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The Effects of Glasses-Free 3D Training on Visual and Cognitive Function in Presbyopic Individuals

NCT06853691 · tracked via the Priya Life Science China tracker
Phase
Not applicable
Started
2025-02-27
Last updated
2025-03-03

Condition(s) studied

Presbyopia

Investigational drug(s) / intervention(s)

glasses-free 3D visual training

glasses-free 3D visual training: Trail group Conduct 15 minutes of naked-eye 3D vision training. Twice a day, five days a week. Control groups The subjects watched ordinary 2D videos for 15 minutes each time, all under the same lighting conditions. This was done twice a day, five days a week.

Study summary

This study aims to evaluate the effectiveness of glasses-free 3D visual training in improving visual function, visual comfort, and the application ability of visual functions in individuals with presbyopia. The research will assess changes in brain activity related to visual processing using Electroencephalogram(EEG)and Functional near-infrared spectroscopy(NIRS) before and after the training. By examining the impact of stereoscopic stimulation on the functional connectivity of brain regions, the study seeks to provide new insights into the rehabilitation of presbyopia and its underlying mechanisms. The goal is to offer a non-invasive and scientifically supported approach to improving presbyopia treatment, potentially advancing clinical practices and contributing to brain science and ophthalmology

Eligibility

Sex
ALL
Min age
40 Years
Max age
60 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Age 40-60 years old, both sexes; 2. refractive error -6.0D to 5.0D, astigmatism \<2.0D, anisometropia \<4.0D; 3. binocular corrected visual acuity \<0.2LogMAR; 4. stereoscopic threshold ≤100 '; 5. The subjects could understand the purpose of this study and sign the informed consent. Exclusion Criteria: 1. after lens replacement; People with cataracts, which affect vision, have other eye conditions such that simultaneous vision is not possible; 2. using any medication known to affect accommodative function or wearing orthokeratology lenses in the past 1 month; 3. patients with severe systemic disease or severe mental illness; 4. Other situations where the investigator considers that the subject should not participate in the study for safety reasons or the interests of the patient.

Primary outcome measure(s)

  • Amplitude of accommodation — Baseline and after 6 and 12 weeks of training
    The push-up method combined with negative lens method was used. The measurements were completed by a comprehensive refractometer. It was performed according to the methods in Clinical Procedures for Ocular Examination 4th

Trial sites (1)

FacilityCityRegionStatus
Zhongshan Opthalmic Center, Sun Yat-sen University Guangzhou Guangdong
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06853691 on ClinicalTrials.gov ↗ ← All trials in China