4 Common Myths About Clinical Trials

Sponsored by Merck Clinical trials are research studies that are designed to learn more about how our bodies respond to investigational medicines. Any medicine, vaccine, medical device or procedure that is approved for public use has first been studied in a clinical trial. It is important to include participants from various backgrounds so we can help ensure the data we receive from the clinical trial reflects the diversity of the population we hope to serve. However, misunderstandings about clinical trials still prevent many people from taking steps to learn about and participate in clinical research. In this article, we discuss common myths surrounding clinical trials and explore the impact of increased participation within underserved communities.  Myth #1: Participating in a clinical trial means being treated like a “guinea pig.” In many communities of color, there is distrust for the medical community and clinical research because people’s race and socioeconomic status have been used against them. However, it is important to know that clinical trials follow strict ethical guidelines and regulatory standards designed to help protect participants’ rights and safety. Before enrolling in a trial, participants receive detailed information about the study’s purpose, procedures, potential risks, and benefits, and have the...