Evidence map›Paper›PMID 37589437›Full record

ArticleOphthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists)2023

Rapid measurement and machine learning classification of colour vision deficiency.

Jingyi He, Peter J Bex, Jan Skerswetat

Open access · hybridAbstract read
In one paragraph

Article in Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Application of the angular indication measurement and foraging interactive D-prime paradigms to tablet-based color vision testing.Journal of the Optical Society of America. A, Optics, image science, and vision · 2025
    Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Jingyi HeDepartment of Psychology, Northeastern University, Boston, Massachusetts, USA.ORCID 0000-0001-6100-6367
Peter J BexDepartment of Psychology, Northeastern University, Boston, Massachusetts, USA.
Jan SkerswetatDepartment of Psychology, Northeastern University, Boston, Massachusetts, USA.ORCID 0000-0002-2470-8404
Northeastern University · US

Funding

ARBi - Assessment and Rehabilitation of Binocular Sensorimotor DisordersR01EY032162 · NEI · NORTHEASTERN UNIVERSITY · PI Peter John Bex, David G HUNTER · 2022 to 2026
$2.4M
Eye Movement Rehabilitation in Low Vision PatientsR01EY029713 · NEI · NORTHEASTERN UNIVERSITY · PI BEX, PETER JOHN · 2019 to 2023
$1.9M
NEI NIH HHS R01 EY029713NEI NIH HHS R01 EY032162NIH HHS R01 EY029713
6 · The paper itself

Abstract

Colour vision deficiencies (CVDs) indicate potential genetic variations and can be important biomarkers of acquired impairment in many neuro-ophthalmic diseases. However, CVDs are typically measured with tests which possess high sensitivity for detecting the presence of a CVD but do not quantify its type or severity. In this study, we introduce Foraging Interactive D-prime (FInD), a novel computer-based, generalisable, rapid, self-administered vision assessment tool and apply it to colour vision testing. This signal detection theory-based adaptive paradigm computed test stimulus intensity from d-prime analysis. Stimuli were chromatic Gaussian blobs in dynamic luminance noise, and participants clicked on cells that contained chromatic blobs (detection) or blob pairs of differing colours (discrimination). Sensitivity and repeatability of FInD colour tasks were compared against the Hardy-Rand-Rittler and the Farnsworth-Munsell 100 hue tests in 19 colour-normal and 18 inherited colour-atypical, age-matched observers. Rayleigh colour match was also completed. Detection and discrimination thresholds were higher for atypical than for typical observers, with selective threshold elevations corresponding to unique CVD types. Classifications of CVD type and severity via unsupervised machine learning confirmed functional subtypes. FInD tasks reliably detect inherited CVDs, and may serve as valuable tools in basic and clinical colour vision science.

Indexed as

Cardiovascular DiseasesColor VisionColor Vision DefectsColor PerceptionHumansMachine LearningVision Testscolour detectioncolour discriminationcolour vision deficiencycone-isolating directionsk-means clusteringunsupervised machine learningvision diagnostics

Identifiers

PMID37589437
PMCPMC10592291
OpenAlexW4385898158

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.