Background Deferred consent is used to recruit patients in emergency research, when informed consent cannot be obtained prior to enrolment. This model of consent allows studies to recruit larger numbers of participants, especially where a surrogate-decision maker may be unavailable to provide consent. Whilst deferred consent offers the potential to promote trial diversity by including under-served groups, it is ethically complex and views about its use amongst these populations require further exploration. The aim of this article is to build upon recent initiatives to improve inclusivity in trials, such as the NIHR INCLUDE project, and consider whether trials methodology research is inclusive, focusing on ethnic minority populations’ attit...
Despite substantial awareness that certain groups (e.g. ethnic minorities) are under-represented and...
Background: People from ethnic minorities are reported to have higher rates of physical illness (di...
Although the controversy over the lack of consent in fetal-tissue clinical trials is relatively new,...
Background Deferred consent is used to recruit patients in emergency research, when informed consen...
Abstract Background Deferred consent is used to recruit patients in emergency research, when informe...
Research has shown that there continues to be insufficient recruitment of minorities in clinical tri...
Background Patients with acute conditions often lack the capacity to provide informed consent, and ...
Although extensive research addresses minorities’ low participation in clinical research, most focus...
It is widely claimed that racial and ethnic minorities, especially in the US, are less willing than ...
Background: Informed consent is considered a fundamental requirement for participation in trials, ye...
BACKGROUND: Despite substantial awareness that certain groups (e.g. ethnic minorities) are under-rep...
Informed consent is an essential requirement prior to clinical trial participation, however some ‘vu...
Background: Previous health research has often explicitly excluded individuals from minority ethni...
Despite substantial awareness that certain groups (e.g. ethnic minorities) are under-represented and...
Background: People from ethnic minorities are reported to have higher rates of physical illness (di...
Although the controversy over the lack of consent in fetal-tissue clinical trials is relatively new,...
Background Deferred consent is used to recruit patients in emergency research, when informed consen...
Abstract Background Deferred consent is used to recruit patients in emergency research, when informe...
Research has shown that there continues to be insufficient recruitment of minorities in clinical tri...
Background Patients with acute conditions often lack the capacity to provide informed consent, and ...
Although extensive research addresses minorities’ low participation in clinical research, most focus...
It is widely claimed that racial and ethnic minorities, especially in the US, are less willing than ...
Background: Informed consent is considered a fundamental requirement for participation in trials, ye...
BACKGROUND: Despite substantial awareness that certain groups (e.g. ethnic minorities) are under-rep...
Informed consent is an essential requirement prior to clinical trial participation, however some ‘vu...
Background: Previous health research has often explicitly excluded individuals from minority ethni...
Despite substantial awareness that certain groups (e.g. ethnic minorities) are under-represented and...
Background: People from ethnic minorities are reported to have higher rates of physical illness (di...
Although the controversy over the lack of consent in fetal-tissue clinical trials is relatively new,...