As noted in a recent IRB Research News and Tips blog item, the revised Common Rule will require some changes to the current way we present and document key elements of informed consent information. We have yet to hear specifics about how those new requirements, slated to take effect in January 2018, are to be […]
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We’re still thinking about informed consent processes and forms here
As we gear up for the implementation of the revised Common Rule, slated for January 2018, we’re still thinking about ways to make the informed consent process more meaningful for and understandable to potential subjects. The revised rule includes a requirement that the informed consent “begin with a concise and focused presentation of the key […]
Closure form enrollment tips
We’ve noticed a few trends on reporting enrollment on study closure forms that we’re hoping to nip in the bud: – When listing the total number of people who enrolled in your study, please be sure to include everybody who signed a consent form, even if they failed screening or didn’t actually participate in the […]
New CRS blog quiz is available
The 3rd quarter blog quiz, that will earn you 0.5 hours of Certified Research Specialist Elective credit, is now live. Go to learnondemand.org and type “IRB” into the search box at upper right to access the quiz. Yes, you’ll have around 3 full months to complete this quiz to earn your credit. However, remember how […]
Simplifying informed consent language
A couple of things happened recently that got us thinking about the IRB approval criterion that requires informed consent information to be provided “in language understandable to the subject.” First, we prereviewed some industry study consent forms that were between 20 and 40 single-spaced pages, full of big words about serious disease. If I had […]
Searching the blogs
Q. How can I search for a specific blog item that I know I’ve seen, but I don’t know when? A. Short answer: If you know of a way, do let us know, because we haven’t been able to figure one out. Long answer: Someone had a great idea that we thought we’d share. If […]
New Requirements for Registration and Journal Publication Loom
The International Committee of Medical Journal Editors has started to implement requirements related to sharing individual patient data in manuscripts that report clinical trial results. Beginning July 1, 2018, all manuscripts submitted to ICMJE journals that report clinical trial results must contain a data sharing statement. Clinical trials that begin enrolling participants January 1, 2019, or later must […]
What do IRB members need to know about study design?
The Journal of Medical Ethics blog has a recent entry addressing findings of a study that examined the extent to which IRB members were familiar with some basic study design concepts. (In summary: not very familiar.) The blog entry author writes that she would expect IRB members to know enough about research design to be […]
Remember — neonates also count as subjects!
Many studies involving pregnant women also collect information about the pregnancy outcome. These studies can include both interventional and chart review studies. If you work in this kind of research, please remember that if you collect anything about the newborn, such as gestational age at birth, length, weight, Apgar score, etc., the newborn then meets the […]
PRIM&R director comments about new Common Rule’s informed consent requirements
It seems as though everyone involved in human subject protections struggles with the informed consent process. The desire to provide complete information to subjects can collide with a need to keep informed consent forms and processes simple and understandable. Eliza Hurley, director of the research professional organization Public Responsibility in Medicine and Research (PRIM&R), recently […]