Empirical studies of ethical issues, which have increased in number and scope in recent years, may themselves raise both practical and ethical issues. One example of such an issue is the question of who may be legitimately enrolled in studies of decision-making capacity; must all partici-pants in studies of consent capacity have capacity to con-sent? This question may pose a ‘‘Catch-22’’: For example, if some of the participants in a study of consent capacity are deemed by a particular standard to be incapable of consent. In weighing the risks and benefits of studies of consent capacity, how should reviewers consider the context of ac-tual versus hypothetical trials for which the participant’s consent is being sought? Here, we explore these...
Background Biomedical research increasingly relies on long-term studies involving use and re-use of...
Decision-making capacity for treatment and research raises complex conceptual issues. Given the fact...
Informed consent is an essential requirement prior to clinical trial participation, however some ‘vu...
With the ever increasing focus on collecting and conducting research in to ‘Big Data’, there is grow...
Population-level biomedical research has become crucial to the health system’s ability to improve th...
This article addresses two areas of continuing controversy about consent in clinical research: the q...
Subjects who lack capacity to give consent are common in dementia research, emergency research, and ...
\(\bf Background:\) Appropriate information and consent has been one of the most intensely discussed...
Population-level biomedical research has become crucial to the health system’s ability to improve th...
The biobank consent debate is one with deeply held convictions on both the ‘broad’ and ‘specific’ si...
This chapter has two connected aims. First, I argue that we can best understand the scope and limits...
Obtaining informed consent in psychiatry clinical research involving subjects with diminished mental...
In a recent article, I argued that Ploug and Holm’s ‘meta-consent’ proposal should be rejected for b...
With the growth in recent years of studies of decisional ca-pacity for research among people with sc...
Since its inception as an international requirement to protect patients and healthy volunteers takin...
Background Biomedical research increasingly relies on long-term studies involving use and re-use of...
Decision-making capacity for treatment and research raises complex conceptual issues. Given the fact...
Informed consent is an essential requirement prior to clinical trial participation, however some ‘vu...
With the ever increasing focus on collecting and conducting research in to ‘Big Data’, there is grow...
Population-level biomedical research has become crucial to the health system’s ability to improve th...
This article addresses two areas of continuing controversy about consent in clinical research: the q...
Subjects who lack capacity to give consent are common in dementia research, emergency research, and ...
\(\bf Background:\) Appropriate information and consent has been one of the most intensely discussed...
Population-level biomedical research has become crucial to the health system’s ability to improve th...
The biobank consent debate is one with deeply held convictions on both the ‘broad’ and ‘specific’ si...
This chapter has two connected aims. First, I argue that we can best understand the scope and limits...
Obtaining informed consent in psychiatry clinical research involving subjects with diminished mental...
In a recent article, I argued that Ploug and Holm’s ‘meta-consent’ proposal should be rejected for b...
With the growth in recent years of studies of decisional ca-pacity for research among people with sc...
Since its inception as an international requirement to protect patients and healthy volunteers takin...
Background Biomedical research increasingly relies on long-term studies involving use and re-use of...
Decision-making capacity for treatment and research raises complex conceptual issues. Given the fact...
Informed consent is an essential requirement prior to clinical trial participation, however some ‘vu...