Conceptualization and implementation of the central information portal on rare diseases: Protocol for a qualitative study

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dc.identifier.uri http://dx.doi.org/10.15488/3771
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/3805
dc.contributor.author Litzkendorf, Svenja
dc.contributor.author Hartz, Tobias
dc.contributor.author Göbel, Jens
dc.contributor.author Storf, Holger
dc.contributor.author Pauer, Frédéric
dc.contributor.author Babac, Ana
dc.contributor.author Lührs, Verena
dc.contributor.author Bruckner-Tuderman, Leena
dc.contributor.author Schauer, Franziska
dc.contributor.author Schmidtke, Jörg
dc.contributor.author Biehl, Lisa
dc.contributor.author Wagner, Thomas O.F.
dc.contributor.author Schulenburg, Johann-Matthias Graf von der
dc.contributor.author Frank, Martin
dc.date.accessioned 2018-10-08T12:30:55Z
dc.date.available 2018-10-08T12:30:55Z
dc.date.issued 2018
dc.identifier.citation Litzkendorf, S.; Hartz, T.; Göbel, J.; Storf, H.; Pauer, F. et al.: Conceptualization and implementation of the central information portal on rare diseases: Protocol for a qualitative study. In: Journal of Medical Internet Research 20 (2018), Nr. 5, e112. DOI: https://doi.org/10.2196/resprot.7425
dc.description.abstract Background: Recently, public and political interest has focused on people living with rare diseases and their health concerns. Due to the large number of different types of rare diseases and the sizable number of patients, taking action to improve the life of those affected is gaining importance. In 2013, the federal government of Germany adopted a national action plan for rare diseases, including the call to establish a central information portal on rare diseases (Zentrales Informationsportal über seltene Erkrankungen, ZIPSE). Objective: The objective of this study, therefore, was to conduct scientific research on how such a portal must be designed to meet the needs of patients, their families, and medical professionals, and to provide high-quality information for information seekers. Methods: We chose a 3-step procedure to develop a needs-based prototype of a central information portal. In the first step, we determined the information needs of patients with rare diseases, their relatives, and health care professionals by means of qualitative interviews and their content-analytical evaluation. On the basis of this, we developed the basic structure of the portal. In the second step, we identified quality criteria for websites on rare diseases to ensure that the information linked with ZIPSE meets the quality demands. Therefore, we gathered existing criteria catalogs and discussed them in an expert workshop. In the third step, we implemented and tested the developed prototypical information portal. Results: A portal page was configured and made accessible on the Web. The structure of ZIPSE was based on the findings from 108 qualitative interviews with patients, their relatives, and health care professionals, through which numerous information needs were identified. We placed particularly important areas of information, such as symptoms, therapy, research, and advisory services, on the start page. Moreover, we defined 13 quality criteria, referring to factors such as author information, creation date, and privacy, enabling links with high-quality information. Moreover, 19 users tested all the developed routines based on usability and comprehensibility. Subsequently, we improved the visual presentation of search results and other important search functions. Conclusions: The implemented information portal, ZIPSE, provides high-quality information on rare diseases from a central point of access. By integrating the targeted groups as well as different experts on medical information during the construction, the website can assure an improved search for information for users. ZIPSE can also serve as a model for other Web-based information systems in the field of rare diseases. eng
dc.language.iso eng
dc.publisher Toronto : JMIR Publications
dc.relation.ispartofseries Journal of Medical Internet Research 20 (2018), Nr. 5
dc.rights CC BY 4.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.subject Health information exchange eng
dc.subject Qualitative research eng
dc.subject Quality control eng
dc.subject Rare diseases eng
dc.subject.ddc 610 | Medizin, Gesundheit ger
dc.title Conceptualization and implementation of the central information portal on rare diseases: Protocol for a qualitative study eng
dc.type article
dc.type Text
dc.relation.issn 14388871
dc.relation.doi https://doi.org/10.2196/resprot.7425
dc.bibliographicCitation.issue 5
dc.bibliographicCitation.volume 20
dc.bibliographicCitation.firstPage e112
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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