VOLUNTEER FOR A STUDY
Our work depends on the support of study volunteers. If you or someone you know is looking for free treatment options, along with stipends for your time and participation, joining a clinical trial could be a valuable opportunity. Participating in a trial not only provides access to new treatments but also contributes to advancing medical research for the benefit of all.
Steps from ONE to DONE!
PRE-SCREENING
A phone or clinic conversation to explain the study.
Informed consent
Review and sign a form explaining your rights and duties in the study.
Screening:
Check if you meet study requirements, including vitals, labs, medical history, and exams.
Enrollment & randomization
You are assigned to a treatment or placebo. Neither you nor your doctor will know which one you get.
Study visits
Visits happen days, weeks, or months apart, following the study plan for labs, exams, questionnaires, or other tests.
End of study treatment
Stop treatment and discuss your experience so far.
Follow-up period
Occasional calls or appointments to check on you after treatment.
Completion
Your study participation ends, and you share your final thoughts for improvement.
Clinical Trial FAQs
Clinical Trials
Clinical Trials rely on volunteers to develop and test new medical treatments and devices, demonstrating their safety and effectiveness for FDA approval.
Are clinical trials safe?
Clinical trials undergo close oversight by pharmaceutical companies and the FDA to ensure strict adherence to established guidelines. Throughout the trial and follow-up period, your physician and research coordinator will carefully monitor volunteer health status information to ensure your safety and well-being.
Does it cost anything to participate?
It’s free! You will also be paid for your time, travel, and participation!
Can I participate in a study even if I don’t have insurance?
Insurance is NOT needed. Please refer your coworkers, friends, and family that may be interested in a study too!