Implications of therapeutic misconception in clinical research

7 minute read

Clinical research is one of the most valuable efforts in advancing healthcare. Most healthcare professionals understand the importance of clinical research. Additionally, most healthcare providers involved in clinical research are aware of potential clinical risks in research involving human subjects. However, many may not recognize one of the most significant ethical concerns and risks inherent in clinical research, which occurs when patients also participate in research studies. Therapeutic misconception occurs when principal investigators, healthcare providers, and research participants cannot distinguish the differences between medical care and research. When a person agrees to participate in a clinical research study, their status changes from patient to research subject or participant. The care provided to research participants differs in some ways due to the research protocol requirements. Certain services required by the protocol are intended to further the clinical investigation aims. Because of the differences in the care and services provided, a patient’s risks of participating in research may be higher than the risks of clinical care received outside a clinical trial. All parties involved in research—from the investigators to the research staff to the participants—must understand that the goals of medical care and research are different, as are the roles of a clinician and an investigator.

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