Exportar Publicação

A publicação pode ser exportada nos seguintes formatos: referência da APA (American Psychological Association), referência do IEEE (Institute of Electrical and Electronics Engineers), BibTeX e RIS.

Exportar Referência (APA) 
Freitas, C. de., Silva, S., Teles, E. L., Maia, T. & Amorim, M. (2020). Participation in data generation and information sharing: Are patients and carers willing to engage?. In European Journal of Public Health. (pp. v138).: Oxford University Press (OUP).
Exportar Referência (IEEE) 
C. S. Freitas et al.,  "Participation in data generation and information sharing: Are patients and carers willing to engage?", in European Journal of Public Health, Oxford University Press (OUP), 2020, vol. 30, Suppl.5, pp. v138
Exportar BibTeX 
@inproceedings{freitas2020_1713860303084,
	author = "Freitas, C. de. and Silva, S. and Teles, E. L. and Maia, T. and Amorim, M.",
	title = "Participation in data generation and information sharing: Are patients and carers willing to engage?",
	booktitle = "European Journal of Public Health",
	year = "2020",
	editor = "",
	volume = "30, Suppl.5",
	number = "",
	series = "",
	doi = "10.1093/eurpub/ckaa165.370",
	pages = "v138",
	publisher = "Oxford University Press (OUP)",
	address = "",
	organization = "World Federation of Public Health Associations (WFPHA), Italian Society of Hygiene, Preventive Medicine and Public Health (SItI), European Public Health Association (EUPHA)",
	url = "https://academic.oup.com/eurpub"
}
Exportar RIS 
TY  - CPAPER
TI  - Participation in data generation and information sharing: Are patients and carers willing to engage?
T2  - European Journal of Public Health
VL  - 30, Suppl.5
AU  - Freitas, C. de.
AU  - Silva, S.
AU  - Teles, E. L.
AU  - Maia, T.
AU  - Amorim, M.
PY  - 2020
SP  - v138
SN  - 1101-1262
DO  - 10.1093/eurpub/ckaa165.370
UR  - https://academic.oup.com/eurpub
AB  - Health systems are moving towards a personalisation of care. Personalised care relies on data-intensive research, which depends on active participation by citizens in data generation and information sharing. Collecting and sharing one’s data for research can deliver several benefits. However, it also comes at a cost in time and effort that may burden different population subsets to varying degrees. This study aimed to assess patients’ and carers’ willingness to generate and share health data, and its associated factors, to inform the design of inclusive engagement strategies.
ER  -