Computer Vision Syndrome Visual Sequelae

Sohag University

Status: Completed

Conditions: Computer Vision Syndrome

Treatments: Diagnostic Test: mfERG (multifocal-retinogram)

Study type: Interventional

Funder types: Other

Identifiers

NCT04398212

5-10/4/2018

Details and patient eligibility

About

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

Full 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.

Enrollment: 733 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• University students

Exclusion criteria

• Amblyopia
• Anisometropia
• strabismus
• Previous eye surgery

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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733 participants in 2 patient groups, including a placebo group

Non-complaining group

Placebo Comparator group

Description:

the students in this group are not complaining of CVS symptoms but will be examined to diagnose CVS or exclude it

Treatment:

Diagnostic Test: mfERG (multifocal-retinogram)

Complaining group

Experimental group

Description:

the students in this group are complaining of CVS symptoms but will be examined to document their complains and correlate to clinical findings

Treatment:

Diagnostic Test: mfERG (multifocal-retinogram)