Objectives To establish the views of research volunteers on the consent process; to explore their views on the consent process in different research scenarios; to inform debate on emerging mod-els of consent for participation in research. Design, Setting and Participants 2,308 adult volunteers from the TwinsUK Registry (www.twinsuk.ac.uk) completed an on-line survey about their views on the consent process for use of their DNA and medical infor-mation in research. Their views on the re-consenting process in different scenarios were assessed. Results The majority of volunteers preferred to be informed of the identity of the main researcher of a study in which they are participating, which is contrary to current practice. Over 80 % were willi...
The 100,000 Genomes Project (100kGP)—a hybrid clinical-research initiative—was set up to analyse who...
Context Biobanks are important resources which enable large-scale genomic research with human sample...
Background: Recent scandals relating to the unconsented retention and use of human organs in the UK ...
<div><p>Objectives</p><p>To establish the views of research volunteers on the consent process; to ex...
This is the final version of the article. Available from the publisher via the DOI in this record.OB...
OBJECTIVE: A mixed-methods study exploring the UK general public's views towards consent for the use...
Item does not contain fulltextBACKGROUND: Population based genetics studies are dependent on large n...
Background/Aims: To understand patient views about consent for secondary use and sharing of genetic ...
\(\bf Background:\) Appropriate information and consent has been one of the most intensely discussed...
Much is known about patient attitudes to ethical and legal questions in the context of biobanking, p...
BackgroundClinical genomic implementation studies pose challenges for informed consent. Consent form...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
Consent forms are the principal method for obtaining informed consent from biomedical research parti...
Research participants ’ perceptions and views on consent for biobank research: a review of empirical...
Much is known about patient attitudes to ethical and legal questions in the context of biobanking, p...
The 100,000 Genomes Project (100kGP)—a hybrid clinical-research initiative—was set up to analyse who...
Context Biobanks are important resources which enable large-scale genomic research with human sample...
Background: Recent scandals relating to the unconsented retention and use of human organs in the UK ...
<div><p>Objectives</p><p>To establish the views of research volunteers on the consent process; to ex...
This is the final version of the article. Available from the publisher via the DOI in this record.OB...
OBJECTIVE: A mixed-methods study exploring the UK general public's views towards consent for the use...
Item does not contain fulltextBACKGROUND: Population based genetics studies are dependent on large n...
Background/Aims: To understand patient views about consent for secondary use and sharing of genetic ...
\(\bf Background:\) Appropriate information and consent has been one of the most intensely discussed...
Much is known about patient attitudes to ethical and legal questions in the context of biobanking, p...
BackgroundClinical genomic implementation studies pose challenges for informed consent. Consent form...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
Consent forms are the principal method for obtaining informed consent from biomedical research parti...
Research participants ’ perceptions and views on consent for biobank research: a review of empirical...
Much is known about patient attitudes to ethical and legal questions in the context of biobanking, p...
The 100,000 Genomes Project (100kGP)—a hybrid clinical-research initiative—was set up to analyse who...
Context Biobanks are important resources which enable large-scale genomic research with human sample...
Background: Recent scandals relating to the unconsented retention and use of human organs in the UK ...