Experience has shown that there can be important differences in how people of diverse groups respond to medical products.
FREE CLINICAL TRIALS FOR HURNIA NEAR DALLAS TX TRIAL
Before joining a study, you should understand your rights as a clinical trial participant.
Your participation can impact health care for the public good. As a patient, participation in a clinical trial can help you access new treatments still in research stages. It is important for patients in those populations who are more likely to be treated for a condition to be included in a trial. Clinical trials help advance science and discover new therapies.
Certain populations can be more at risk for certain diseases – such as diabetes and heart disease – than others.Food and Drug Administration (FDA) explicitly states the importance of diversity in clinical studies: This is especially important for certain populations, such as adults aged 75 years or older, people from different ethnic and racial groups, people from different socioeconomic backgrounds, and other underrepresented communities such as LGBTQ and persons with disabilities. In order to obtain comprehensive data, research studies require diverse participants. Representation: Importance of Diversity in Clinical Research StudiesĬlinical studies allow scientists and researchers to answer specific questions about the effectiveness and safety of drugs, vaccines, devices, and treatments. If someone decides they no longer want to participate in the study, they can withdraw at any time. It is a process that continues with ongoing conversations between the research team and participants before, during, and after research participation. Click here to add this to my saved trials. Status: Enrolling, Phase Updated: Dallas Hernia Institute. The process of informed consent does not end when someone signs the informed consent document. Duncanville, Texas 75116 Use our guide to learn which trials are right for you Weve found. Participants should feel comfortable asking questions and discussing with the research team any concerns they might have. It is the responsibility of the research staff to help participants understand the information about the study and give them time to decide if they want to participate. If someone is interested in participating in a study, the research team may provide an informed consent document that includes details about the study, such as its purpose, how long it lasts, required procedures, potential risks, and whom to contact with questions or issues. It is the process of learning the key facts about the clinical study before deciding whether to participate. Informed consent is an essential part of participating in a clinical study.
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