Analyzing eye health effects from prolonged screen use
Official title: Analysis of Visual and Ocular Outcomes of Computer Vision Syndrome
Run by Sohag University · NCT06106347 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study is testing how spending a lot of time on screens affects the eye health of university students and young staff members aged 20-30.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 20 Years to 30 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Sohag University Academic / other |
| Locations | 1 site (Sohag) |
| Trial ID | NCT06106347 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are university students and young staff members aged 20-30 who use screens for more than three hours daily.
✕Probably not a fit
Patients with significant eye conditions such as amblyopia, strabismus, or high refractive errors may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study investigates the visual and ocular outcomes associated with Computer Vision Syndrome (CVS) among university students and young staff members who spend significant time on digital screens. Participants aged 20-30, who have been using screens for more than three hours daily over the past three years, will be assessed using a multifocal electroretinography (mfERG) device to evaluate their eye health. The study aims to enhance understanding of the impact of digital technology on visual performance and overall eye health, addressing misconceptions and promoting protective measures through educational programs.
Why it matters
Potential benefit: If successful, this study could lead to improved awareness and strategies for mitigating the adverse effects of prolonged screen use on eye health.
How similar studies have gone: Other studies have explored the effects of screen time on eye health, indicating a growing body of evidence, but this specific approach using mfERG is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * include university students and young staff members, 20-30 years old who were spending more than 3 screen-hours daily on average over the last 3 years. Exclusion Criteria: * include amblyopia; strabismus; anisometropia; refractive errors higher than 4 D myopia, 4 D hyperopia, or 4 D astigmatism; difference between subjective and cycloplegic refraction \>1D; and previous or current systemic or eye disease or surgery.
Where it's running
-
Sohag University hospitals
Sohag, Egypt Recruiting
Study contacts
- Study coordinator: Mostafa R Refaee, Resident
- Email: refatsasa3@gmail.com
- Phone: 01125795711
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Protecting gamers' eyes with lubricating eyedrops
This study tests if TheaLoz Duo lubricating eyedrops can help gamers with dry eyes feel better after long hours of screen time.
-
Trauma registry at Sohag University Hospital
This study tests the creation of a trauma registry in the emergency department to collect data on injured adults admitted with polytrauma at Sohag University Hospital.
-
Prevalence of Myocardial Bridging and its relation to Coronary Plaques on MDCT
This study tests how common myocardial bridging is and whether it relates to coronary plaque in patients undergoing coronary CT angiography.
-
Septoplasty: see if it changes headache symptoms
This study tests whether septoplasty can change headache severity in adults with septal deviation and headache.
-
Predicting SLE Flares with Patient Reports and Machine Learning
Aims to test a low-cost, patient-reported outcome–based machine learning tool to see if it can detect lupus flares early and support care, especially in settings with limited resources.
-
Is geographic mismatch linked to short-term major heart problems after long drug-eluting stent placement?
This study checks whether geographic mismatch can predict short-term major adverse cardiovascular events after a long drug-eluting stent is placed in the coronary arteries.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.