For participants
Help Shape the Future of Medicine
Clinical trials give participants the opportunity to contribute to medical progress while receiving support from a dedicated research team.
The basics
What is a clinical trial?
A clinical trial is a carefully designed research study that helps doctors and scientists learn whether a new treatment, medication, or approach is safe and effective.
Trials follow a detailed plan called a protocol, and every step is reviewed for safety. People take part for many reasons, and participation is always voluntary.
Informed consent
You will never be asked to decide without information
Before joining a study, you will have the opportunity to ask questions and review the informed consent form. This document explains the purpose of the study, what will happen during visits, possible risks and benefits, privacy protections, and your rights as a participant.
Joining a study is always your choice. You can take time to review the information, talk with family or your doctor, and decide whether participation feels right for you.
Oversight
Who reviews clinical trials?
Clinical trials are reviewed by an Institutional Review Board, also called an IRB. The IRB helps protect participants by reviewing the study before it begins and making sure participant rights, safety, and privacy are considered.
Why participate?
Reasons people take part
Taking part in a study does not guarantee a medical benefit. Your research team will explain what to expect for each study.
What to expect
Your journey, step by step
Find a study that fits you
Browse trials enrolling now near you.
Complete a quick, secure online pre-screening
A few minutes to see if you may qualify.
Speak with the research team
Ask questions and learn more about the study.
Review informed consent
Understand the study fully before you decide.
Attend scheduled study visits
Care and monitoring throughout the study.
Receive follow-up and support
Ongoing support from the research team.
After you apply
What happens after I apply?
After you complete a pre-screening form, a member of the Wellness Clinical Research team may contact you to ask additional questions and explain the study in more detail. Completing a form does not mean you are enrolled. It simply helps the research team determine whether the study may be a possible fit.
You complete a secure pre-screening form
Our team reviews your answers
We contact you if the study may be a fit
We answer your questions
If appropriate, we schedule a screening visit
You review informed consent before deciding
Your safety comes first
Protected, informed, and always in control
Informed consent means you'll understand the study before you decide. Your privacy is protected, and studies are overseen by an ethics board (IRB).
You may withdraw at any time, for any reason, without affecting your regular medical care.
Common questions
Frequently asked
Is participation free?
There is typically no cost to you for study-related care. Some studies offer compensation for time and travel, your research team will explain the details for each study.
Can I leave a study after I start?
Yes. Participation is always voluntary, and you can withdraw at any time, for any reason, without affecting your regular medical care.
Will my information be kept private?
Yes. Your privacy is protected, and your information is handled according to applicable regulations and the study protocol.
Does pre-screening mean I'm enrolled?
No. Pre-screening helps the team see if a study may be a fit. A member of the research team will review your information and contact you to discuss next steps.
Will my regular doctor be replaced?
No. Clinical trial participation does not replace your regular medical care. You should continue seeing your regular healthcare providers unless the study team explains otherwise.
What if I do not qualify?
Not qualifying for one study is common. You may still be considered for future studies that better match your health history or interests.
Is my information private?
Your information is handled according to privacy and research requirements. The study team will explain how your information may be used and protected before you decide to participate.