Research involving vulnerable population of mentally impaired persons is raising considerable controversies from its very beginnings. These controversies are created around everlasting tensions between two positive duties: the duty to protect vulnerable subjects, and the duty not to deny them potential benefits. Most of the contemporary ethical guidelines and regulations, including most recent revision of the Declaration of Helsinki, permit these researches under certain ethical conditions. The notion of informed consent as a cornerstone of bioethics emerges as essential requisite of moral research. We are presenting some key concepts and safeguards regarding informed consent that researcher needs to be aware off when conducting a research ...
Informed consent procedures for participation in psychiatric genomics research amongst individuals w...
Abstract: This paper describes the legal and ethical as-pects of informed consent, including the req...
Informed consent for clinical research is both a communication process and a document to inform indi...
Research involving vulnerable population of mentally impaired persons is raising considerable contro...
Obtaining informed consent in psychiatry clinical research involving subjects with diminished mental...
Informed and voluntary consent are important aspects when conducting human research and is an area t...
Informed consent refers to the process of giving information, discussing and obtaining permission of...
Informed consent procedures for participation in psychiatric genomics research among individuals wit...
Biomedical research is important for development of science, diagnostics and production of new, effe...
Informed consent process is crucial in any research. The consent is meaningful only when the subject...
Because of concerns about competence and voluntariness, the mentally disordered constitute a vulnera...
This article begins with an in-depth discussion of the UCLA incident followed by the history of prot...
This Note demonstrates that the federal regulations regarding human subject research must provide mo...
Among four basic principles (respect for autonomy, beneficence, non-malfeasance, and justice) which ...
Key words: acute psychiatry; informed consent; participant observation; power dynamics in nursing ca...
Informed consent procedures for participation in psychiatric genomics research amongst individuals w...
Abstract: This paper describes the legal and ethical as-pects of informed consent, including the req...
Informed consent for clinical research is both a communication process and a document to inform indi...
Research involving vulnerable population of mentally impaired persons is raising considerable contro...
Obtaining informed consent in psychiatry clinical research involving subjects with diminished mental...
Informed and voluntary consent are important aspects when conducting human research and is an area t...
Informed consent refers to the process of giving information, discussing and obtaining permission of...
Informed consent procedures for participation in psychiatric genomics research among individuals wit...
Biomedical research is important for development of science, diagnostics and production of new, effe...
Informed consent process is crucial in any research. The consent is meaningful only when the subject...
Because of concerns about competence and voluntariness, the mentally disordered constitute a vulnera...
This article begins with an in-depth discussion of the UCLA incident followed by the history of prot...
This Note demonstrates that the federal regulations regarding human subject research must provide mo...
Among four basic principles (respect for autonomy, beneficence, non-malfeasance, and justice) which ...
Key words: acute psychiatry; informed consent; participant observation; power dynamics in nursing ca...
Informed consent procedures for participation in psychiatric genomics research amongst individuals w...
Abstract: This paper describes the legal and ethical as-pects of informed consent, including the req...
Informed consent for clinical research is both a communication process and a document to inform indi...