Status:

RECRUITING

Optimal Non-invasive Brain Stimulation for Peripheral Vision

Lead Sponsor:

The Hong Kong Polytechnic University

Collaborating Sponsors:

Chinese University of Hong Kong

The University of Hong Kong

Conditions:

Glaucoma

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief Summary

Glaucoma is a complex disease that can result in progressive vision loss. There are no treatments that restore vision lost to glaucoma. However, recent studies have shown that vision can be improved b...

Detailed Description

This study uses a within-subjects, double-blind, placebo-controlled design and will be carried out in Hong Kong (The Hong Kong Polytechnic University). Participants who will be recruited are 40 glauc...

Eligibility Criteria

Inclusion

  • Age range from 18 to 80 years;
  • Diagnosis of primary open angle or normal tension glaucoma with relative scotoma in both eyes;
  • A relative scotoma defined as a Humphrey Field Analyser (HFA) threshold perimetry loss (mean deviation of ≤-6dB) within the central 30° of the visual field for at least one eye;
  • Best-corrected distance visual acuity of 6/12 or better (equivalent to 0.3 logMAR acuity or better to confirm that participant's central vision is preserved);
  • Stable vision and visual field loss for at least 3 months;
  • With a cognitive functional score of 22 or above in the Montreal Cognitive Assessment - Hong Kong version (HK-MoCA) (to confirm participant's intact cognitive function).

Exclusion

  • Ocular diseases other than glaucoma (e.g. age-related macular degeneration, diabetic retinopathy, moderate to severe cataract) or severe hearing impairment (to ensure that participant can hear the instructions clearly during assessments and training);
  • Severe medical problems (e.g. stroke, Parkinson's disease) or self-reported neurological (e.g. brain surgery, brain tumor, peripheral neuropathy), or cognitive disorders (e.g. diagnosed dementia or cognitive impairment);
  • Self-reported vestibular or cerebellar dysfunction, history of vertigo;
  • Using any medications for any neurological conditions or psychiatric drugs (e.g. sedative, hypnotic) that might interfere with motor control;
  • Contraindications for non-invasive brain stimulation.

Key Trial Info

Start Date :

November 1 2021

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

September 1 2025

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT04846140

Start Date

November 1 2021

End Date

September 1 2025

Last Update

October 29 2024

Active Locations (1)

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Allen MY Cheong

Hong Kong, China