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Design, Implementation, and Usability Evaluation of the Iranian Primary Vitiligo Patient Registry Publisher



Arabkermani Z1, 2 ; Sharifian R1 ; Aryanian Z3, 4 ; Bastani P1 ; Esmaeli N3 ; Bashiri A1 ; Sheikhtaheri A5
Authors
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Authors Affiliations
  1. 1. Department of Health Information Management, School of Health Management and Information Sciences, Health Human Resources Research Center, Clinical Education Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
  2. 2. Razi Hospital Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Autoimmune Bullous Diseases Research Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Dermatology, Babol University of Medical Sciences, Babol, Iran
  5. 5. Department of Health Information Management, School of Health Management and Information Sciences, Iran University of Medical Sciences, Tehran, Iran

Source: Journal of the Dermatology Nurses' Association Published:2023


Abstract

Introduction Vitiligo is an acquired pigmentary disorder, which is usually progressive and irreversible if left untreated. Structured databases such as registries are required to continuously collect standard data about patients with the same disease. Objectives This study aimed to design and implement a vitiligo registry and evaluate its usability in Iran. Methodology This research was conducted in four stages: determining the minimum data set required for the registry, creating a conceptual model using unified modeling language diagrams and Sparx Enterprise Architect software, implementing the registry in the PhpStorm programming environment, and evaluating the software usability based on the responses of 17 end users to a questionnaire. Results The required data items, consisting of 127 items in eight categories, were approved by the experts and used to design the vitiligo registry. Then, the software was designed and implemented. In the assessment stage, the software received a 89.5% approval rate from its users. Conclusion Developing a vitiligo registry with high usability as well as making decisions based on the registry data can improve understanding of the disease and facilitate research in this field. As a result, high-quality services could be provided to patients nationwide. © Lippincott Williams & Wilkins.