Clinical Trials Directory

Trials / Completed

CompletedNCT05187221

Prevalence and Sequelae of Computer Vision Syndrome in Egyptian Universities

Visual, Ocular Surface and Extraocular Diagnostic Criteria for Prevalence of Computer Vision Syndrome: A Cross-sectional Smart-survey Based Study

Status
Completed
Phase
Study type
Observational
Enrollment
8,085 (actual)
Sponsor
Sohag University · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Accepted

Summary

CVS-F4 questionnaire will be used as an instrument to survey CVS prevalence and severity among medical students

Detailed description

CVS-F4 (30 questions) will be an online survey via the SurveyMonkey Company. We will collect the responses and analyze the results. Informed consent will be obtained from the participants as an item within the survey itself that he/she agrees to use his/her data in this research work. The questionnaire includes questions regarding potential ocular, extra-ocular, musclo-skeletal and neuro-psychatric complains caused by CVS. Complete statistical analysis of the survey data will be done using univariate and multivariate logistic and linear regression analysis. The CVS diagnosis will be based on the 5 diagnostic criteria (5DC) to create a new short self-assessment questionnaire for accurate prevalence of CVS.

Conditions

Interventions

TypeNameDescription
BEHAVIORALCVS GroupCVS-F4 will be an online survey via the SurveyMonkey Company. The participants will report their potential CVS complains and associated screen factors as screen-time, screen-size, screen-resolution and other factors. We will collect the responses and analyse the results. Informed consent will be obtained from the participants as an item within the survey itself that he/she agrees to use his/her data in this research work. This group will contain participants with CVS complains.

Timeline

Start date
2021-12-30
Primary completion
2022-05-20
Completion
2022-09-01
First posted
2022-01-11
Last updated
2024-05-29

Locations

2 sites across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05187221. Inclusion in this directory is not an endorsement.