Learn about different groups
Including many kinds of people can help researchers see if the possible benefits, risks, or side effects are different across groups.
Including many kinds of people can help researchers see if the possible benefits, risks, or side effects are different across groups.
A broader mix of participants can help trial results better reflect the people living with the condition.
What researchers learn may help guide future studies and the use of a medicine if it is approved.
Some people may not trust medical research because people and communities were harmed or treated unfairly in the past. Other barriers can also make it harder to take part, such as not knowing about clinical trials, travel or time away from work and family, costs linked to taking part, or not having a nearby research site.
Trust must be earned. We work to raise awareness, build local relationships, listen to community needs, and address barriers where possible. If you are considering taking part in a clinical trial, you can visit our Frequently Asked Questions to learn more about safety, what participation involves, and your rights.
Method #1
Designing trials with patients in mind
We design clinical trials to make participation easier and reduce time and effort required from patients. When possible, we also work to include more people by broadening the eligibility criteria.
Method #2
Engaging with local communities
We work with local communities near our clinical trial sites to build trust and share information. This helps more people learn about clinical trial opportunities.
Method #3
Broadening our network of investigators and research sites
We are expanding and diversifying our network of investigators across the country. This helps us reach more communities and improve access to clinical trials.
Investigators and US research sites can use our Site Interest Form to share information about their clinical research experience and capabilities: