Understanding informed consent
What to expect when a study team explains the trial and asks for your consent—in plain language.
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Practical help for navigating clinical trials — from how matching works to what happens with your data.
How it works
Four steps. No waiting rooms, no PDF forms, no phone trees. The whole thing is designed to fit between appointments, not replace them.
Start your intake→A short intake in plain English — your condition, where you live, how far you can travel, and what you'd want a trial to fit around.
Recruiting studies, ranked by how well they actually match. Weak matches are labeled weak. Nothing is dressed up to look better than it is.
Eligibility criteria, visit schedules, and study purpose rewritten so you can understand what you'd actually be signing up for.
Save trials, share them with your clinician, and leave with a short list of questions to bring to the next appointment.
Guides & resources
Clear reading on how trials work, what consent means, and what to ask before you say yes.
What to expect when a study team explains the trial and asks for your consent—in plain language.
Read moreCommon words you'll see in trial listings and consent forms, explained simply.
Read moreQuestions to ask your doctor or a study coordinator, and what to have ready.
Read moreIs it free? Do you store my data? How do I contact a study? Find answers here.
Read moreGet support
Common questions about trials and using the platform.
Trust foundation
What we keep, what we don’t, and how the data you share is handled — so you can focus on finding options.
For full details on data handling, retention, and your rights.
Read our Privacy PolicyNewsletter
Tips on finding trials, preparing for the next conversation, and the occasional product note. No spam.
Keep going
Look at the platform, read about what we’re building, or send us a note.