A system and methods for creating electronic informed consent documents regarding a healthcare-related research study. Such informed consent documents can include multimedia content to help the prospective participants make an informed decision as to whether or not to participate in the study. In addition to providing easy to understand information about the study, the system can allow prospective participants to store questions and notes, to take one or more tests to assess their understanding of the study, and to walk through a set of psychological, physical, and environmental issues that can help them better assess whether to participate in the study.
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