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

NCT ID: NCT05675475

Last Updated: 2023-01-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

400 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-01-31

Study Completion Date

2023-06-30

Brief Summary

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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.

Detailed Description

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Conditions

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Digital Eye Strain

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Interventions

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Exposure

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

Intervention Type OTHER

Orthoptic assessment (Outcome measure)

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.

Intervention Type DIAGNOSTIC_TEST

Tear 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.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

39 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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NOVA Medical School | Faculdade de Ciências Médicas, Universidade Nova de Lisboa

UNKNOWN

Sponsor Role collaborator

Escola Superior de Tecnologia da Saúde de Lisboa (ESTeSL)

UNKNOWN

Sponsor Role collaborator

University of Évora

OTHER

Sponsor Role collaborator

CINTESIS@RISE, NOVA Medical School | Faculdade de Ciências Médicas, Universidade Nova de Lisboa

UNKNOWN

Sponsor Role collaborator

Comprehensive Health Research Center (CHRC), Universidade Nova de Lisboa

UNKNOWN

Sponsor Role collaborator

Universidade Nova de Lisboa

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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André Rosário, PhD

Role: PRINCIPAL_INVESTIGATOR

NOVA Medical School | Faculdade de Ciências Médicas, Universidade Nova de Lisboa

Carla Lança, PhD

Role: PRINCIPAL_INVESTIGATOR

Escola Superior de Tecnologia da Saúde de Lisboa (ESTeSL)

Locations

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Escola Superior de Tecnologia de Saúde de Lisboa

Lisbon, , Portugal

Site Status

Countries

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Portugal

Central Contacts

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Carla Lança, PhD

Role: CONTACT

+351218980421

Maria Barata, MSc

Role: CONTACT

Facility Contacts

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Carla Lança, PhD

Role: primary

+351218980421

Maria Barata, MSc

Role: backup

Other Identifiers

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DESIROUS

Identifier Type: -

Identifier Source: org_study_id

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