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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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Development and validation of a web-based reading test for normal and low vision patients

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Autor
Labiris G., Panagiotopoulou E.-K., Duzha E., Tzinava M., Perente A., Konstantinidis A., Delibasis K.
Datum
2021
Language
en
DOI
10.2147/OPTH.S314943
Schlagwort
adult
Article
calculation
calibration
clinical article
clinical trial
computer vision
controlled study
correlation coefficient
Democritus Digital Acuity Reading Test
female
human
low vision
male
middle aged
presbyopia
prospective study
reading
reading test
test retest reliability
validation study
web-based intervention
Dove Medical Press Ltd
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Zusammenfassung
Purpose: To develop and validate a web-based reading test for normal and low vision patients. Methods: This is a prospective, comparative trial. The web-based Democritus Digital Acuity Reading Test (wDDART) was developed. wDDART introduces a series of advanced characteristics (advanced text calibration, computer-vision-based estimation of patient’s distance, and automatic calculation of patient’s reading times) that facilitate the overall examination procedure. wDDART’s reading parameters [reading acuity (RA), maximum reading speed (MRS), critical print size (CPS) and reading accessibility index (ACC)] were compared to the corresponding ones of its conventional Windows-based reading test (DDART) in a sample of normal and low vision participants. wDDART’s test–retest reliability for all reading parameters was evaluated in a 15-day time-window. Results: One hundred patients (normal vision group-NVG: 70; low vision group-LVG: 30 patients) responded to DDART and wDDART. Non-significant differences between the two reading tests were found for all parameters in NVG and LVG. Intraclass correlation coeffi-cients (ICCs) between the two tests demonstrated good or excellent correlation for RA, MRS, ACC and moderate correlation for CPS. Test–retest reliability was excellent for RA and ACC, while ICCs were 0.715–0.895 for MRS and CPS. Conclusion: The wDDART demonstrated sufficient validity and repeatability making it suitable for clinical and research settings. Clinicaltrials.gov Identifier: NCT04618224. © 2021 Labiris et al.
URI
http://hdl.handle.net/11615/75615
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