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      ColourSpot, a novel gamified tablet-based test for accurate diagnosis of color vision deficiency in young children

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          Abstract

          There is a need for a straightforward, accessible and accurate pediatric test for color vision deficiency (CVD). We present and evaluate ColourSpot, a self-administered, gamified and color calibrated tablet-based app, which diagnoses CVD from age 4. Children tap colored targets with saturations that are altered adaptively along the three dichromatic confusion lines. Two cohorts (Total, N = 772; Discovery, N = 236; Validation, N = 536) of 4–7-year-old boys were screened using the Ishihara test for Unlettered Persons and the Neitz Test of Color Vision. ColourSpot was evaluated by testing any child who made an error on the Ishihara Unlettered test alongside a randomly selected control group who made no errors. Psychometric functions were fit to the data and “threshold ratios” were calculated as the ratio of tritan to protan or deutan thresholds. Based on the threshold ratios derived using an optimal fitting procedure that best categorized children in the discovery cohort, ColourSpot showed a sensitivity of 1.00 and a specificity of 0.97 for classifying CVD against the Ishihara Unlettered in the independent validation cohort. ColourSpot was also able to categorize individuals with ambiguous results on the Ishihara Unlettered. Compared to the Ishihara Unlettered, the Neitz Test generated an unacceptably high level of false positives. ColourSpot is an accurate test for CVD, which could be used by anyone to diagnose CVD in children from the start of their education. ColourSpot could also have a wider impact: its interface could be adapted for measuring other aspects of children’s visual performance.

          Supplementary Information

          The online version contains supplementary material available at 10.3758/s13428-021-01622-5.

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          Chromaticity diagram showing cone excitation by stimuli of equal luminance.

          In a space where Cartesian coordinates represent the excitations of the three cone types involved in color vision, a plane of constant luminance provides a chromaticity diagram in which excitation of each cone type (at constant luminance) is represented by a linear scale (horizontal or vertical), and in which the center-of-gravity rule applies with weights proportional to luminance.
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            Worldwide prevalence of red-green color deficiency.

            Literature that describes the prevalence of inherited red-green color deficiency in different populations is reviewed. Large random population surveys show that the prevalence of deficiency in European Caucasians is about 8% in men and about 0.4% in women and between 4% and 6.5% in men of Chinese and Japanese ethnicity. However, the male: female prevalence ratio is markedly different in Europeans and Asians. Recent surveys suggest that the prevalence is rising in men of African ethnicity and in geographic areas that have been settled by incoming migrants. It is proposed that founder events and genetic drift, rather than natural selection, are the cause of these differences.
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              Luminance noise and the rapid determination of discrimination ellipses in colour deficiency.

              A computer-controlled test of colour vision is described, in which luminance noise and masking contours are used to ensure that the subject's responses depend on chromatic signals. The test avoids the need--common to most computer-controlled tests--to define equiluminance for the individual subject before the colour test itself can be administered. The test achieves a good separation of protan and deutan subjects and reveals the large range of chromatic sensibilities among anomalous trichromats. As a population, dichromats had higher thresholds on the tritan axis of the test than did normals. In an extension of the test, full discrimination ellipses were measured for normal and colour-deficient observers. The nature of anomalous trichromacy is discussed and the possibility is raised that hybrid genes, resulting from genetic recombination, may code for incorrectly labelled or functionally impaired molecules.
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                Author and article information

                Contributors
                Anna.Franklin@sussex.ac.uk
                J.Bosten@sussex.ac.uk
                Journal
                Behav Res Methods
                Behav Res Methods
                Behavior Research Methods
                Springer US (New York )
                1554-351X
                1554-3528
                31 August 2021
                31 August 2021
                2022
                : 54
                : 3
                : 1148-1160
                Affiliations
                [1 ]GRID grid.12082.39, ISNI 0000 0004 1936 7590, The Sussex Colour Group, School of Psychology, , University of Sussex, ; Falmer, Brighton, BN1 9QH UK
                [2 ]GRID grid.4795.f, ISNI 0000 0001 2157 7667, Facultad de Psicología, , Universidad Complutense de Madrid, ; Pozuelo de Alarcón, Madrid 28883 Spain
                [3 ]GRID grid.12082.39, ISNI 0000 0004 1936 7590, School of Psychology, , University of Sussex, ; Falmer, Brighton, BN1 9QH UK
                [4 ]GRID grid.12082.39, ISNI 0000 0004 1936 7590, Sussex Vision Lab, School of Psychology, , University of Sussex, ; Falmer, Brighton, BN1 9QH UK
                Author information
                http://orcid.org/0000-0003-2065-7491
                Article
                1622
                10.3758/s13428-021-01622-5
                9170621
                34463952
                c60dd2fc-ad7d-4816-8d0e-e4041c567314
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 14 May 2021
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                © The Psychonomic Society, Inc. 2022

                Clinical Psychology & Psychiatry
                color vision deficiency,visual development,mobile health applications,pediatric,gamification

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