A primary ethical high ideal for obtaining informed consent entails a prior disclosure of the study’s purpose and design to the participants. It also requires the researcher to divulge comprehensive information pertinent to the research, including the timelines, procedures, incentives offered, right to withdraw from the study, anticipated participation risks, confidentiality levels, and study benefits. Informed consent essentially enhances the participants’ understanding of the subject and willingness to participate. It is important for various ethical reasons. First, it helps meet the principles of beneficence and fairness entitled to human subjects. Second, communicating pertinent information related to the research helps minimize potential harm to the participants. From a procedural standpoint, informed consent is also a key requirement of the Institutional Review Board guidelines.
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