Your Rights as a Research Participant
At Apollo Pact, we believe that people who step forward to participate in clinical research—especially psychedelic studies—deserve more than just protection. They deserve to be seen, heard, and respected as partners in the future of medicine.

As a research participant, you have the following rights:

You Have the Right To...

1. Be Treated with Respect and Dignity
Your voice matters. You have the right to be treated as a whole person—not a subject, not a case, but a human being with agency, values, and lived experience.

2. Understand What You’re Agreeing To
Before joining a study, you have the right to receive clear, honest information about what the research involves—including why it's being done, what you'll be asked to do, and what risks and benefits may be involved.

3. Make a Free and Informed Choice
You have the right to say “yes” or “no” to participating—without pressure, judgment, or fear of losing access to care. And you can change your mind at any time.

4. Ask Questions and Get Real Answers
You deserve transparency. Ask anything—at any time. The research team should give you answers you understand and feel comfortable with.

5. Know Your Options
You have the right to learn about other available treatments or choices outside the study. No one should ever make you feel like this is your only path.

6. Have Your Privacy Respected
Your personal and health information must be kept confidential. You have the right to know who will see your data and how it will be used.

7. Receive a Copy of What You Sign
You have the right to a copy of the consent form and any materials you agree to. You should always know what you’ve signed and why.

8. Withdraw Without Consequence
You can stop participating in a study at any time, for any reason. You don’t need to explain—and it won’t affect your access to care or support.

9. Report Concerns Without Fear
If something doesn’t feel right, you have the right to speak up. Whether it’s a safety issue, communication problem, or ethical concern, your voice is protected.

10. Be Part of the Bigger Picture
You have the right to know how your participation contributes to broader understanding. You’re not just helping science—you’re helping future patients, families, and communities.

At Apollo Pact, we were founded by people who have walked this path—as participants, as advocates, and as believers in the power of ethical research. We're here to ensure that your experience in clinical research is guided by trust, transparency, and compassion.

If you have questions, concerns, or want help navigating a clinical trial, we’re here for you.

Contact us at hello@apollopact.org

We believe research should serve people—not the other way around.