Altered Non-Visual Photoreception in Patients With Glaucoma: Impacts on Sleep, Alertness, Mood, and Cognition

ConditionGlaucoma
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-75
SponsorNational University of Singapore

About this trial

The goal of this study is to understand how light sensitivity in the eye affects sleep, mood, alertness, and cognition in adults with glaucoma compared to healthy individuals aged 45-75 years.

The main questions it aims to answer are:

1. Do patients with glaucoma experience poorer sleep, mood, alertness, and cognitive function than age-matched healthy adults? 2. Are these changes related to reduced light sensitivity in special retinal cells called intrinsically photosensitive retinal ganglion cells (ipRGCs), lost in glaucoma? 3. Can exposure to safe, full-spectrum indoor light help improve these functions?

Researchers will compare patients with glaucoma and age-matched healthy controls to see if differences in light sensitivity can explain changes in non-visual light responses (i.e., sleep, mood, alertness, and cognition) and whether full-spectrum light exposure can enhance alertness and wellbeing.

Participants will:

1. Complete eye exams and baseline questionnaires about their sleep, daytime sleepiness, mood, and wellbeing. 2. Wear a wrist-worn device for 8-16 days to record their sleep patterns and light exposure. 3. Visit the laboratory for cognitive and attention tests following exposure to two lighting conditions (randomized, cross-over):

* Standard indoor light (\~300 lux) * Full-spectrum light (\~1000 lux)

This study will help researchers understand how glaucoma affects the brain beyond vision and explore whether light-based interventions can improve quality of life for people living with glaucoma.

Eligibility criteria

Qualifiers

Patients with glaucoma must meet all of the inclusion criteria to participate in this study.

Patients diagnosed with primary open-angle glaucoma (POAG), as indicated by Humphrey Visual Field (HVF) mean deviation (VFMD) scores better than -12 dB in at least one eye during their most recent clinic visit.

Patients having spared central vision.

Patients aged 45 to 75 years old.

Disqualifiers

Participants with myopia exhibiting a refractive error exceeding -8.00 diopters (D)

Participants with a history of complicated previous intraocular surgery

Participants taking alpha-adrenergic agonist eye drops or other systemic medications or drugs that could affect the pupillary response

Participants with any past or current ocular condition (i.e., age-related retinal diseases (e.g., age-related macular degeneration), retinal pigment epithelium diseases (e.g., Best's disease), diabetic retinopathy, or other optic or generalized neuropathies, significant ocular trauma, or any eye condition affecting fixation (eg. Nystagmus)).

Trial design

Treatments tested in this trial

  • Full-spectrum light exposure
  • Standard indoor light exposure (Control)

Treatment groups

120 Participants
are divided into 2 treatment groups

Sponsors and collaborators

National University of Singapore

Lead sponsor

Singapore National Eye Centre

Collaborator

Singapore Eye Research Institute

Collaborator

National University Hospital, Singapore

Collaborator