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Risks and Benefits, Research Involving Persons at Risk for Impaired Decision Making

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Air date: Wednesday, October 22, 2014, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 278 (66 Live, 212 On-demand)
Category: Bioethics
Runtime: 03:03:22
Description: Ethical and Regulatory Aspects of Clinical Research - Session 4

The Department of Bioethics offers this seven to eight week course annually each fall. The course is designed to provide an overview of the important issues in the ethics of human subject research for clinical investigators and others who participate in the conduct of research and is open to the entire NIH community as well as to those from outside NIH. Topics include the history of human subject research ethics, principles and guidelines, study design, subject recruitment, informed consent, and international research. The course is open to the entire NIH community as well as to those from outside NIH. The recommended textbook is Ethical and Regulatory Aspects of Clinical Research, edited by Emanuel et al (Johns Hopkins University Press). The course is taught by guest faculty and faculty members from the National Institutes of Health. This is a required academic program for Bioethics fellows.

Risks and Benefits
Dave Wendler, PhD NIH Clinical Center Department of Bioethics

Research Involving Persons at Risk for Impaired Decision-Making
Scott Kim MD PhD
NIH Clinical Center Department of Bioethics

Participant panel
NLM Title: Ethical and regulatory aspects of clinical research. Session 4, Risks and benefits, research involving persons at risk for impaired decision making / Dave Wendler, Scott Kim.
Author: Wendler, David.
Kim, Scott Y H.
National Institutes of Health (U.S.),
Publisher:
Abstract: (CIT): Ethical and Regulatory Aspects of Clinical Research - Session 4 The Department of Bioethics offers this seven to eight week course annually each fall. The course is designed to provide an overview of the important issues in the ethics of human subject research for clinical investigators and others who participate in the conduct of research and is open to the entire NIH community as well as to those from outside NIH. Topics include the history of human subject research ethics, principles and guidelines, study design, subject recruitment, informed consent, and international research. The course is open to the entire NIH community as well as to those from outside NIH. The recommended textbook is Ethical and Regulatory Aspects of Clinical Research, edited by Emanuel et al (Johns Hopkins University Press). The course is taught by guest faculty and faculty members from the National Institutes of Health. This is a required academic program for Bioethics fellows.
Subjects: Human Experimentation--ethics
Mental Competency
Principal Component Analysis--methods
Research Subjects
Risk Assessment--methods
Publication Types: Lecture
Webcast
 
NLM Classification: W 20.55.H9
NLM ID: 101645899
CIT Live ID: 14703
Permanent link: https://videocast.nih.gov/watch=14703

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