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Category: Blinding in a research. Blinding is the process in a research study of hiding information about which treatment a patient receives. Articles are arranged by date with the most recent entries at the top. You can find the theme and closely related categories and other resources at the bottom of this page.
Stats: Breaking the blind (July 29, 2004). Someone asked an interesting question on the IRBForum today. Under what circumstances should the blinding for a trial be broken when an unexpected Serious Adverse Event (SAE) occurs?
Stats: Unblinding at the end of a study (November 1, 2004). When a study a placebo controlled study is completed, patients in both arms of the study are often offered the active drug at the end of the study at no cost as a way of thanking them for their participation. But some researchers want to continue to measure long term outcomes (outcomes that extend beyond the placebo phase of the study), so they will not reveal to the patients whether they received the active medication or placebo. This raises some difficult ethical issues. Here are a few references on this controversy that I saw on the IRBForum.
Stats: Withholding information (November 28, 2005). A recent query on the IRB Forum asked about a pilot study. The goal of the pilot study was to see if different ways of presenting the materials would lead to an improvement in the response rate among participants. The researchers wanted to withhold information about the purpose of the pilot study from the participants because it might bias their response. The writer of the query was a member of the IRB that wanted some comments about whether it is okay to withhold this information and if patients should be told if they are participating in the pilot phase of the research.
Theme and closely related categories:
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This webpage was written by Steve Simon on 2007-06-04, edited by Steve Simon, and was last modified on 2008-07-08. Send feedback to ssimon at cmh dot edu or click on the email link at the top of the page.