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21. Tyrrell R, Holland K, Dennis D, Wilkins A. Coloured overlays, visual discomfort, visual search and classroom reading. J Res Read. 1995;18(1):10 - 23.
22. Wilkins A J, Jeanes RJ, Pumfrey PD, Laskier M. Rate of Reading Test: its reliability, and its validity in the assessment of the effects of coloured overlays. Ophthalmic Physiol Opt. 1996;16:491–7.
23. Wilkins A, Allen P, Monger L, Gilchrist J. Visual stress and dyslexia for the practicing optometrist. Optom Pract. 2016;17:103–12.
24. Gilchrist JM, Allen PM, Monger L, Srinivasan K, Wilkins A. Precision, reliability and application of the Wilkins Rate of Reading Test. Ophthalmic Physiol Opt. 2021;41:1198–208.
25. Wilkins A, Lewis E, Smith F, Rowland E, Tweedie W. Coloured overlays and their benefit for reading. J Res Read. 2001;24:41–64.
26. Scott L, McWhinnie H, Taylor L, Stevenson N, Irons P, Lewis E, et al. Coloured overlays in schools: Orthoptic and optometric findings. Ophthalmic Physiol Opt. 2002;22:156–65.
27. Allen PM, Dedi S, Kumar D, Patel T, Aloo M, Wilkins AJ. Accommodation, pattern glare, and coloured overlays. Perception. 2012;41:1458–67.
28. Bouldoukian J, Wilkins AJ, Evans BJW. Randomised controlled trial of the effect of coloured overlays on the rate of reading of people with specific learning difficulties. Ophthalmic Physiol Opt. 2002;22(1):55-60.
29. Firth AY, Machin J, Watkins CL. Tilt and reading speed. J AAPOS. 2007;11:52–4.
30. O’Leary CI, Evans BJW. Double-masked randomised placebo-controlled trial of the effect of prismatic corrections on rate of reading and the relationship with symptoms. Ophthalmic Physiol Opt. 2006;26:555–65.
31. O'Leary, C. I., et al. "The effect of low refractive corrections on rate of reading." Optometry in Practice 2014;15(3):87-100.
32. Ousler, G. W., 3rd, et al. "Optimizing Reading Tests for Dry Eye Disease." Cornea 2015;34(8):917-921.
33. Ridder, W. H., et al. "Evaluation of reading speed and contrast sensitivity in dry eye disease." Optom Vis Sci 2013;90(1):37-44.
34. Yammouni, R. and B. J. Evans (2020). "An investigation of low power convex lenses (adds) for eyestrain in the digital age (CLEDA)." J Optom 2020;13(3):198-209.
35. Jang, Y. (2016). "Mobile colored overlay application to Korean WRRT with detailed color control." International Journal of Applied Engineering Research 2016;11(4):2595-2600.
36. Zeri F, Tavazzi S, Punzi M, Miglio F, Evans BJW, De Luca M. New Italian
version of the Wilkins Rate of Reading Test: Materials for repeated­measure designs in optometry and neuropsychological research. Ophthalmic Physiol Opt. 2023;43(4):629-639. doi: 10.1111/opo.13134.
Chapter 6 Coloured filters for visual stress– early studies
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Chapter 7
Do coloured filters work?
Chapter abstract
Research on the use of coloured filters for people with visual stress is described in this chapter. There is a sizeable body of research, and the chapter concentrates on systematic reviews and randomised controlled trials. The use of coloured lenses in those with reading difficulties remains controversial, and reasons for the controversy are discussed. It is argued that it is only in a minority of individuals with reading difficulties (those with visual stress) that the treatment is likely to be successful.
Tinted lenses and coloured lighting
Evidence for the efficacy of tinted lenses prescribed with the Intuitive Colorimeter (Chapter 6) has accumulated over the 25 years since the launch of the system, although there remain unresolved issues. open trial involving patients who responded to reports in the media.3
1 2
The accumulation of evidence began in a small way with an
Open trial
In the open trial, volunteers who responded to an advertisement selected a chromaticity of light that reduced perceptual distortion of text viewed in the Intuitive Colorimeter. Coloured lenses that provided the chosen chromaticity under conventional lighting were then offered to the volunteers (free of charge), and a year later at the end of the trial,
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2024 A. J. Wilkins and B. J. W. Evans, Vision, Reading Difficulties and Visual Stress,
https://doi.org/10.1007/978-3-031-65568-5_7
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more than 80% were still wearing their lenses and reporting benefits. The benefits included greater comfort/clarity when reading (58%) or reduced headaches (47%).3 The trial was suggestive but could not be conclusive because of the role that placebo effects can play in studies of this kind. A double-masked trial that controlled for placebo effects was needed, whereby both patients and clinicians were unaware of whether the patients were wearing a genuine or sham tint. Such a trial was difficult to undertake because patients already knew the colour of the lens they had selected as beneficial.
