A Pain Reporting Platform for Adolescents with Sickle-Cell Disease

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dc.contributor.authorGary, Kevin
dc.contributor.authorRallabhandi, Pooja
dc.contributor.authorQuezado, Zenaide
dc.contributor.authorCleary, Kevin
dc.date.accessioned2019-01-03T00:20:56Z
dc.date.available2019-01-03T00:20:56Z
dc.date.issued2019-01-08
dc.description.abstractThis paper presents the latest version of the Pain Reporting and Management mHealth Platform for adolescent Sickle Cell Disease, developed in collaboration by Arizona State University and the Children’s National Health System. This platform supports a cross-platform mHealth app, reporting and task management API, and portal dashboard for care provider monitoring. Extending our prior work, the latest version adds enhanced app features (games, power-ups, badges, notifications) to promote sustained adherence to the reporting protocol, and enhanced reporting features for providers that track high fidelity compliance measures and aggregate outcome scores. This paper summarizes the architecture and principle features of the platform, and presents data supporting improved compliance.
dc.format.extent8 pages
dc.identifier.doi10.24251/HICSS.2019.472
dc.identifier.isbn978-0-9981331-2-6
dc.identifier.urihttp://hdl.handle.net/10125/59826
dc.language.isoeng
dc.relation.ispartofProceedings of the 52nd Hawaii International Conference on System Sciences
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectICT-enabled Self-management of Chronic Diseases and Conditions
dc.subjectInformation Technology in Healthcare
dc.subjectchronic disease, mHealth, software architecture, usability
dc.titleA Pain Reporting Platform for Adolescents with Sickle-Cell Disease
dc.typeConference Paper
dc.type.dcmiText

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