Informed consent: A clinical trials perspective Journal Article


Authors: Hammer, M. J.; Eckardt, P.; Barton-Burke, M.
Article Title: Informed consent: A clinical trials perspective
Abstract: The primary goal of the thousands of registered trials in cancer research is to extend survival. With evaluation of efficacy, safety, and tolerability, healthcare providers must ensure that the principles described in the Belmont Report are upheld and that patients are truly informed when signing a consent form. In this article, two cases are highlighted, and reasons for participating in clinical trials are discussed. Challenges, such as healthcare literacy, patients' dedication to their healthcare providers, and choosing between multiple trials, are also explored. Copyright 2016 by the Oncology Nursing Society.
Keywords: genetics; clinical trial; case report; biology; cancer research; doctor patient relation; health care personnel; safety; informed consent; ethics; nursing research; comparative effectiveness; human; biology of cancer
Journal Title: Oncology Nursing Forum
Volume: 43
Issue: 6
ISSN: 0190-535X
Publisher: Oncology Nursing Society (ONS)  
Date Published: 2016-11-01
Start Page: 694
End Page: 696
Language: English
DOI: 10.1188/16.onf.694-696
PROVIDER: scopus
PUBMED: 27768140
PMCID: PMC5637387
DOI/URL:
Notes: Article -- Export Date: 2 November 2016 -- Source: Scopus
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