Glaucoma Rehabilitation using ElectricAI Transcranial Stimulation (GREAT) – Study Protocol for Randomized Controlled Trial using Combined Perceptual Learning and Transcranial Electrical Stimulation for Vision Enhancement

Author:

Jia Shuwen1ORCID,Mei Xiaolin1,Chen Lilin1,Chan Lok Hin1,Tsang Celia1,Suen Venus1,Li Tingni1,Zaw Myo Win2,Liu Amanda2,Thompson Ben3,Sabel Bernhard4,Woo George1,Leung Christopher K.S.5,Yip Shea-ping6,Chang Dorita H. F.7,Cheong Allen M.Y.1ORCID

Affiliation:

1. The Hong Kong Polytechnic University School of Optometry

2. Centre for Eye and Vision Research Limited, Hong Kong Science Park

3. University of Waterloo, School of Optometry and Vision Science

4. University of Magdeburg, Institute of Medical Psychology

5. TThe University of Hong Kong, Department of Opthalmology

6. The Hong Kong Polytechnic University Department of Health Technology and Informatics

7. The University of Hong Kong Department of Psychology

Abstract

Abstract

Background: Glaucoma patients with irreversible visual field loss often experience decreased quality of life, impaired mobility, and mental health challenges. Perceptual learning (PL) and transcranial electrical stimulation (tES) have emerged as promising interventions for vision rehabilitation, showing potential in restoring residual visual functions. The Glaucoma Rehabilitation using ElectricAI Transcranial stimulation (GREAT) project aims to investigate whether combining PL and tES is more effective than using either method alone in maximizing the visual function of glaucoma patients. Additionally, the study will assess the impact of these interventions on brain neural activity, blood biomarkers, mobility, mental health, quality of life, and fear of falling. Methods: The study employs a three-arm, double-blind, randomized, superiority-controlled design. Participants are randomly allocated in a 1:1:1 ratio to one of three groups receiving: (1) real PL and real tES (2) real PL and sham tES, and (3) placebo PL and sham tES. Each participant undergoes 10 sessions per block (~ 1 hour each), with a total of three blocks. Assessments are conducted at six time points: baseline, interim 1, interim 2, post-intervention, 1-month post-intervention, and 2-month post-intervention. The primary outcome is the mean deviation of the 24 − 2 visual field measured by the Humphrey Visual Field Analyzer. Secondary outcomes include detection rate in the suprathreshold visual field, balance and gait functions, and electrophysiological and biological responses. This study also investigates changes in neurotransmitter metabolism, biomarkers, self-perceived quality of life, and psychological status before and after the intervention. Discussion: The GREAT project is the first study to assess the effectiveness of PL and tES in the rehabilitation of glaucoma. Our findings will offer comprehensive assessments of the impact of these treatments on a wide range of brain and vision-related metrics including visual field, neural activity, biomarkers, mobility, mental health, fear of falling and quality of life. Trial registration: ClinicalTrials.gov NCT05874258. Registered on 15th May 2023 URL: https://clinicaltrials.gov/study/NCT05874258?cond=NCT05874258&rank=1

Publisher

Springer Science and Business Media LLC

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