FAQs
1. What is a clinical research study?
A clinical research study is a medically supervised project designed to evaluate the safety and effectiveness of new medications, treatments, or medical devices. At ProCare Research Center, all studies follow FDA and Good Clinical Practice (GCP) guidelines to protect participant safety.
3. Do I have to pay to participate
in a study?
There is no cost to participate in our clinical trials. Study-related visits, procedures and tests are typically covered by the study sponsor. In some cases, you may also receive compensation for your time and travel, depending on the specific study.
2. What conditions do you
currently study?
We conduct clinical trials for respiratory and immune-related conditions such as COPD, asthma and psoriatic arthritis. Available studies may change over time, so we encourage you to contact us to learn about our current enrolling trials.
4. Where are you located and what are your office hours?
ProCare Research Center is located at 4822 NW 167th St, Miami Gardens, FL 33014.
Our office hours are:
-
Monday – Friday: 9:00 AM – 5:00 PM
-
Saturday: 9:00 AM – 4:00 PM
5. How do I know if I qualify for a study?
Each study has specific eligibility criteria, such as age, medical history, diagnosis and current medications. Our research team will ask you some questions and may schedule a screening visit to determine if you qualify for a particular study.
​​
​
​
7. Is my information kept confidential?
Yes. Your personal and medical information is protected under HIPAA and other privacy regulations. We follow strict confidentiality policies and only share your information as allowed by law and with your consent, as explained in our Notice of Privacy Practices.
​
​​​
​
​
6. Do I need health insurance
to participate?
Health insurance is not required to participate in most of our clinical research studies. Study-related procedures and visits are typically covered by the study sponsor.
​
​
8. What can I expect during
a clinical trial visit?
During a study visit, you may meet with our research staff and medical investigator, review and sign informed consent forms, answer health-related questions, and undergo exams, lab tests or other procedures required by the study protocol. Our team will explain each step and answer your questions.
​