Double-masked randomised controlled trial (RCT)
In the photograph in Figure 7.1, taken at dusk, the blue of the sky is clearly visible as such and differs from the yellow of the rooms on the left lit with incandescent light, and the white of the room on the right lit with bright fluorescent light. We are not usually aware of these differences in the colour of the illuminating light because we do not see the colours side by side, as in the photo. Instead, everything we see is coloured by the illuminating light and we remain unaware of the colour of the light itself because we adapt to it. This adaptation is a component of the mechanisms of colour constancy – a neural process that enables us to see surface colours as constant despite changes in the spectrum of the light falling on them and consequent changes in the light they reflect.
The process of adaptation permitted the design of a double-masked study4 in which patients were offered coloured lenses without being aware of whether the colour was or was not the colour they had earlier selected as best reducing the distortions of text they perceived. Patients were allowed to adapt to the colour of light that illuminated text in the Intuitive Colorimeter (described in Chapter 6). The processes of adaptation meant that unless the colour was strongly saturated,
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patients had little idea of the colour of the illuminating light. When the light was strongly saturated, patients became aware of the colour but did not usually appreciate that to reproduce this colour under normal room lighting a strongly saturated lens was needed.
Figure 7.1. Window at dusk showing the differences in the colour of
lighting in the sky and in the rooms (incandescent left, fluorescent right).
The colour appearance of the most beneficial lenses (tinted with the optimal colour as selected in the colorimeter) could not therefore be easily recognised. This separation of the colour appearance of tinted lenses from the colour appearance of the coloured light that gave the therapeutic effects permitted a double-masked study to be conducted. Each participant was provided with two pairs of spectacles, only one of which provided the chosen chromaticity (under typical lighting); patients and clinicians were not aware of which pair was which. Additional precautions were taken to ensure that participants could not work out which pair of coloured glasses matched the colour they had chosen in the colorimeter. For example, they never saw the two pairs side by side and there was an interval of at least two weeks after the first pair were sent for retinting before the participant saw the
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second pair of coloured lenses.
Figure 7.2 Double masked study.2 Chromaticities of individual
participants’ active lenses (square points) are connected by a line to the
chromaticites of the control (sham) lenses. The length of the lines
represents the difference in chromaticity between the two. Redrawn from
Wilkins et al.4
The children who participated in the study selected their optimal colour in the Colorimeter using a standard protocol. The protocol involved increasing the saturation to a modest level at a given hue, over the course of about 5 seconds, then waiting about 5 seconds before returning the colour to white. Twelve hues were presented in this way in turn and the good hues shortlisted. At each of the shortlisted hues, the full range of saturation was explored, and the best combination of hue and saturation selected by successive comparison. Hue and saturation were then repeatedly altered in turn by small amounts in order to find the optimal combination of hue and saturation. Having obtained the optimal combination, the hue was gradually changed
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until the child reported the distortions starting to reappear, and this setting provided a suboptimal placebo control. Spectacle lenses were made to match each setting, the chosen setting and the suboptimal placebo setting, and one pair, selected at random by an independent collaborator, was glazed into frames and sent to the child. Figure 7.2 shows a summary of the chromaticities. Of course, the researchers could not be sure the control lens was actually inert, but it was likely that on average the active lenses were more effective than the control. The children and their parents were asked to keep diaries in which they noted any symptoms of eye-strain or headache.
At the end of the investigation, the diaries revealed statistically significantly fewer symptoms when children had been wearing the active tint, see Figure 7.3. The active and placebo tints were closely similar in colour: they differed on average by only 6 times the smallest colour difference that can just be noticed when two coloured surfaces are placed side by side. Therefore, the trial demonstrated not only that the active tint was more beneficial than the control, but also that the tint needed to be selected with precision for optimal effect: similarly coloured lenses did not reduce symptoms as much as the lenses that were precisely tailored to the individual’s needs.
The study included many individuals who did not start the diaries and many who did not complete the study, which was a weakness. However, for those who completed the study there were significantly fewer symptomatic days when the optimal colour was worn than symptomatic days when the sub-optimal colour was worn. This can be seen in Figure 7.3; there are more squares above than below the diagonal. The figure also highlights a second approach to analysing the data. In this type of research, called a crossover study, each participant acts as their own control. The large body of data provided by the daily diaries allowed the researchers to calculate, for each individual
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participant, whether they had statistically significantly fewer symptomatic days with the optimal colour than with the sub-optimal control colour. The solid square symbols indicate the participants for whom there were fewer symptomatic days with the optimal colour than with the sub-optimal, to an extent that is not likely to be attributable to chance (p<0.05). For every case, the benefit was with the optimal and not the sub-optimal colour.
