Understanding the risks in participating in a clinical trial and agreeing to participate is known as ________.
A) the placebo effect
B) the drug affect
C) informed consent
D) drug-drug interaction
E) a double-blind study

Question

Quizplus · Accepted Answer

Informed consent is the process of fully understanding the risks and benefits of participating in a clinical trial and giving voluntary consent to participate. The placebo effect refers to the perceived benefits of a treatment even if it is a placebo. The drug effect refers to the actual effects of a drug. Drug-drug interaction refers to the way drugs can interact with each other in the body. A double-blind study is a research design in which neither the participant nor the researcher knows which group is receiving the treatment or placebo.

Understanding the Risks in Participating in a Clinical Trial and Agreeing