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Red Light Childhood Myopia Proof-of-concept

What Effect Does Looking At Red Light Have on the Eye in Children and Young People? - a Proof-of-concept Study

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06771258
Enrollment
24
Registered
2025-01-13
Start date
2025-02-01
Completion date
2026-02-01
Last updated
2025-01-13

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

Conditions

Myopia

Brief summary

In this project the research team will begin to find out whether shining a red LED light at the eyes can slow down the worsening of short-sightedness in children. This is important, because short-sightedness now starts at a younger age and worsens faster than in the past. Many people are at risk of permanently losing their eyesight in middle-age because of short-sightedness. The researchers plan to use red LED light, which is safe to use. Red-light treatment improves the blood flow at the back of the eye, in a layer called choroid, which can be measured on eye-scans. The team have done a study with healthy adults, which showed that red-light is safe and gently improves the blood flow at the back of the eye. In adults, this has no effect on myopia, because their eyes are fully grown. In children, red-light may slow down myopia, and in this project, the researchers want to find out which level of red-light is needed to have this effect. The researchers will ask 24 children age 5-12 years to use red-light for three minutes twice a day for three months. Three will be 4 groups of children, and each group will use a different level of brightness. The researchers will measure the eye length and the thickness of the choroid at the start and 1 and 3 months later and compare the change in eye length between the different groups. In practice, children will need to use the treatment for several years. The researchers will use the results of this study to prepare a longer study with more children.

Interventions

Red LED light

Sponsors

University College, London
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* short-sightedness between -1.00D and -6.00 diopters in both eyes * best-corrected visual acuity 0.1 logMAR or better in both eyes

Exclusion criteria

* underlying condition/syndrome causing myopia * previous or current myopia-modifying treatment * abnormal ocular refractive anatomy or previous intraocular or ocular surgery

Design outcomes

Primary

MeasureTime frameDescription
Axial length3 monthsThe researchers will measure the length of the eyeballs using an optical biometer; these are the most sensitive outcome measure in myopia studies, and the least invasive measurement method.

Secondary

MeasureTime frameDescription
Spherical equivalent3 monthsThe team will measure the refractive error (prescription for spectacles) using an open-view autorefractor, as a secondary measure of myopia progression.
Subfoveal choroidal thickness3 monthsThe team will acquire an optical coherence tomography scan. On the scan, the researchers will measure the choroidal thickness, which is frequently used as a proxy measure of the treatment effect of interventions to slow myopia progression. The choroid is a vascular layer underneath the retina at the back of the eye.
Colour contrast sensitivity3 monthsAs a safety measure, the researchers will measure colour contrast sensitivity on a computer-screen, showing participants coloured symbols on a grey background. This is the most sensitive test for photoreceptor health, the layer of cells in the retina which change light signals to electrical signals.
Visual acuity3 monthsAs a secondary safety outcome, the researchers will measure the participant's visual acuity, using a test where participants read letters of reducing size on a chart.
Tolerability/usability3 monthsThe researchers will ask participants open-ended questions about their thoughts and experience with using red-light treatment, and about easier ways for children to use it.

Countries

United Kingdom

Contacts

Primary ContactAnnegret Dahlmann-Noor, PhD
anngret.dahlmann@ucl.ac.uk020 7253 3411

Outcome results

None listed

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