Have you ever wondered about the development of medications or medical treatments that could one day improve the health and quality of life of millions of people?
Clinical trials are a fundamental part of this process. Volunteer participation in paid clinical trials is essential for the development and approval of new medications and medical treatments.
To come up with newer, better treatment methods and medications, pharmaceutical companies must conduct research and clinical trials. These trials help them to learn how a medication works, who might benefit from it, how safe it is, and how effective it is.
That is where Research Centers of America (RCA) comes in. As one of Broward County’s leading clinical research companies, RCA’s areas of expertise include general medicine, mental health, and substance abuse, so we have conducted an incredibly wide range of clinical studies over the years. Our knowledgeable research professionals have looked at everything from Alzheimer’s and fibromyalgia to anxiety and autism.
We work with volunteers who suffer from the conditions in question to learn how they are affected by in-progress treatments and medications, so they can be altered and improved before hopefully moving on to wider medical use.
Clinical studies are a necessary and incredibly valuable part of the process, and the people who volunteer to participate in them may benefit not only themselves but also countless others in the future. If you or someone you love is battling addiction, a medical condition, or mental illness, you may be able to join one of our studies at RCA.
What is a Clinical Trial?
A clinical trial is a research study in human volunteers intended to answer particular health questions. Clinical trials at South Florida Clinical Research are conducted to develop new medications or treatments that can improve health. After a medication or treatment is found to be safe and effective, it may be approved by the FDA and then, it will be available for population.
No treatment may reach clinical testing unless there is evidence that there might be an improvement over current therapies.
Why Participate in a Clinical Trial?
Medical treatment cannot improve without research and volunteers. Everyone would like a successful treatment available when diagnosed with an illness. By volunteering for clinical trials in Miami you can help advance knowledge about future treatments that someday you and a loved one may benefit from.
In a research study in clinical trials in Miami you have the ability to take an active role in your own health, access possible investigational medications/treatments before they are widely available, and help others by contributing to the participants in return for their time and travel.
Who Can Participate in a Clinical Trial?
All clinical trials in South Florida and elsewhere have guidelines about who can get into a specific study. The factors that permit someone to participate in a clinical trial are called “inclusion criteria” and those that forbid someone from participating are called “exclusion criteria”.
These criteria are based on such factors as age, gender, the type and stage of a disease, previous treatment history, and other medical conditions. In order to join clinical trials Miami, a participant must meet the requirements for the study. Some research studies seek participants with illnesses or conditions to be studied in the clinical trial, while others need healthy participants. Inclusion and exclusion criteria are used to identify proper participants and keep them safe. The criteria help ensure that research questions will be answered properly.
Learn More About Clinical Trials
What Happens During a Clinical Trial?
The clinical trial process depends on the kind of trial being conducted. The clinical trial team, whether conducted at medical clinics in Miami or elsewhere, includes doctors, nurses and other health care professionals. These professionals will check your health at the beginning of the trial, give you specific instructions for participating in the trial, monitor you carefully during the trial, and stay in touch after the trial is completed.
Some clinical trials Miami include more tests and doctor visits than you would normally have for an illness or condition. Your participation Miami clinical trials will be more successful if you follow the protocol carefully and stay in contact with research staff.
What is Informed Consent?
Informed consent is the process of learning the key facts such as its purpose, duration, required procedures, and key contacts about a clinical trial, before deciding whether or not to participate. When you decide to join a clinical trial you will receive an informed consent document that includes the details about the Study. You can always ask for the consent documents in different languages other than English. Joying a clinical trial is a very important decision so, you must ask the research team any questions you may have about the study and the consent forms before you make a decision.
What Are the Benefits of Participating in a Trial?
Besides playing an active role in your own health care and helping others by contributing to medical research, by participating in South Florida clinical trials you can also enjoy benefits like:
- Have access to new medical treatments or medications that are not available in the market or in medical clinics in Miami.
- Obtain medical care at top health care facilities during the trial.
- If you qualify you may receive a stipend to help compensate for time and travel.
How is the Safety of the Participant Protected?
The ethical and legal codes that govern medical practice also apply to Miami clinical trials and most of the Miami clinical trials are federally regulated with built in safeguards to protect the participants. The trial, including each South Florida clinical trial, follows a carefully controlled protocol, a study plan which details what researchers will do in the study. As a clinical trial progresses, researchers report the results of the trial at scientific meetings, to medical journals, and to various government agencies. Individual participants’ names will remain secret and will not be mentioned in these reports.