How Should We Communicate the Likelihood of Risks to Inform Decisions about Consent?

IRB: Ethics & Human Research 30 (4):15-18 (2008)
  Copy   BIBTEX

Abstract

Providing understandable information about risks of participation in research is required for informed consent. However, there are no evidence-based guidelines for investigators and members of institutional review boards on how best to do this. A review of literature suggests that, contrary to common practice, simple frequencies with a common denominator rather than probabilistic words should be used to describe the likelihood of risks whenever possible

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 92,813

External links

  • This entry has no external links. Add one.
Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

Similar books and articles

Limits to research risks.F. G. Miller & S. Jofe - 2009 - Journal of Medical Ethics 35 (7):445-449.
Ethical Concerns About Relapse Studies.Adil E. Shamoo & Timothy J. Keay - 1996 - Cambridge Quarterly of Healthcare Ethics 5 (3):373.
Can informed consent to research be adapted to risk?Danielle Bromwich & Annette Rid - 2015 - Journal of Medical Ethics 41 (7):521-528.
Ethical Aspects of Human Subject Research in Biomedicine.David Bruce Fletcher - 1984 - Dissertation, University of Illinois at Urbana-Champaign

Analytics

Added to PP
2015-02-05

Downloads
0

6 months
0

Historical graph of downloads

Sorry, there are not enough data points to plot this chart.
How can I increase my downloads?

Citations of this work

No citations found.

Add more citations

References found in this work

No references found.

Add more references