Today’s video features Don walking us through what we can expect during an informed consent process in a clinical trial. Before anyone can be enrolled into a clinical trial, a complete informed consent must be given in which the study participant is explained the purpose of the study, the potential benefits of the trial as well as the potential risks and side effects of the clinical trial. Many people may be intimidated by the lengthy paperwork that makes up the informed consent, so this video will hopefully give you a greater understanding of what you can expect when looking at an informed consent form with your study doctor or study coordinator.


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