Cultural adaptation of a questionnaire for digital eye strain in Turkish adults
Validity and Reliability of the Turkish Version of Digital Eye Strain Questionnaire (DESQ)
This study is testing a new version of a questionnaire about digital eye strain to see if it works well for Turkish adults who use screens for a few hours each day.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 130 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Alanya Alaaddin Keykubat University Academic / other |
| Locations | 1 site (Antalya) |
| Trial ID | NCT06054542 on ClinicalTrials.gov |
What this trial studies
This study aims to culturally adapt the Digital Eye Strain Questionnaire (DESQ) for Turkish-speaking adults and assess its reliability and validity. Participants aged 18 to 65 who use digital devices for two or more hours daily will be included. The study will evaluate the factor structure of the adapted questionnaire to ensure it accurately reflects the experiences of Turkish users. By focusing on cultural nuances, the research seeks to provide a reliable tool for assessing digital eye strain in this population.
Who should consider this trial
Good fit: Ideal candidates for this study are Turkish-speaking adults aged 18-65 who regularly use digital devices.
Not a fit: Patients with a history of ophthalmic surgery or active ocular disease may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a validated tool for better understanding and managing digital eye strain among Turkish-speaking adults.
How similar studies have performed: While cultural adaptation studies are common, the specific adaptation of the DESQ for Turkish speakers is a novel approach.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Antalya
- Alanya Alaadin Keykubat University — Antalya, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Ayşe Ünal, Assoc. Prof.
- Email: pt.aunal@gmail.com
- Phone: 0090(242)510 6060
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.