Skip to content

Reading; Through the Eyes of a University Student

Reading; Through the Eyes of a University Student. A Double-masked, Randomised Control Trial to Assess the Effect of Precision Tinted Spectacle Filters on Visual Stress Symptoms Within the University Student Population

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04318106
Enrollment
72
Registered
2020-03-23
Start date
2020-01-27
Completion date
2025-06-30
Last updated
2026-02-19

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

Conditions

Meares-Irlen Syndrome, Reading Difficulties, Visual Stress

Keywords

Visual stress, Meares-Irlen syndrome, reading difficulties

Brief summary

This is a double-masked randomized controlled trial which aims to assess the effects of precision tinted spectacle lenses on visual stress symptoms within an undergraduate University student population.

Detailed description

The participants will be recruited from the undergraduate Ulster University student population. Those students who have been identified as potentially having visual stress will be invited to undergo screening tests to assess their eligibility to participate in the randomized controlled trial. Visit 1: Each consenting participant will undergo tests to assess their eligibility to participate in this study. Provided the participant meets the inclusion criteria then they will undergo a baseline eye examination and reading tests including the Wilkins Rate of Reading test (WRRT). The participant will then undergo colorimetry testing using the Intuitive colorimeter (Cerium TM) using the established procedure to individually measure the optimum chromaticity which alleviates visual stress symptoms for each participant. This will be the 'experimental' colour. A second colour will be measured at which visual stress symptoms will be present, this colour will not be aversive to the participant and will be as close to the 'experimental' colour as possible to aid masking. This will be the 'control' colour and it will be individually determined for each participant. Participants and researchers will be masked to which spectacles are 'control' and 'experimental' throughout the course of the trial. Visit 2 & 3: The participant will be invited to return to collect one pair of spectacle with coloured lenses. Reading speed will be assessed using the Wilkins Rate of Reading Test (WRRT) and visual stress will be assessed using a symptom questionnaire and Pattern Glare Test (PGT) with and without the coloured spectacles. The participant will be asked to take the spectacles away and will be advised to wear the spectacles for concentrated tasks, including reading. The participant is free to choose when they wish to wear the spectacles. The participant will keep the spectacles for a minimum of six weeks, after this time they will be invited to return the spectacles and repeat measures of reading speed and visual stress will be assessed. Participants will be asked to document reading symptoms in an online diary and note the length of spectacle wear-time at the start and end of the 6-week wear period. There will be a time lapse between visit 3 and visit 4 where the participant will have no coloured spectacles. Visit 4 & 5 The participant will return to collect the other pair of spectacles. Reading speed and visual stress will be assessed as in visit 2 & 3. They will keep the spectacles for the same time period. They will be invited to return, at the end of visit 5 the participant will be able to chose their preferred pair of coloured spectacles to take away with them to keep. Three months later the participant will be contacted to check if they are still wearing the coloured spectacles.

Interventions

DEVICEPrecision tinted spectacle lenses

Precision tinted spectacles lenses (Cerium Technologies TM)

Sponsors

University of Ulster
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

The researcher will perform colorimetry testing to measure the chromaticity of the 'experimental' and 'control' coloured lenses.The 'experimental' and 'control' colour will be as similar in chromaticity as possible. The details of the 'experimental' and 'control' colour will be given to an external person who will randomly assign the order in which the spectacles will be collected by the participant. There is a significant time lapse between the colorimetry assessment where the 'experimental' and 'control' colours are measured and the collection of the first pair of spectacles.

Intervention model description

The participant will be given either the 'experimental' coloured spectacle lenses or the 'control' coloured spectacle lenses to wear for a minimum of ten weeks, the spectacles will be returned. A 'washout' period will occur and then the participant will be given the alternative pair of coloured spectacles to wear.

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* All consenting undergraduate University students, studying at Ulster University who have visual stress symptoms.

Exclusion criteria

* Reduced visual acuity * Uncorrected spectacle prescription * Decompensating heterophoria * Heterotropia * Accommodative insufficiency * Convergence insufficiency * Ocular health abnormality * Any participant currently using precision tinted lenses

Design outcomes

Primary

MeasureTime frameDescription
Reading rate12 weeksWilkins rate of reading test
Symptoms12 weeksSymptom diary to be completed by the participant daily for the first and final week of wear of each pair of spectacles. The participant will be asked details about how much reading they have performed, how long they have worn the spectacles for and if they have experienced any symptoms of visual perceptual distortions.

Secondary

MeasureTime frameDescription
Voluntary use of coloured spectacles3 monthsUnprompted, voluntary use of the 'experimental' coloured spectacles

Countries

United Kingdom

Contacts

PRINCIPAL_INVESTIGATORSara McCullough, PhD

Ulster University

STUDY_DIRECTORJulie-Anne Little, PhD

Ulster University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026