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Recruiting NCT06054542

Turkish Version of Digital Eye Strain Questionnaire (DESQ)

— Observational Cultural Adaptation Reliability Validity Adults

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Cultural adaptation, reliability and validity.
Who it may be relevant to
Registry conditions: Cultural Adaptation, Reliability, Validity, Adults. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Validity and Reliability of the Turkish Version of Digital Eye Strain Questionnaire (DESQ)

Overview

The aims of this study were to perform cultural adaptation of the DESQ and provide information regarding the factor structure, reliability and validity of the instrument in Turkish speaking adults.

Interventions

  • Other Cultural adaptation, reliability and validity
    Cross-cultural Adaptation, Reliability and Validity of the Turkish Version of the DESQ

Primary outcome measures

  • DESQ [Time frame: Baseline and after 7 days]

Eligibility criteria

Inclusion criteria

  • Between the ages of 18-65 years
  • People who spend two or more continuous hours a day on their digital devices (computer, tablet, smartphone) or use more than one device

Exclusion criteria

  • History of ophthalmic surgery or active ocular disease
  • Participants who did not understand the instructions or did not sign a consent form were excluded

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

Turkey (Türkiye) · 1 center
  • Alanya Alaadin Keykubat University — Antalya

Identifiers

NCT: NCT06054542 · 20.09.2023/DESQ

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