Clinical Research Studies FAQ in Tampa, FL
Got Questions? Read below and discover some information and resources that are useful for you as to whether or not you want to participate in Clinical Research Studies in Tampa, Florida.
Clinical research is conducted with a direct interaction to human volunteer. Clinical research helps doctors and researchers find new and better ways to understand, detect, control, and treat illness.
A protocol describes what type of people are eligible to participate in the study; determines the schedule of tests, procedures, medications, and dosages; and sets the length of the study.
A clinical trial is a research study in which one or more human volunteers are prospectively assigned to one or more interventions to evaluate the effects of those interventions on health-related biomedical or behavioral outcomes.
Every clinical trial has specific criteria related to the type of participants that are needed for the study. These criteria exist to ensure that good statistical data can be collected for the study to achieve its purpose. Additionally, in order to ensure that no undue risk or coercion is placed upon study volunteers, certain populations are considered special populations that must receive a higher degree of safety and ethical oversight. These populations include children/minors, pregnant women, indigents, prisoners, and other vulnerable populations.
The very first thing that will happen if you choose to volunteer for a clinical trial is you will be provided a full explanation of the study, including required tests and procedures, visits that you have to attend, as well as potential risks and benefits of the study. If you agree to participate in the study, you will always be able to stop participating at any time. While in the study, you will only be asked to complete the visits and procedures that were specified in the beginning. The goal of the study is to collect valuable data from you that will help the researchers during the study.
Without clinical trials, all of the medications and treatments that we have today would not exist. In order to develop new treatments that are both safe and effective, testing must be done. The Food and Drug Administration (FDA) requires that all medical treatments or methods be vigorously tested to ensure that they are both effective and generally safe. Volunteers of clinical trials provide a valuable service to the community to help researchers advance medical science and improve healthcare for generations to come.
Source for FAQs: National Human Genome Research Institute