For Research Champions

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Diversity matters in clinical trials.
Diversity is critical in research to ensure health care and outcomes are ethical and equitable. Research helps us better understand health disparities.
Researchers working
Racial and ethnic minority populations are underrepresented in clinical trials.
According to the Food & Drug Administration (FDA), in 2020, 75% of trial participants were white, 11% were Hispanic, 8% were Black, and 6% were Asian.
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Your health matters.
Minority participation in clinical trials is critical for the development and understanding of new therapies, and to create equality and eliminate disparities in the field.
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Help make a difference in the health of your community.
Participation in clinical trials allows participants to play an active role in their own health, contribute to the advancement of medical knowledge, and make a positive impact on the health of your community.

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Learn more about our frequently asked questions here. 

We respect your privacy.

UI Health Research Registry is a secure, password-protected database. All the information that you choose to share will be kept private and confidential.

Read Our Notice of Privacy Practices & Cookie Settings.

We do nothing without your consent.

UI Health Research Registry is a free and secure tool that facilitates a partnership between health researchers and volunteers. Your membership lets us know that you may be interested in participating in clinical studies, but you are never obligated; you are always free to say no, and can specify how often you would like to be contacted. You can deactivate your account at any time.

Read Our User Agreement Document.

We’re here to help!

If you have any questions or concerns about how your personal data is used, please contact us at healthresearch@uic.edu.

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Learn how you can get involved in research today.

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