- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06054542
Turkish Version of Digital Eye Strain Questionnaire (DESQ)
September 20, 2023 updated by: Ayse Unal, Alanya Alaaddin Keykubat University
Validity and Reliability of the Turkish Version of Digital Eye Strain Questionnaire (DESQ)
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.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
130
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ayşe Ünal, Assoc. Prof.
- Phone Number: 4329 +90(242)510 6060
- Email: pt.aunal@gmail.com
Study Contact Backup
- Name: Ayça Aracı, Asst. Prof.
- Phone Number: 4338 +90(242)510 6060
- Email: ayca.araci@alanya.edu.tr
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
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
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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)
|
10 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
October 1, 2023
Primary Completion (Estimated)
May 1, 2024
Study Completion (Estimated)
June 1, 2024
Study Registration Dates
First Submitted
September 20, 2023
First Submitted That Met QC Criteria
September 20, 2023
First Posted (Actual)
September 26, 2023
Study Record Updates
Last Update Posted (Actual)
September 26, 2023
Last Update Submitted That Met QC Criteria
September 20, 2023
Last Verified
September 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20.09.2023/DESQ
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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