Alternatives to project-specific consent for access to personal information for health research: what is the opinion of the Canadian public?
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Comparison of consumers' views on electronic data sharing for healthcare and researchDeveloping a new model for patient recruitment in mental health services: a cohort study using Electronic Health RecordsPatient and public attitudes towards informed consent models and levels of awareness of Electronic Health Records in the UKA Protocol for the secure linking of registries for HPV surveillancePhysician privacy concerns when disclosing patient data for public health purposes during a pandemic influenza outbreakRespecting donors to biobank research.Alternatives to project-specific consent for access to personal information for health research: insights from a public dialogueConsent for use of personal information for health research: do people with potentially stigmatizing health conditions and the general public differ in their opinions?Sociodemographic data collection for health equity measurement: a mixed methods study examining public opinions.A survey aimed at general citizens of the US and Japan about their attitudes toward electronic medical data handlingParent perspectives on privacy and governance for a pediatric repository of non-biological, research data.Glad you asked: participants' opinions of re-consent for dbGap data submissionSaudi views on consenting for research on medical records and leftover tissue samples.A randomised controlled trial to compare opt-in and opt-out parental consent for childhood vaccine safety surveillance using data linkage: study protocol.Public preferences about secondary uses of electronic health information.The re-identification risk of Canadians from longitudinal demographics.Estimating the re-identification risk of clinical data setsParent perspectives on consent for the linkage of data to evaluate vaccine safety: a randomised trial of opt-in and opt-out consent.Acceptability and perceived barriers and facilitators to creating a national research register to enable 'direct to patient' enrolment into research: the Scottish Health Research Register (SHARE).Strategies for maintaining patient privacy in i2b2.Population attitudes towards research use of health care registries: a population-based survey in FinlandThe importance of purpose: moving beyond consent in the societal use of personal health information.Demographic differences in willingness to provide broad and narrow consent for biobank research.A survey of patient perspectives on the research use of health information and biospecimensParticipant views on consent in cancer genetics research: preparing for the precision medicine era.Joint replacement recipients' views about health information privacy.Public opinion about the importance of privacy in biobank research.Patient informed governance of distributed research networks: results and discussion from six patient focus groups"It's my blood": ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants.Use of electronic patient records for research: views of patients and staff in general practice.Stakeholders' views on data sharing in multicenter studies.Stepping Up to the Plate: An Agenda for Research and Policy Action on Electronic Medical Records in Canadian Primary Healthcare.Patients' views about the use of their personal information from general practice medical records in health research: a qualitative study in Ireland.Preferences for opt-in and opt-out enrollment and consent models in biobank research: a national survey of Veterans Administration patients.Patient preferences toward an interactive e-consent application for research using electronic health records.The research participant perspective related to the conduct of genomic cohort studies: A systematic review of the quantitative literature.Investigating the Extent to Which Patients Should Control Access to Patient Records for Research: A Deliberative Process Using Citizens' Juries.
P2860
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P2860
Alternatives to project-specific consent for access to personal information for health research: what is the opinion of the Canadian public?
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh
2007年學術文章
@zh-hant
name
Alternatives to project-specif ...... pinion of the Canadian public?
@ast
Alternatives to project-specif ...... pinion of the Canadian public?
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type
label
Alternatives to project-specif ...... pinion of the Canadian public?
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Alternatives to project-specif ...... pinion of the Canadian public?
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prefLabel
Alternatives to project-specif ...... pinion of the Canadian public?
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Alternatives to project-specif ...... pinion of the Canadian public?
@en
P2093
P2860
P356
P1476
Alternatives to project-specif ...... pinion of the Canadian public?
@en
P2093
Cathy Charles
David Northrup
Donald J Willison
Julia Abelson
Marilyn Swinton
P2860
P304
P356
10.1197/JAMIA.M2457
P577
2007-08-21T00:00:00Z