Informed consent for participation in a clinical trial requires that researchers inform the subject whether they will be in the control group or experimental group.

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Informed consent requires explaining the nature of the study, potential risks, benefits, and the subject's rights, including confidentiality and voluntary participation. However, specific group assignments (control or experimental) may not be disclosed, especially in blinded studies, to maintain the integrity of the research.

Informed Consent for Participation in a Clinical Trial Requires That