998 related articles for article (PubMed ID: 27083521)
21. Use of electronic patient records for research: views of patients and staff in general practice.
Stevenson F; Lloyd N; Harrington L; Wallace P
Fam Pract; 2013 Apr; 30(2):227-32. PubMed ID: 23132893
[TBL] [Abstract][Full Text] [Related]
22. Comparison of consumers' views on electronic data sharing for healthcare and research.
Kim KK; Joseph JG; Ohno-Machado L
J Am Med Inform Assoc; 2015 Jul; 22(4):821-30. PubMed ID: 25829461
[TBL] [Abstract][Full Text] [Related]
23. Public Views About Involvement in Decision-Making on Health Data Sharing, Access, Use and Reuse: The Importance of Trust in Science and Other Institutions.
Nwebonyi N; Silva S; de Freitas C
Front Public Health; 2022; 10():852971. PubMed ID: 35619806
[TBL] [Abstract][Full Text] [Related]
24. Does an interactive trust-enhanced electronic consent improve patient experiences when asked to share their health records for research? A randomized trial.
Harle CA; Golembiewski EH; Rahmanian KP; Brumback B; Krieger JL; Goodman KW; Mainous AG; Moseley RE
J Am Med Inform Assoc; 2019 Jul; 26(7):620-629. PubMed ID: 30938751
[TBL] [Abstract][Full Text] [Related]
25. Sharing medical data for health research: the early personal health record experience.
Weitzman ER; Kaci L; Mandl KD
J Med Internet Res; 2010 May; 12(2):e14. PubMed ID: 20501431
[TBL] [Abstract][Full Text] [Related]
26. A blockchain-enabled sharing platform for personal health records.
Dong Y; Mun SK; Wang Y
Heliyon; 2023 Jul; 9(7):e18061. PubMed ID: 37496910
[TBL] [Abstract][Full Text] [Related]
27. Patient and public views about the security and privacy of Electronic Health Records (EHRs) in the UK: results from a mixed methods study.
Papoutsi C; Reed JE; Marston C; Lewis R; Majeed A; Bell D
BMC Med Inform Decis Mak; 2015 Oct; 15():86. PubMed ID: 26466787
[TBL] [Abstract][Full Text] [Related]
28. Patient Perspectives About Decisions to Share Medical Data and Biospecimens for Research.
Kim J; Kim H; Bell E; Bath T; Paul P; Pham A; Jiang X; Zheng K; Ohno-Machado L
JAMA Netw Open; 2019 Aug; 2(8):e199550. PubMed ID: 31433479
[TBL] [Abstract][Full Text] [Related]
29. Public involvement in chronic respiratory diseases research: A qualitative study of patients', carers' and citizens' perspectives.
Areia M; Dias LP; Matos P; Figueiredo D; Neves AL; da Costa ED; Loureiro CC; Boechat JL; Reis AB; Simões P; Taborda-Barata L; Fonseca JA; Sá-Sousa A; Jácome C
Health Expect; 2024 Feb; 27(1):e13917. PubMed ID: 38375962
[TBL] [Abstract][Full Text] [Related]
30. An Assessment of Perspectives and Concerns Among Research Participants of Childbearing Age Regarding the Health-Relatedness of Data, Online Data Privacy, and Donating Data to Researchers: Survey Study.
Hendricks-Sturrup R; Lu CY
J Med Internet Res; 2023 Mar; 25():e41937. PubMed ID: 36897637
[TBL] [Abstract][Full Text] [Related]
31. Trust Me, I'm a Doctor: Examining Changes in How Privacy Concerns Affect Patient Withholding Behavior.
Walker DM; Johnson T; Ford EW; Huerta TR
J Med Internet Res; 2017 Jan; 19(1):e2. PubMed ID: 28052843
[TBL] [Abstract][Full Text] [Related]
32. Patients' Perceptions of Different Information Exchange Mechanisms: An Exploratory Study in the United States.
Esmaeilzadeh P
Methods Inf Med; 2020 Aug; 59(4-05):162-178. PubMed ID: 33618421
[TBL] [Abstract][Full Text] [Related]
33. Opening a "Can of Worms" to Explore the Public's Hopes and Fears About Health Care Data Sharing: Qualitative Study.
Lounsbury O; Roberts L; Goodman JR; Batey P; Naar L; Flott KM; Lawrence-Jones A; Ghafur S; Darzi A; Neves AL
J Med Internet Res; 2021 Feb; 23(2):e22744. PubMed ID: 33616532
[TBL] [Abstract][Full Text] [Related]
34. The Costs of Anonymization: Case Study Using Clinical Data.
Pilgram L; Meurers T; Malin B; Schaeffner E; Eckardt KU; Prasser F;
J Med Internet Res; 2024 Apr; 26():e49445. PubMed ID: 38657232
[TBL] [Abstract][Full Text] [Related]
35. Privacy, confidentiality, security and patient safety concerns about electronic health records.
Bani Issa W; Al Akour I; Ibrahim A; Almarzouqi A; Abbas S; Hisham F; Griffiths J
Int Nurs Rev; 2020 Jun; 67(2):218-230. PubMed ID: 32314398
[TBL] [Abstract][Full Text] [Related]
36. Adding dynamic consent to a longitudinal cohort study: A qualitative study of EXCEED participant perspectives.
Wallace SE; Miola J
BMC Med Ethics; 2021 Feb; 22(1):12. PubMed ID: 33563268
[TBL] [Abstract][Full Text] [Related]
37. Dynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical research.
Williams H; Spencer K; Sanders C; Lund D; Whitley EA; Kaye J; Dixon WG
JMIR Med Inform; 2015 Jan; 3(1):e3. PubMed ID: 25586934
[TBL] [Abstract][Full Text] [Related]
38. Attitudes towards Personal Genomics and Sharing of Genetic Data among Older Swiss Adults: A Qualitative Study.
Mählmann L; Schee Gen Halfmann S; von Wyl A; Brand A
Public Health Genomics; 2017; 20(5):293-306. PubMed ID: 29414817
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Information sharing via electronic health records in team-based care: the patient perspective.
Sanyer O; Butler JM; Fortenberry K; Webb-Allen T; Ose D
Fam Pract; 2021 Jul; 38(4):468-472. PubMed ID: 33684209
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
