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Summary Points: key component of informed consent to participate in medical research is the understanding that research is not the same as treatment. , studies have found that some research participants do not appreciate important differences between research and treatment, a phenomenon called “therapeutic misconception. ” consistent definition of therapeutic misconception is missing from the literature, and this hinders attempts to define its prevalence or ways to reduce it. paper proposes a new definition and describes how it can be operationalized.
Henderson et al. (Tue,) studied this question.
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