Below, you’ll find our comprehensive clinical trial FAQs covering safety, compensation, eligibility requirements, and what to expect before, during, and after a study.
What is a Clinical Trial?
A clinical trial is a research study that evaluates new medications, devices, or treatment approaches to determine if they are safe and effective. Clinical trials help doctors and researchers develop better treatments for current and future patients. All studies follow strict safety guidelines and are carefully monitored.
Why Should I Join a Clinical Trial?
Participating in a clinical study is a great way to help with the development of new and improved medications. As a study participant, you may also be eligible to earn compensation or reimbursement for your time and participation.
Who Can Participate in a Clinical Trial?
Each clinical study has specific requirements for participants based on factors such as age, medical history, and current health status. The eligibility criteria in each study protocol are used to identify the volunteers best qualified to participate.
Is It Safe to Participate in a Clinical Trial?
Participant safety is our top priority. Clinical trials are reviewed and approved by an Independent Review Board (IRB) and monitored by regulatory agencies like the FDA. You will be closely monitored by qualified medical professionals throughout the study, and your health always comes first.
Will I Receive a Placebo?
Some studies include a placebo (a substance with no active medication) for comparison purposes. If a study includes a placebo, this will be clearly explained to you during the informed consent process before you decide whether to participate.
Is There Any Cost to Participate in a Clinical Trial?
No. Study-related medications, lab tests, and medical visits are provided at no cost to you. Participating in a clinical trial should never require you to pay for study-related care.
Will I Be Paid for Participating?
Many studies provide compensation for your time and travel. Compensation amounts vary by study and will be fully explained before you decide to enroll.
Do I Need Medical Insurance to Join a Clinical Trial?
Health insurance is not required for most clinical trials. All study-related care, procedures, and doctor visits are typically provided at no cost to you.
Can I Continue Seeing My Regular Doctor While in a Trial?
Yes. Participating in a clinical trial does not replace your primary care physician. In many cases, your regular doctor can continue managing your general health while our study team oversees your study-related care.
Can I Drop Out of the Study at Any Time?
Participation is completely voluntary. You may choose to leave a clinical trial at any time, for any reason. Your decision will not affect your regular medical care or relationship with your doctor.
How Long Does Participation Last?
Each study is different. Some studies last a few weeks, while others continue for several months or longer. The expected time commitment will be clearly explained before you enroll.
How Do I Know If I Qualify to Participate in a Clinical Trial?
Each study has specific eligibility criteria. The best way to find out if you qualify is to complete our online eligibility form or speak directly with a member of our research team.
How Is My Personal Information Protected?
Your privacy is extremely important to us. All clinical trials follow strict confidentiality and HIPAA guidelines to protect your personal health information. Your data is handled securely and shared only as required for research purposes.
What Is an 'Informed Consent' Document?
Informed Consent is a formal process that explains all the details of the study, including potential risks, benefits, and your rights as a participant. You will receive all the facts about the study—including potential side effects of the investigational product—to help you decide if you want to participate.
What Happens After I Submit an Application Form?
Once you submit a form, you will be contacted by a volunteer recruiter from the Eximia Research team. The recruiter will discuss available studies and ask a few pre-screening questions to confirm your eligibility. If you qualify, the next step is to schedule an in-person screening appointment.
What Happens at the First Screening Visit for a Clinical Trial?
At your first screening visit, you will receive detailed information about the study and can decide if you wish to participate. The study team may perform tests such as vital signs, a physical exam, blood work, and questionnaires. If your results match all study requirements, you will be given the option to enroll.
How Do I Find a Clinical Trial Near Me?
Finding open research studies in your area is easy! You can browse active studies by location or health condition directly through our Find a Study search page.