132 related articles for article (PubMed ID: 35819379)
1. Health Technology and Big Data: Social Licence, Trust and the Law.
Richards B; Scheibner J
J Law Med; 2022 Jun; 29(2):388-399. PubMed ID: 35819379
[TBL] [Abstract][Full Text] [Related]
2. The social licence for data-intensive health research: towards co-creation, public value and trust.
Muller SHA; Kalkman S; van Thiel GJMW; Mostert M; van Delden JJM
BMC Med Ethics; 2021 Aug; 22(1):110. PubMed ID: 34376204
[TBL] [Abstract][Full Text] [Related]
3. Perspectives of Australian policy-makers on the potential benefits and risks of technologically enhanced communicable disease surveillance - a modified Delphi survey.
Degeling C; Johnson J; Gilbert GL
Health Res Policy Syst; 2019 Apr; 17(1):35. PubMed ID: 30947721
[TBL] [Abstract][Full Text] [Related]
4. Research Stakeholders' Views on Benefits and Challenges for Public Health Research Data Sharing in Kenya: The Importance of Trust and Social Relations.
Jao I; Kombe F; Mwalukore S; Bull S; Parker M; Kamuya D; Molyneux S; Marsh V
PLoS One; 2015; 10(9):e0135545. PubMed ID: 26331716
[TBL] [Abstract][Full Text] [Related]
5. Digital health: meeting the ethical and policy challenges.
Vayena E; Haeusermann T; Adjekum A; Blasimme A
Swiss Med Wkly; 2018; 148():w14571. PubMed ID: 29376547
[TBL] [Abstract][Full Text] [Related]
6. Governance Through Privacy, Fairness, and Respect for Individuals.
Baker DB; Kaye J; Terry SF
EGEMS (Wash DC); 2016; 4(2):1207. PubMed ID: 27141520
[TBL] [Abstract][Full Text] [Related]
7. "A Question of Trust" and "a Leap of Faith"-Study Participants' Perspectives on Consent, Privacy, and Trust in Smart Home Research: Qualitative Study.
Kennedy MR; Huxtable R; Birchley G; Ives J; Craddock I
JMIR Mhealth Uhealth; 2021 Nov; 9(11):e25227. PubMed ID: 34842551
[TBL] [Abstract][Full Text] [Related]
8. Towards trust-based governance of health data research.
Bak MAR; Ploem MC; Tan HL; Blom MT; Willems DL
Med Health Care Philos; 2023 Jun; 26(2):185-200. PubMed ID: 36633724
[TBL] [Abstract][Full Text] [Related]
9. Paths to social licence for tracking-data analytics in university research and services.
White JP; Dennis S; Tomko M; Bell J; Winter S
PLoS One; 2021; 16(5):e0251964. PubMed ID: 34019592
[TBL] [Abstract][Full Text] [Related]
10. Gathering data for decisions: best practice use of primary care electronic records for research.
Canaway R; Boyle DI; Manski-Nankervis JE; Bell J; Hocking JS; Clarke K; Clark M; Gunn JM; Emery JD
Med J Aust; 2019 Apr; 210 Suppl 6(Suppl Suppl 6):S12-S16. PubMed ID: 30927466
[TBL] [Abstract][Full Text] [Related]
11. Co-creating social licence for sharing health and care data.
Fylan F; Fylan B
Int J Med Inform; 2021 May; 149():104439. PubMed ID: 33756337
[TBL] [Abstract][Full Text] [Related]
12. In the shadow of privacy: Overlooked ethical concerns in COVID-19 digital epidemiology.
Ferretti A; Vayena E
Epidemics; 2022 Dec; 41():100652. PubMed ID: 36356477
[TBL] [Abstract][Full Text] [Related]
13. The role of data custodians in establishing and maintaining social licence for health research.
Allen J; Adams C; Flack F
Bioethics; 2019 May; 33(4):502-510. PubMed ID: 30657596
[TBL] [Abstract][Full Text] [Related]
14. Ethical issues in big data: A qualitative study comparing responses in the health and higher education sectors.
Braunack-Mayer A; Carolan L; Street J; Ha T; Fabrianesi B; Carter S
PLoS One; 2023; 18(4):e0282285. PubMed ID: 37097990
[TBL] [Abstract][Full Text] [Related]
15. A qualitative study of big data and the opioid epidemic: recommendations for data governance.
Evans EA; Delorme E; Cyr K; Goldstein DM
BMC Med Ethics; 2020 Oct; 21(1):101. PubMed ID: 33087123
[TBL] [Abstract][Full Text] [Related]
16. Sharing whilst caring: solidarity and public trust in a data-driven healthcare system.
Horn R; Kerasidou A
BMC Med Ethics; 2020 Nov; 21(1):110. PubMed ID: 33143692
[TBL] [Abstract][Full Text] [Related]
17. Personal health information in research: Perceived risk, trustworthiness and opinions from patients attending a tertiary healthcare facility.
Krahe M; Milligan E; Reilly S
J Biomed Inform; 2019 Jul; 95():103222. PubMed ID: 31176040
[TBL] [Abstract][Full Text] [Related]
18. Patients' and public views and attitudes towards the sharing of health data for research: a narrative review of the empirical evidence.
Kalkman S; van Delden J; Banerjee A; Tyl B; Mostert M; van Thiel G
J Med Ethics; 2022 Jan; 48(1):3-13. PubMed ID: 31719155
[TBL] [Abstract][Full Text] [Related]
19. Health Literacy and Health Information Technology Adoption: The Potential for a New Digital Divide.
Mackert M; Mabry-Flynn A; Champlin S; Donovan EE; Pounders K
J Med Internet Res; 2016 Oct; 18(10):e264. PubMed ID: 27702738
[TBL] [Abstract][Full Text] [Related]
20. Using routinely collected health data for surveillance, quality improvement and research: Framework and key questions to assess ethics, privacy and data access.
De Lusignan S; Liyanage H; Di Iorio CT; Chan T; Liaw ST
J Innov Health Inform; 2016 Jan; 22(4):426-32. PubMed ID: 26855276
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]