Figure 7.3 Percentage of days when the glasses were worn on which
symptoms of eye-strain or headache occurred. Each point represents a
participant, and the solid points represent participants for whom the
difference in symptoms was individually significant (p<0.05). Redrawn
from Wilkins et al.4
All research studies have their limitations and, as noted above, this study suffered from attrition. This refers to the fact that of the 68 who started the study, 15 did not finish and 16 failed to complete the symptom diary (which was a quite an onerous commitment). It is
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possible that some participants dropped out because they found neither colour beneficial. It seems likely that some dropped out because they found the control colour unhelpful, and this was known to be the case for at least one participant. The problem of attrition means that the researchers may have over-estimated the benefit from coloured filters.
Another limitation is that, during recruitment in the early 1990s, methods of detecting people with visual stress were in their infancy. The Intuitive Overlays and Pattern Glare Test (Chapter 9) had not been invented. In the trial, children were screened with an early set of coloured overlays, which had only a limited range of colours. Participants were included in the study if they chose to use an overlay for at least three weeks. It is now known that this “loose” selection criterion is likely to have included many people who would not meet modern diagnostic criteria. This limitation, in contrast to that caused by attrition, will cause the study to underestimate the benefit from precision tinted lenses. Nowadays, stricter methods are used to detect visual stress (Chapter 10). These methods are more likely to exclude people who will not benefit from precision tinted lenses.
A limitation of all RCTs is that, to control for possible placebo effects, the study will be necessarily undertaken using procedures that depart from normal clinical practice.
5 7
This limits the extent to which the results can be used to predict the effect of an intervention in clinical practice. In the RCT described above, to ensure that participants did not know which tint matched their optimal setting in the colorimeter, no precision tinted trial lenses were used. In clinical practice, as explained in Chapter 9, the optimal chromaticity found in the colorimeter is checked using precision tinted trial lenses under the type(s) of lighting that the patient is most likely to experience. The omission of this stage in the RCT is likely to lead to an underestimation
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of the benefit from precision tinted lenses.
Australian study
Another randomised placebo-controlled trial was conducted by Robinson and Foreman using Irlen lenses.8 Although, the lenses were dispensed some time after the session in which the lenses were selected, patients were able to see their lenses at the time of selection. This means that, depending on participants’ memory skills, the trial may not have been double-masked. Participants were allocated to one of four groups, with at least 34 participants in each group. The first group received the Irlen coloured lens for the entire duration (20 months) of the study. The second group wore a placebo lens for the first 3-4 months and the Irlen lens subsequently. The placebo lens was selected to be a similar colour to the Irlen coloured lens for that individual. The third group wore a “one size fits all” blue lens for the first 3-4 months and the Irlen lens subsequently, and a fourth group wore no lens throughout the 20 months of the study. The Neale Analysis of Reading test was used to measure reading rate, accuracy, and comprehension. The reading assessments took place at the outset of the study, when all four groups were broadly similar, and after 4 months, 8 months and 20 months.
The group that received the Irlen lens at the outset showed a steady increase in reading comprehension which amounted to 4 years in the 20 months of the study. The second group that received the placebo lens and the third group that received the blue lens for the first 3-4 months showed no increase in reading age during this period. Once they received the Irlen lens they showed a rate of increase similar to that of the first group. The groups were not matched for general ability. The differential improvement in reading was only apparent for comprehension, not rate or accuracy.
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ChromaGen study
Harris used tinted contact lenses for people with colour vision defects, arguing that when worn monocularly these improve colour perception. Research indicates that these filters only have a small subjective effect for people with colour vision defects, and should not be worn in occupations that require good colour vision or night vision.9
Harris then extended this approach to individuals with dyslexia, initially monocularly and then binocularly. He used an unconventional method of tint selection, which variously resulted in (1) a coloured lens in one eye only, or (2) different colours in the two eyes, or (3) similar colours in the two eyes. Using clear contact lenses (with only a handling tint) as a control, he showed that in 41 individuals with dyslexia tinted contact lenses improved reading speed on the Wilkins Rate of Reading test to a greater extent than the control.10 Although the study claimed to be a double-masked placebo-controlled trial, it is not certain whether the trial was masked because it seems likely that patients would have been able to appreciate the difference between a contact lens that was tinted and one that was not tinted.
Does the tint need to be precise?
The Wilkins Rate of Reading test (Chapters 6 and 9) was used to examine the precision of colour necessary to improve reading speed. Five patients who routinely wore coloured lenses were asked to read in the Intuitive Colorimeter (without their lenses). The individuals were asked to use the colorimeter to select the colour of light which best improved the clarity and comfort of vision. They were then asked to read passages of text (randomly ordered common words) aloud as quickly as they could under light of different colours, randomly selected on many trials over two sessions.
11 12
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