Below are some of the most common questions that we receive daily. In addition, we highly encourage you to ask our recruitment coordinators the following questions:
- How much time does it involve?
- How long is each visit?
- Why am I being contacted for this study?
- How long is this study?
- What if I change my mind after joining your study?
- Can I get compensated for participating?
Our study team is available to answer your questions and provide the information that you need. You can email or call our numbers.
Frequently Asked Questions:
Q: Why participate in Clinical Trials?
A: Participants take part in clinical trials for different reasons. To us, they are considered heroes. Some with an illness or disease also participate to help others and to receive the newest treatment. Clinical trials offer hope for many participants and an opportunity to help researchers and the medical community find better treatments for others in the future.
Q: Do you accept walk-in appointments?
A: Typically no, we only accept appointments. Contact us via email or call one of our offices to schedule an appointment. We’re open 6 days a week for your convenience.
Q: Do I need Medicare or medical insurance to join your study?
A: No cost to participate in the clinical trials. Some of the benefits are: medical exams, comprehensive blood tests, study-related medications, and compensation for study-related time and travel.
Q: How do I know if I am qualified to participate?
A: Clinical trials operate under a protocol, a comprehensive set of guidelines specific to each study. Some trials are tailored for individuals with particular medical conditions, while others focus on healthy volunteers. The protocol defines criteria for participation, including who can or cannot join, based on factors like medical history and current health. This ensures that each study enrolls the most qualified participants.
Q: What does participate in a trial/study involve? How much time does it need?
A: Great question! Most of our trials take place in outpatient clinics, similar to your regular doctor’s office. Study visits typically include routine check-ups, physical exams, vitals, EKGs, comprehensive blood panels, and urine samples. Additionally, participants are often required to complete daily electronic diaries as part of the study.
Q: Can I discuss this with my family and my physician before participating?
A: The potential risks and benefits are outlined in the informed consent form. We encourage you to speak with your family and your physician before participating. Since it may require time and dedication to participate. We truly appreciate your time and effort to learn more about our trials and processes.
