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Turkish Version of Digital Eye Strain Questionnaire (DESQ)

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ClinicalTrials.gov Identifier: NCT06054542
Recruitment Status : Not yet recruiting
First Posted : September 26, 2023
Last Update Posted : September 26, 2023
Sponsor:
Information provided by (Responsible Party):
Ayse Unal, Alanya Alaaddin Keykubat University

Study Description
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Brief Summary:
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.

Condition or disease Intervention/treatment
Cultural Adaptation Reliability Validity Adults Eye Strain Other: Cultural adaptation, reliability and validity

Study Design
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Study Type : Observational
Estimated Enrollment : 130 participants
Observational Model: Other
Time Perspective: Prospective
Official Title: Validity and Reliability of the Turkish Version of Digital Eye Strain Questionnaire (DESQ)
Estimated Study Start Date : October 2023
Estimated Primary Completion Date : May 2024
Estimated Study Completion Date : June 2024
Groups and Cohorts
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Intervention Details:
  • Other: Cultural adaptation, reliability and validity
    Cross-cultural Adaptation, Reliability and Validity of the Turkish Version of the DESQ

Outcome Measures
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Primary Outcome Measures :
  1. DESQ [ Time Frame: 10 minutes ]
    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)


Eligibility Criteria
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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study 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
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
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT06054542


Contacts
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Contact: Ayşe Ünal, Assoc. Prof. +90(242)510 6060 ext 4329 pt.aunal@gmail.com
Contact: Ayça Aracı, Asst. Prof. +90(242)510 6060 ext 4338 ayca.araci@alanya.edu.tr

Sponsors and Collaborators
Alanya Alaaddin Keykubat University
More Information
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Responsible Party: Ayse Unal, Assoc. Prof., Alanya Alaaddin Keykubat University
ClinicalTrials.gov Identifier: NCT06054542    
Other Study ID Numbers: 20.09.2023/DESQ
First Posted: September 26, 2023    Key Record Dates
Last Update Posted: September 26, 2023
Last Verified: September 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Asthenopia
Sprains and Strains
Wounds and Injuries
Eye Diseases