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Usability of the Software MacuFix for the Categorization of Metamorphopsia — MacuFix  

Vision Disorders Clinical Trial

Official title:
Usability of the Software MacuFix for the Categorization of Metamorphopsia and Evaluation of Patient Adherence Compared to the Amsler Grid

Clinical Trial Summary

The usability of a novel test to categorize a distorted visual impression (metamorphopsia) is examined with the questionnaire "SUS"

Clinical Trial Description

Introduction Diseases of the retinal centre (macula) can lead to a distorted visual impression (metamorphopsia). The usability of a novel on-screen test to categorize metamorphopsia is to be examined with the questionnaire "SUS" to determine how user-friendly the software is perceived. Purpose To examine the usability of the software for persons perceiving metamorphopsia employing the questionnaire SUS. Aim of the work Improvement of the software in terms of user-friendliness. Methods For this observational pilot study, 30 persons are to be recruited from the patient pool of a private practice. Primary endpoint: Score of the SUS questionnaire. Each participating person performs the test once with each eye wearing appropriate near correction. The test shows on a screen 4 square fields with a grid pattern of horizontal and vertical lines. All 4 fields have lines that are partially distorted. The task of the test person is to select the field with more distinctively distorted lines when viewed with one eye.This selection must be made at least 10 times per eye: an algorithm determines the smallest correctly named distortion difference. Afterwards each person answers the System Usability Scale (SUS) questionnaire, SUS contains five positive and five negative statements on the usability of the system being evaluated. For each statement, the study participant gives his or her approval or rejection in the form of a scale ranging from 1= "strong approval" to 5= "strong rejection" of the statement. The results of the SUS questionnaire are used to calculate a numerical value (SUS score). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04347564
Study type Observational
Source Augenheilkunde Lindenthal
Contact
Status Completed
Phase
Start date May 4, 2020
Completion date September 30, 2020
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