Question
Every time we add regulations to research studies, we influence the design and types of research that can be conducted. Let's hypothetically think of participants
Every time we add regulations to research studies, we influence the design and types of research that can be conducted. Let's hypothetically think of participants who agree to a clinical trial. For this example, let's say the person is terminal and has exhausted all medical options. If they are given a placebo (which is deception) and die - is this putting the person in distress?
As a social science, we often study trauma, which can be very distressing. Although we don't want to distress a subject, it may be necessary. This begs the question (to me) how do we conduct informative research about important issues in our society if we are not allowed to distress the subjects?
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