National survey of British public's views on use of identifiable medical data by the National Cancer Registry.
about
The risk of re-identification versus the need to identify individuals in rare disease researchPatient and public views about the security and privacy of Electronic Health Records (EHRs) in the UK: results from a mixed methods study.Sharing my health data: a survey of data sharing preferences of healthy individualsDynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical researchPerspectives on neurological patient registries: a literature review and focus group studyPatient and public attitudes towards informed consent models and levels of awareness of Electronic Health Records in the UKIncreasing value and reducing waste in biomedical research regulation and managementNavigating legal constraints in clinical data warehousing: a case study in personalized medicineThe acceptability of conducting data linkage research without obtaining consent: lay people's views and justifications.Real-world data in the United Kingdom: opportunities and challengesCommunity attitudes to the collection and use of identifiable data for health research--is it an invasion of privacy?The Florey Adelaide Male Ageing Study (FAMAS): design, procedures & participants.The impact of consent on observational research: a comparison of outcomes from consenters and non consenters to an observational study.The perceived impact of location privacy: a web-based survey of public health perspectives and requirements in the UK and CanadaQuality indicators and quality assessment in child healthSharing medical data for health research: the early personal health record experience.Saudi views on consenting for research on medical records and leftover tissue samples.Are cancer registries unconstitutional?Involving users in the design of a randomised controlled trial of an intervention to promote early presentation in breast cancer: qualitative studyA randomised controlled trial to compare opt-in and opt-out parental consent for childhood vaccine safety surveillance using data linkage: study protocol.Recruitment of representative samples for low incidence cancer populations: do registries deliver?Survey of patient and public perceptions of electronic health records for healthcare, policy and research: study protocol.Parent perspectives on consent for the linkage of data to evaluate vaccine safety: a randomised trial of opt-in and opt-out consent.Overcoming barriers to recruitment in health research.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).Population attitudes towards research use of health care registries: a population-based survey in FinlandThe ethics of withdrawal: the case of follow-up from first-in-human clinical trials.Cancer survivorship monitoring systems for the collection of patient-reported outcomes: a systematic narrative review of international approaches.A critique of the regulation of data science in healthcare research in the European Union.Alternatives to project-specific consent for access to personal information for health research: what is the opinion of the Canadian public?Identifying and hurdling obstacles to translational research.Recruiting participants for injury studies in emergency departments.Assessing the impact of the requirement for explicit consent in a hospital-based stroke study.Extracting information from hospital records: what patients think about consentPatient and public views on electronic health records and their uses in the United kingdom: cross-sectional surveyJoint replacement recipients' views about health information privacy.Low risk research using routinely collected identifiable health information without informed consent: encounters with the Patient Information Advisory Group.Feasibility and cost of obtaining informed consent for essential review of medical records in large-scale health services research.Health systems performance and cancer outcomes.The impact of privacy and confidentiality laws on the conduct of clinical trials.
P2860
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P2860
National survey of British public's views on use of identifiable medical data by the National Cancer Registry.
description
2006 nî lūn-bûn
@nan
2006 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
National survey of British pub ...... the National Cancer Registry.
@ast
National survey of British pub ...... the National Cancer Registry.
@en
type
label
National survey of British pub ...... the National Cancer Registry.
@ast
National survey of British pub ...... the National Cancer Registry.
@en
prefLabel
National survey of British pub ...... the National Cancer Registry.
@ast
National survey of British pub ...... the National Cancer Registry.
@en
P2860
P50
P1433
P1476
National survey of British pub ...... the National Cancer Registry.
@en
P2093
National Cancer Registry
P2860
P304
P356
10.1136/BMJ.38805.473738.7C
P407
P577
2006-04-28T00:00:00Z