Informed Consent and Assent Decisions by Persons with Dementia and their Legally Designated Representatives.
نویسندگان
چکیده
منابع مشابه
The conduct of Canadian researchers and institutional review boards regarding substituted consent for research.
As the population ages worldwide, a growing number of individuals suffer from diseases that impair their decisionmaking capacity.1 Over the years, researchers around the world have intensified their efforts to identify the causes of these diseases, develop effective treatments to slow their progression, and further our understanding of their impact on affected individuals and their families.2 A...
متن کاملBrief report on the experience of using proxy consent for incapacitated adults.
The Medicines for Human Use (Clinical Trials) Regulations 2004, which came into force in the UK in May 2004, cover the conduct of clinical trials on medicinal products. They allow a legal representative (a person not connected with the conduct of the trial) to consent to the participation of incompetent adults in medical research. Currently, very little is known about how such representatives w...
متن کاملInformed Consent Process: Foundation of the Researcher-participant Bond
Consenting to participate in a clinical research study after being properly and correctly informed upholds the basic ethical principle of "autonomy" in human research. The informed consent is a process by which the physician sensitizes the patient about the nature, procedures, risks benefits, treatment schedules, etc of the study in a language that is non-technical and understandable by the stu...
متن کاملOverview of European legislation on informed consent for neonatal research.
Euricon, a European Union funded study, had the objective of examining the issue of obtaining informed consent for neonatal research across Europe. As part of that project, legal representatives from these countries (see acknowledgements) were invited to a colloquium to report, discuss, and analyse European legal frameworks governing informed consent for neonatal research. The first author (PDV...
متن کاملReporting ethical processes in two Indian journals.
BACKGROUND In biomedical journals, authors are expected to report if the study was carried out in accordance with international and national ethical guidelines and inform readers if approval from ethics committee was obtained and if written informed consent was taken from the participant or legal guardian. AIMS To determine the proportion of research manuscripts in two pediatric journals publ...
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ورودعنوان ژورنال:
- Journal of empirical research on human research ethics : JERHRE
دوره 2 1 شماره
صفحات -
تاریخ انتشار 2007