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Study of the Association Between Digital Eye Syndrome With Binocular Vision and the Ocular Surface in Higher Education Students in the Area of Health Technologies

Study of the Association Between Digital Eye Syndrome With Binocular Vision and the Ocular Surface in Higher Education Students in the Area of Health Technologies

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05675475
Acronym
DESIROUS
Enrollment
400
Registered
2023-01-09
Start date
2023-01-31
Completion date
2023-06-30
Last updated
2023-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Digital Eye Strain

Keywords

accommodation, convergence, tear film

Brief summary

The goal of this observational study is to determinate the association between DES and changes in binocular vision and ocular surface. in higher education students in the area of health technologies. The main questions it aims to determine the prevalence of Digital Eye Syndrome (DES); the association between DES and changes in binocular vision and ocular surface; whether the time of use and the type of electronic devices influences the degree and type of symptoms of DES; and to determine whether there is an association between the type of ametropia and the symptoms of DES. Participants will have to answer 3 questionnaires (the Computer Vision Syndrome Questionnaire; the Convergence Insufficiency Symptoms Survey, and the Dry Eye Questionnaire (DEQ-5)) and then they will perform an orthoptic assessment and an assessment of the ocular surface with the tear film Break Up Time (BUT) test.

Interventions

OTHERExposure

Higher education students from health technologies field exposed to digital devices.

The orthoptic assessment is a non-invasive assessment that will last for 30 min to determine visual parameters related to binocular vision. It will be carried out by the research team in the orthoptics and vision sciences laboratories of the Lisbon School of Health Tecnology.

DIAGNOSTIC_TESTTear film Break Up Time (BUT) test (Outcome measure)

The BUT test is a tear film rupture assessment test that allows the stability of the tear film to be evaluated. To perform these tests, it is necessary to instill fluorescein and then it is observed in the slit lamp under illumination with a cobalt blue filter, to count the break-up time.

Sponsors

NOVA Medical School | Faculdade de Ciências Médicas, Universidade Nova de Lisboa
CollaboratorUNKNOWN
Escola Superior de Tecnologia da Saúde de Lisboa (ESTeSL)
CollaboratorUNKNOWN
University of Évora
CollaboratorOTHER
CINTESIS@RISE, NOVA Medical School | Faculdade de Ciências Médicas, Universidade Nova de Lisboa
CollaboratorUNKNOWN
Comprehensive Health Research Center (CHRC), Universidade Nova de Lisboa
CollaboratorUNKNOWN
Universidade Nova de Lisboa
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 39 Years
Healthy volunteers
Yes

Inclusion criteria

* Students of the first, second and third year of the degrees offered by Lisbon School of Health Technology, Instituto Politécnico de Lisboa; * Age between 18 to 39 years; * Accept and sign the consent.

Exclusion criteria

* Working Students; * Students with known binocular vision disorders; * Previous eye surgeries.

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of Digital Eye SyndromeImmediately after subject enrollment, up to 1 week (single point collection)To verify the existence or absence of digital fatigue syndrome in higher education students. For this purpose, the Computer Vision Syndrome Questionnaire will be used. To verify the existence or not of digital fatigue syndrome in higher education. The Computer Vision Syndrome Questionnaire (CVS-Q) will be applied, which is composed of 16 x 2 questions, to assess the symptoms and their intensity. This questionnaire makes it possible to classifying CVS as asymptomatic and symptomatic.

Secondary

MeasureTime frameDescription
Dry Eye Questionnaire (DEQ-5)Immediately after subject enrollment, up to 1 week (single point collection)The DEQ-5 questionnaire is the reduced version of the DEQ questionnaire that allows the assessment of dry eye. this questionnaire is made up of 5 questions and allows to obtain an answer score that classifies as normal and dry eye.
Far Visual AcuityImmediately after subject enrollment, up to 1 week (single point collection)Visual acuity is the spatial resolution capability of the visual system. The unit of measurement for this variable will be the minimum resolution angle algorithm (LogMAR).
Near Visual AcuityImmediately after subject enrollment, up to 1 week (single point collection)Visual acuity is the spatial resolution capability of the visual system. The unit of measurement for this variable will be the minimum resolution angle algorithm (LogMAR).
Far Cover TestImmediately after subject enrollment, up to 1 week (single point collection)The cover test is one of the variables used to study the motor component of the visual system and is a categorical variable, which will allow the identification of latent and manifest ocular deviations.
Near Cover TestImmediately after subject enrollment, up to 1 week (single point collection)The cover test is one of the variables used to study the motor component of the visual system and is a categorical variable, which will allow the identification of latent and manifest ocular deviations.
Near StereopsisImmediately after subject enrollment, up to 1 week (single point collection)Stereopsis is one of the binocular vision parameters and the measurement unit used will be the arc seconds.
Near Point of ConvergenceImmediately after subject enrollment, up to 1 week (single point collection)The near point of convergence is one of the convergence assessment methods and the unit of measurement is cm.
Convergence Insufficiency Symptoms SurveyImmediately after subject enrollment, up to 1 week (single point collection)The main objective of this questionnaire is to assess the frequency of symptoms of visual discomfort and consists of fifteen questions. The answers to the questions are evaluated and allow classifying binocular vision into norm, suspected convergence insufficiency and convergence insufficiency.
Amplitude of AccommodationImmediately after subject enrollment, up to 1 week (single point collection)The amplitude of accomodation is one of the accommodation evaluation parameters and its measurement unit is diopters.
Far ConvergenceImmediately after subject enrollment, up to 1 week (single point collection)The far convergence is one of the elements of fusional vergencies and its measurement unit is the prismatic diopters.
Near ConvergenceImmediately after subject enrollment, up to 1 week (single point collection)The near convergence is one of the elements of fusional vergencies and its measurement unit is the prismatic diopters.
Near DivergenceImmediately after subject enrollment, up to 1 week (single point collection)The near divergence is one of the elements of fusional vergencies and its measurement unit is the prismatic diopters.
Far DivergenceImmediately after subject enrollment, up to 1 week (single point collection)The far divergence is one of the elements of fusional vergencies and its measurement unit is the prismatic diopters.
Break Up Time TestImmediately after subject enrollment, up to 1 week (single point collection)The BUT Test will allow assessing the stability of the tear film and the unit of measurement will be seconds.
Refrative ErrorImmediately after subject enrollment, up to 1 week (single point collection)The refractive error will be assessed using the auto refratometer and your measurements will be in diopters.
Flexibility of AccommodationImmediately after subject enrollment, up to 1 week (single point collection)The flexibility of accommodation is one of the accommodation evaluation parameters and its measurement unit is cycle per minute.

Countries

Portugal

Contacts

Primary ContactCarla Lança, PhD
carla.costa@estesl.ipl.pt+351218980421
Backup ContactMaria Barata, MSc
d52905@alunos.uevora.pt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026