Too often, health care is one-size-fits-all. But imagine a future where prevention, treatment, and care are tailored for YOU.
That future starts with research that includes all of us.Learn more
Part of the National Institutes of Health, All of Us is changing how health research is done.
We're building one of the largest and most diverse health databases of its kind.
Researchers are already using this data to learn more about why people get sick or stay healthy, and what makes each of us unique.
They're using this information to find better ways to prevent and treat illnesses and to care for all of us.
But there's more to do.Learn more
Many groups have been left out of health research in the past. You can help change that.
Researchers need information from large numbers of people who reflect the diversity of the United States. Our goal is to reach more than 1 million people from all backgrounds.
If you join All of Us, we will ask you to answer health surveys and connect your electronic health records and wearable devices. We may also ask you to share biosamples (like blood, urine, and saliva).
All of this information helps paint a full picture of what makes each of us unique. It helps researchers understand how our health history, genetics, environment, and life experiences impact our health.
I joined the All of Us Research Program because I believe that health care should be as unique as each one of us and I want to be part of it.Hugo (he/him)
Medical research has not always focused on minorities or Latinos. I think it's important for my generation to share our health information to help future generations.Carlos (he/him)
I signed up for the All of Us Research Program because I represent a group that has historically been underrepresented in research and I want to be counted.Keisha (she/her)
I believe firmly that the All of Us Research Program will be the first step in generating new discoveries that will translate into patient care.Dr. Jason Karnes (he/him) uses genomic data to learn about adverse drug reactions
All of Us is a research program and does not provide health care or medical advice.Sign up today
All of Us follows all laws and rules for keeping the data you share with us safe and private.
We often test the security of our databases. Before making data available to researchers, we remove personal details that could identify you. We also require researchers to go through training. They must agree to our data use rules.Learn more about privacy
All of Us requires training to make sure that every researcher who wants to use the Workbench understands how to really follow the rules set in place by All of Us.
The safety, the security, and the ethics of this program are at the highest level. We really care about our participants as partners.
It’s an easy thing to do, it’s safe, it’s secure, and I hope you’ll be involved too.
They do a great job of protecting people who may disclose things through the All of Us data set ... that may not necessarily be disclosed in their day-to-day lives.
Learn more from the Voices of All of Us
So far, more than 765,000 people have joined the program. More than 80% of All of Us participants are from groups that have rarely been part of health research.
*Fully enrolled participants are those who have shared their health information with All of Us, including giving blood and urine or saliva samples.
Last updated: February 20, 2024Sign up today
All of Us works closely with Health Care Provider Organizations around the country to make joining easy.
People who live too far from a partner site can join online.