Turkish Version of Digital Eye Strain Questionnaire (DESQ)
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorAlanya Alaaddin Keykubat University
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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
Disqualifiers
History of ophthalmic surgery or active ocular disease
Participants who did not understand the instructions or did not sign a consent form were excluded
Trial population
Healthy adults who spend two or more continuous hours a day on their digital devices (computer, tablet, smartphone) or use more than one device
Trial design
Design model
Other
Time perspective
Prospective
Treatments tested in this trial
Cultural adaptation, reliability and validity
Other interventionCross-cultural Adaptation, Reliability and Validity of the Turkish Version of the DESQ
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
DESQ
Digital Eye Strain Questionnaire (DESQ) is a thirteen-item self-report scale in a yes-no format designed to offer a measure of complaints related to digital eye strain syndrome (DES)
Time frame
Baseline and after 7 daysSponsors and contacts
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Source ClinicalTrials.gov