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临床试验/CTRI/2025/10/096134
CTRI/2025/10/096134尚未招募2 期

Effectiveness of the Bates method v/s Oculomotor exercises on visual acuity and eye fatigue in individuals with Digital eye strain: A Randomized clinical trial

Harshawardhan kudale1 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2025年11月11日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
68
试验地点
1
主要终点
Patient satisfaction scale

研究概览

简要总结

This randomized clinical trial investigates the effectiveness of the Bates method compared to oculomotor rehabilitation in improving visual acuity and reducing eye fatigue in individuals experiencing digital eye strain (DES). DES is a common condition among frequent digital device users, characterized by symptoms such as eye discomfort, blurred vision, dryness, and headaches, resulting from prolonged screen exposure. The study targets computer users aged 18 to 40 years, with a particular focus on young adults aged 18-25.The research methodology involves assigning participants to either the Bates method group or the oculomotor rehabilitation group. The Bates method, a vision improvement technique developed by William H. Bates, aims to reduce eye muscle strain through relaxation exercises. Oculomotor rehabilitation focuses on enhancing eye muscle coordination, focus flexibility, and reducing symptoms of eye strain through targeted exercises. Visual acuity measurements are conducted using standardized tools such as the Snellen chart and dynamic visual acuity tests, while eye fatigue levels are evaluated using validated questionnaires like the Computer Vision Syndrome Questionnaire (CVS-Q).

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • Age group between 18-40years,People using Digital devices/viewing screen or with the screen time for 6 hours or more,CVS-Q score higher than or equal to 6 ,Willingness to participate.

排除标准

  • History of Systemic ocular pathology (diabetes mellitus, hypertension), History of Strabismic anomaly(hypertropia, hypotropia), People undergoing any kind of vision therapy, History of Hypermetropia, Myopia, Cataract, Glaucoma, History of Neurological disorders(Myasthenia gravis, Stroke, TBI, Optic neuritis).

结局指标

主要结局

Patient satisfaction scale

时间窗: which will be assessed at baseline and after 3 weeks

次要结局

  • Eye risk level questionnaire(which will be assessed at baseline & after 3 weeks)
  • Dynamic Visual Acuity(which will be assessed at baseline & after 3 weeks)

研究者

发起方
Harshawardhan kudale
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr sushmita badiger

KLES Institute of Physiotherapy Belgaum

研究点 (1)

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