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Stanford University School of Medicine

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Stanford University School of Medicine logo

PRIDEnet at Stanford University School of Medicine has partnered with the All of Us Research Program.

Watch the All of Us Anthem Video Image of a young man with a link to All of Us video Play

For years, Stanford University School of Medicine has worked to increase awareness about and participation in clinical and biomedical research within vulnerable populations, including the LGBTQ community. We work to ensure that the All of Us Research Program has access to information about how to engage and support our communities. And, together with the National Institutes of Health (NIH), we are calling on the LGBTQ community to help make history and change the future of health.

The health data you share will be added to the All of Us Research Program database. Researchers can access this data to conduct studies. This could help them see how different things, like environment, lifestyle, and genes, can impact health. This may help develop new medical treatments that are unique to each person.
 

LEARN MORE ABOUT THE PROGRAM

How to Join

You can sign up using this website or call to make an appointment. If you do not finish signing up online, you can continue the process in-person; whichever is most convenient for you.

Get in Touch

Please contact us to learn more about participating in the program.

Stanford University School of Medicine (415) 408-5995
Image of Robert Winn
“Most studies and most clinical trials have always been with the average white male. So as we start thinking about this, in the context of building trust, I think we get back that trust by involving the community.”
Robert Winn, MD Director of Cancer Center
Associate Vice Chancellor, Community Based Practice University of Illinois
Frequently Asked Questions
What will you do to protect my privacy?

Your privacy is very important, and we will take great care to protect it if you join. Here are a few of the steps we will take:

  • Information we collect will be stored on protected computers. We will limit and keep track of who sees the information.
  • We will remove your name and other direct identifiers (like your Social Security number) from your information and replace them with a code. There is a master list linking codes to names. This list is kept secure, and very few people have access to it.
  • To work with your health information, researchers must promise not to try to find out who you are.
  • We will tell you if there is a data breach.
  • The All of Us Research Program has Certificates of Confidentiality from the U.S. government. This will help us fight legal demands (such as a court order) to give out information that could identify you.

Still, loss of privacy is a risk of taking part in the All of Us Research Program. Even without your name, there is a chance someone could figure out who you are. Your information could be misused. We believe the chance of this is very small, but it is not zero.

What will you ask me to do?

If you decide to join All of Us, we will ask you to share different kinds of information. We will ask you basic information like your name and where you live. We will ask you questions about your health, family, home, and work. If you have an electronic health record, we may ask for access. We may ask you to go to a local clinic or drug store for a free appointment with us. At this appointment we would measure your weight, height, hips, and waist, as well as your blood pressure and heart rate. We might ask you to give samples, like blood or urine, at the appointment. We also want to know if you will want information about your DNA.

Why should I join the All of Us Research Program?

If you join, you will be contributing to research that may improve health for everyone and for future generations. Our goal is to understand how different factors together affect health and speed up research to develop new and tailored treatments. Here are some examples of what researchers might be able to discover from their research:

  • Better tests to see if people are sick or are at risk of getting sick.
  • Better mobile apps to encourage healthy habits.
  • Better information about which or how much of a medicine is right for each person.

Also, you will be able to see your All of Us information, which might be interesting to you. It may help you learn about your health. Adult participants may also learn about their DNA, if they choose to. Participants can share any information they receive from All of Us with their doctor, if they choose.

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Our FAQ library has the answers to over 60 common questions.

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