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Published on: November 26, 2015
Institutional improvements in readability of written informed consent forms sustained post-revised Common Rule
Alison Caballero1, Katherine J Leath1, Jennifer M Gan1
1Center for Health Literacy, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Abstract:
Obtaining informed consent is a fundamental and ethical practice within human subjects' research. Informed consent forms (ICFs) include a large amount of information, much of which may be unfamiliar to research subjects, and the revised Common Rule resulted in several required additions to that language. As limited health literacy impacts many potential subjects, efforts should be made to optimize subjects' ability to read and understand ICFs. In this brief report, we describe an assessment of ICFs at an academic medical center to evaluate longitudinal changes in readability with the introduction and update of a plain language ICF template.
Related Concept Videos
Nurses' Legal Responsibilities I
The legal responsibilities of a nurse regarding informed consent include the following:
Guidelines for Nursing Documentation I
Factual:
The following points emphasize the significance of upholding accurate and unbiased documentation in healthcare.
Legal Guidelines for Documentation
Drug Regulation
Types of Reports III: Telephone and Verbal Reports
Here's an overview of each type:
Telephone Orders
Standards of Care II

