Clinical Research
Education Hub

Learn valuable information about clinical studies — from how they work to ways to get involved.

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Real People.
Real Experiences.

Hear from individuals who participated in clinical studies and learn how it made a difference in their lives.

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I’m not a doctor, but I can tell people about my experiences. I can encourage other patients to ask questions and research on their own, and I try to teach them how to be an advocate for themselves. 

Patient Story

The Road To New Treatments

Clinical studies help turn today's research into tomorrow's treatments.

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01

Find a
Clinical Study

02

Contact the
Research Team

03

Share Your
Medical Records

04

Sign Consent
& Participate

How do I Participate in a Clinical Study?

There are several resources you can use to find a clinical study that's best for you.

Contact PatientWing

Talk with your physician

  • They can offer advice and help determine if a clinical study is suitable for you.
  • Use our Physician Discussion Guide during your conversation.

Local hospitals or universities

Many organizations conduct their own studies and may have listings on their websites. Search for "Clinical Trials" or use the "Contact Us" form on their website to request information.

ClinicalTrials.gov
A comprehensive database of publicly and privately funded clinical studies.

To determine if you are a good fit for the study, the research team needs to review your medical records.

Use our Medical Records Guide to learn how to send your medical records to a research site.

Reach out to the study's contact person for more information. They can answer your questions about the study, review the number of visits, and share any potential risks.

If you're working with PatientWing, we will connect you directly to the research team!

If you decide to participate, you'll need to sign a consent form to begin the screening process. If you're eligible for the study, attend all scheduled visits and follow the study's instructions while participating.

Read more about What to Expect During Clinical Study Participation.

Find your Study

Explore clinical studies that are currently enrolling.

Learn About your Condition

Explore all conditions

Benefits of Clinical Research

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Access to investigational treatments

Support from research teams

Study-related health monitoring

Connection and community

Study-related care at no cost*

Help advance future treatments

*Benefits and costs vary by study. The study team will explain what applies.

Meet The Experts

Get to know the investigators conducting clinical studies.

View all investigator profiles
Dr. Emily Chen, MD, PhD

Gary W. Falk, MD, MS

Director of the Esophagology and Swallowing Center in the Gastroenterology Department

View Profile

More Topics

Learn more about clinical research through our educational resources,guides and helpful information.

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Frequently Asked Questions

What is a clinical study?

A clinical study tests new treatments to see if they are safe and effective for people. Researchers study the effects of new drugs, medical devices, or treatments in a controlled environment to gather data on their benefits and risks.

How do I know if I am eligible for a study?

Eligibility is determined by specific criteria related to your condition, age, medical history, and other factors. The research team will review your information to see if you meet the study criteria.

Can I leave the study if I change my mind?

Yes! You can withdraw from the study at any time without consequence. However, it’s important to inform the research team so they can ensure you leave the study safely.

Are there any costs associated with participating in a clinical study?

Most studies are available at no cost to you! You likely do not need to pay for treatments related to study care and many studies do not require insurance. Many studies cover travel costs too. However, you may need to pay for travel and discuss reimbursement options with the research team.

How will the study results be used?

The results will be analyzed to determine the effectiveness and safety of the new treatment or procedure. Findings may be published in medical journals or presented at conferences, and they contribute to advancing medical knowledge and potential treatment options.

What will happen during the study?

The study may involve a series of visits, tests, and possible treatments according to the study protocol. The research team will explain each step in detail, including any procedures and time commitments required.

Will I be compensated for my participation?

Some studies offer compensation for your time and travel expenses. Compensation details will be provided by the research team.

How is my privacy protected during the study?

Your personal information and medical records will be kept confidential and secure. The research team will follow strict guidelines to protect your privacy and ensure that your data is used only for the study’s purposes.

What if I experience side effects or health issues during the study?

Report any side effects or health issues to the research team immediately. They will monitor your health throughout the duration of the study and provide appropriate care. Your safety is a top priority, and they will take steps to address any concerns.

Who will oversee my care during the study?

A team of healthcare professionals, including doctors and nurses, will oversee your care during the study. They are trained to manage your health and ensure that the study is conducted safely. You should always speak with your doctor prior to beginning a clinical study. Click here to read and download the Patient and Physician Discussion Guide.

How is the study regulated to ensure it is safe?

Clinical studies are regulated by government agencies, such as the Food and Drug Administration (FDA) in the United States, and must follow strict ethical and safety guidelines.

Will the study impact my current treatment?

Some studies may require you to stop or adjust your current treatment, while others allow you to continue your current treatments. Before you make any changes to your medications, you should speak with the research team and your doctor.