I’m Trying to Find my Way of Staying Organized: the Socio-Technical Assemblages of Personal Health Information Management

dc.contributor.authorWillis, Matthew
dc.date.accessioned2020-06-06T13:06:09Z
dc.date.available2020-06-06T13:06:09Z
dc.date.issued2019
dc.date.issued2019
dc.description.abstractPersonal health information management (PHIM) is a broad endeavor that requires the patient to navigate many different types of information. Including patients performing a variety of tasks and roles to make information useful. I ask the question: what practices constitute a patient’s personal health information management socio-technical assemblage? By doing this I am interested in understanding how PHIM is an assemblage of different actors, tools, technologies, information, and materialities that form a heterogeneous network to motivate the patient’s health maintenance and wellbeing. I describe information practices, planning and sense making practices that patients engage to begin to define this assemblage, and the social actors and materialities that manifest and stabilize. Then, I discuss three key commitments learned from this approach, namely: the personal aspect of PHIM, the role of physical and digital materials on PHIM, and the role of information practice materialities.de
dc.identifier.doi10.1007/s10606-019-09346-z
dc.identifier.pissn1573-7551
dc.identifier.urihttp://dx.doi.org/10.1007/s10606-019-09346-z
dc.identifier.urihttps://dl.eusset.eu/handle/20.500.12015/3755
dc.publisherSpringer
dc.relation.ispartofComputer Supported Cooperative Work (CSCW): Vol. 28, No. 6
dc.relation.ispartofseriesComputer Supported Cooperative Work (CSCW)
dc.subjectMaterialities
dc.subjectMy HealtheVet
dc.subjectPatient centered-care
dc.subjectPersonal health information management
dc.subjectPersonal health record
dc.subjectQualitative research
dc.subjectSocio-technical assemblage
dc.titleI’m Trying to Find my Way of Staying Organized: the Socio-Technical Assemblages of Personal Health Information Managementde
dc.typeText/Journal Article
gi.citation.endPage1102
gi.citation.startPage1073
gi.citations.count3
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gi.citations.elementSamantha A. Whitman, Kathleen H. Pine, Bjorg Thorsteinsdottir, Paige Organick-Lee, Anjali Thota, Nataly R. Espinoza Suarez, Erik W. Johnston, Kasey R. Boehmer (2021): Bodily Experiences of Illness and Treatment as Information Work: The Case of Chronic Kidney Disease, In: Proceedings of the ACM on Human-Computer Interaction CSCW2(5), doi:10.1145/3479527
gi.citations.elementAndri Färber, Christiane Schwabe, Philipp H Stalder, Mateusz Dolata, Gerhard Schwabe (2024): Physicians’ and Patients’ Expectations From Digital Agents for Consultations: Interview Study Among Physicians and Patients, In: JMIR Human Factors, doi:10.2196/49647

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