Format

Send to

Choose Destination
Nurs Ethics. 2014 Feb;21(1):16-27. doi: 10.1177/0969733013487190. Epub 2013 May 28.

Protecting boundaries of consent in clinical research: implications for improvement.

Author information

1
Loma Linda University, USA.

Abstract

Successful clinical research outcomes are essential for improving patient care. Achieving this goal, however, implies an effective informed consent process for potential research participants. This article traces the development of ethical and legal requirements of informed consent and examines the effectiveness of past and current practice. The authors propose the use of innovative monitoring methodologies to improve outcomes while safeguarding consent relationships and activities. Additional rigorous research will help direct policy efforts at standardizing quality improvement processes.

KEYWORDS:

Clinical research; informed consent; quality improvement

PMID:
23715553
DOI:
10.1177/0969733013487190
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Atypon
Loading ...
Support Center