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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05209581
Other study ID # DUTh REC/4/16-12-2021
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 24, 2022
Est. completion date May 31, 2022

Study information

Verified date June 2023
Source Democritus University of Thrace
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The present research process is a prospective clinical study that will be conducted under the auspices of the Democritus University of Thrace (DUTH) in the open accommodation structure for refugees and immigrants of Kavala, Kavala, Greece, and the Pre-Removal Detention Center (PROKEKA) for Foreigners of Kos, Kos, Greece. The study aims to assess the basic ophthalmological condition of the refugee/immigrant population and is developed in two main areas: 1. The recording of the ophthalmological care that the refugee/immigrant has received until his/her inclusion in the study through a structured questionnaire (eg previous examinations, spectacle utilization, pharmaceutical or other interventions, etc.) 2. The measurement of monocular best-spectacle corrected visual acuity in both eyes using a web-based visual acuity chart. Adult participants living in the two aforementioned centers will be recruited in a consecutive-if-eligible basis. All age groups will be proportionally represented (proportional age distribution).


Description:

Study protocol will adheres to the tenets of the Helsinki Declaration and written informed consent translated in the language of each examinee will be obtained by all participants. Subsequently, participants will complete a questionnaire about demographic and general clinical information. Then, the best spectacle-corrected distance visual acuity of each participant's both eyes will be evaluated monocularly via a web-based digital chart in a high-resolution screen. The same environmental lighting conditions and the same screen brightness will be applied. The examination will be performed at the same predetermined viewing distance. Finally, according to each participant's visual acuity, appropriate instructions will be given for the improvement of his/her eye care.


Recruitment information / eligibility

Status Completed
Enrollment 330
Est. completion date May 31, 2022
Est. primary completion date April 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Adult refugees or immigrants Exclusion Criteria: - Visual acuity lower than 1.0 LogMAR - Age <18 years - Refugees or immigrants living in the accommodation structures without yet having the appropriate legal documents

Study Design


Intervention

Diagnostic Test:
Distance Visual Acuity Examination
Best spectacle-corrected distance visual acuity of refugees/immigrants will be examined via a web-based digital visual acuity chart

Locations

Country Name City State
Greece Democritus University of Thrace Alexandroupolis Evros

Sponsors (1)

Lead Sponsor Collaborator
Democritus University of Thrace

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Primary Best spectacle-corrected distance visual acuity Best spectacle-corrected distance visual acuity of refugees will be examined via a web-based digital visual acuity chart 1 week
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