKelvin Z Li., MBBS, MTech, FRCOphth
contact@ttsh.com.sg+6562566011

Outcome results

None listed

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