A single blind, randomized, comparative clinical trial evaluating the effectiveness of homoeopathic remedies Belladona 6C versus Euphrasia 6C in the management of screen induced Asthenopia
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- 1. Improved if the CVS-Q score is less than 6 after the treatment
研究概览
简要总结
Asthenopia commonly referred to as digital eye strain or computer vision syndrome is an increasingly prevalent condition associated with prolonged use of digital devices It manifests as visual discomfort headaches blurred vision dry eyes and reduced visual efficiency significantly affecting quality of life and occupational productivity Conventional management primarily involves ergonomic measures and optical corrections which provide only temporary relief Homoeopathy with its individualized and holistic approach offers potential as a safe and effective complementary treatment This single blind randomized comparative clinical trial is designed to evaluate the effectiveness of two homoeopathic remedies Belladonna 6C versus Euphrasia 6C in the management of screen induced asthenopia A total of 30 participants aged 18 to 40 years meeting inclusion criteria with Computer Vision Syndrome Questionnaire CVS Q scores more than or equal to 6 will be randomized into two groups Group A receiving Belladonna 6C and Group B receiving Euphrasia 6C each administered once weekly for three months along with daily placebo All participants will also receive standardized ergonomic advice for digital device usage Outcome assessment will be based on changes in CVS Q scores recorded at baseline and during follow ups every 15 days The primary objective is to compare the reduction in subjective symptoms between the two groups Secondary objectives include evaluating improvements in visual comfort performance during screen related tasks and the duration of sustained improvement The study seeks to provide clinical evidence regarding the comparative effectiveness of Belladonna 6C and Euphrasia 6C in screen induced asthenopia aiming to contribute to the development of a specific therapeutic protocol in homoeopathic practice for managing digital eye strain
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant 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
- •1 Adults aged 18-40 years of both sexes 2 Participants having eye symptoms because of prolong digital device use having CVS-Q score more than or equal to 6 will only be included irrespective of the use of spectacles 3 Regular digital device users for minimum 5 hours daily for at least 5 days per week.
排除标准
- •1 Pre-existing ocular pathology 2 Use of contact lenses 3 History of ocular surgery within the past year 4 Current treatment with lubricating eye drops or other interventions for DES that cannot be discontinued 5 Systemic conditions that may affect tear production 6 Use of medications known to cause dry eyes 7 Pregnancy or breastfeeding 8 Chronic migraine or chronic headache 9 Below 18 and above 40 years of age.
结局指标
主要结局
1. Improved if the CVS-Q score is less than 6 after the treatment
时间窗: CVS-Q score assessed at baseline, 3 months and 6 months
2. Not improved if CVS-Q score is same or more than the pre-treatment score
时间窗: CVS-Q score assessed at baseline, 3 months and 6 months
次要结局
- Determine the duration of sustained improvement(6 months)
研究者
Dr Aditi Mahendra Deshmukh
Bharati Vidyapeeth (Deemed To Be University) Homoeopathic Medical College and Homoeopathic Hospital
