England and Wales are moving toward a model of 'opt out' for use of personal confidential data in health research. Existing research does not make clear how acceptable this move is to the public. While people are typically supportive of health research, when asked to describe the ideal level of control there is a marked lack of consensus over the preferred model of consent (e.g. explicit consent, opt out etc.). This study sought to investigate a relatively unexplored difference between the consent model that people prefer and that which they are willing to accept. It also sought to explore any reasons for such acceptance.A mixed methods approach was used to gather data, incorporating a structured questionnaire and in-depth focus group discu...
Much is known about patient attitudes to ethical and legal questions in the context of biobanking, p...
Objectives To establish the views of research volunteers on the consent process; to explore their vi...
Anonymised data from a 2020 UK survey of public opinion about sharing NHS health data for clinical a...
England and Wales are moving toward a model of ‘opt out’ for use of personal confidential data in he...
England and Wales are moving toward a model of ‘opt out’ for use of personal confidential data in he...
To establish the views of research volunteers on the consent process; to explore their views on the ...
Abstract Background Stigma refers to a distinguishing personal trait that is perceived as or actuall...
Medical research has a long history in the United Kingdom and has generally enjoyed good public supp...
OBJECTIVE: A mixed-methods study exploring the UK general public's views towards consent for the use...
BACKGROUND England operates a National Data Opt-Out (NDOO) for the secondary use of confidential ...
Variation across research ethics boards (REBs) in conditions placed on access to medical records for...
Ethics committees now require that individuals give informed consent to much health services researc...
The General Data Protection Regulation (GDPR) was introduced in 2018 to harmonize data privacy and s...
Not to be quoted without author’s permission Patterns of research governance in the UK are changing ...
Abstract Background Immense volumes of personal healt...
Much is known about patient attitudes to ethical and legal questions in the context of biobanking, p...
Objectives To establish the views of research volunteers on the consent process; to explore their vi...
Anonymised data from a 2020 UK survey of public opinion about sharing NHS health data for clinical a...
England and Wales are moving toward a model of ‘opt out’ for use of personal confidential data in he...
England and Wales are moving toward a model of ‘opt out’ for use of personal confidential data in he...
To establish the views of research volunteers on the consent process; to explore their views on the ...
Abstract Background Stigma refers to a distinguishing personal trait that is perceived as or actuall...
Medical research has a long history in the United Kingdom and has generally enjoyed good public supp...
OBJECTIVE: A mixed-methods study exploring the UK general public's views towards consent for the use...
BACKGROUND England operates a National Data Opt-Out (NDOO) for the secondary use of confidential ...
Variation across research ethics boards (REBs) in conditions placed on access to medical records for...
Ethics committees now require that individuals give informed consent to much health services researc...
The General Data Protection Regulation (GDPR) was introduced in 2018 to harmonize data privacy and s...
Not to be quoted without author’s permission Patterns of research governance in the UK are changing ...
Abstract Background Immense volumes of personal healt...
Much is known about patient attitudes to ethical and legal questions in the context of biobanking, p...
Objectives To establish the views of research volunteers on the consent process; to explore their vi...
Anonymised data from a 2020 UK survey of public opinion about sharing NHS health data for clinical a...