Clinical Trials Directory

Trials / Completed

CompletedNCT04398212

Computer Vision Syndrome Visual Sequelae

Visual and Ocular Sequelae of Computer Vision Syndrome: A Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
733 (actual)
Sponsor
Sohag University · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

the university students will respond to CVS-F3 survey form and then they will be subjected to complete ophthalmic examination and investigations

Detailed description

CVS-F3 is a survey form consisted of up to 30 questions regarding Computer Vision Syndrome (CVS) complains, thereafter a randomized sample of students will be subjected to complete ophthalmic examination including visual acuity and refractive measurements, intraocular pressure measurements, Slitlamp and fungus examinations, mfERG examinations. the sudents will be requested to decrease their screen time and the examinations will be repeated one month later.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTmfERG (multifocal-retinogram)mfERG will be performed for the students to document the effect of CVS on retina

Timeline

Start date
2018-05-21
Primary completion
2020-06-15
Completion
2020-08-01
First posted
2020-05-21
Last updated
2020-08-10

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04398212. Inclusion in this directory is not an endorsement.

Computer Vision Syndrome Visual Sequelae (NCT04398212) · Clinical Trials Directory