Reference : The patients’ perspective on access to and use of Personal Health Records

	Document type :	Scientific congresses, symposiums and conference proceedings : Unpublished conference
	Discipline(s) :	Human health sciences : Public health, health care sciences & services
	Focus Areas :	Sustainable Development
	To cite this reference:	http://hdl.handle.net/10993/44836

Title :	The patients’ perspective on access to and use of Personal Health Records
Language :	English
Author, co-author :	Paccoud, Ivana [University of Luxembourg > Faculty of Humanities, Education and Social Sciences (FHSE) > Department of Social Sciences (DSOC) >]
	Baumann, Michèle [University of Luxembourg > Faculty of Language and Literature, Humanities, Arts and Education (FLSHASE) > >]
	Le Bihan, Etienne [University of Luxembourg > Faculty of Humanities, Education and Social Sciences (FHSE) > Department of Social Sciences (DSOC) >]
	Pétré, Benoit []
	Breinbauer, Mareike []
	Böhme, Philipp []
	Chauvel, Louis [University of Luxembourg > Faculty of Humanities, Education and Social Sciences (FHSE) > Department of Social Sciences (DSOC) >]
	Leist, Anja [University of Luxembourg > Faculty of Humanities, Education and Social Sciences (FHSE) > Department of Social Sciences (DSOC) >]
Publication date :	2020
Peer reviewed :	No
On invitation :	Yes
Audience :	International
Event name :	SAPHIRe Online Workshop "Access to health data - the role of regional actors, gatekeepers, providers and individuals"
Event date :	29 October 2020
Event organizer :	H2020 Securing the Adoption of Personalised Health in Regions (SAPHIRe) consortium
Event place (city) :	virtual
Event country :	Belgium
Keywords :	[en] personalised health ; socio-economic inequalities ; UTAUT model ; technology acceptance ; data privacy ; Greater Region ; Dossier de Soins Partagé ; health inequalities
Abstract :	[en] We present the patients' perspective regarding the use of Personal Health Records, and give insights on patients' characteristics, such as socioeconomic and behavioural factors, that are associated with the access to and use of Personal Health Records. The findings come from the INTERREG APPS project that investigated preferences for and intention to use Personal Health Records in four cross-border regions, in Lorraine/France, Luxembourg, Rhineland-Palatinate and Saarland/Germany, and Wallonia/Belgium.
Research centres :	Integrative Research Unit: Social and Individual Development (INSIDE) > PEARL Institute for Research on Socio-Economic Inequality (IRSEI)
Funders :	University of Luxembourg - UL
Name of the research project :	Projet cofinancé par Fonds Européen Développement Régional programme INTERREG V A Grande Région
Target :	Researchers ; Professionals ; General public
Permalink :	http://hdl.handle.net/10993/44836

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