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On July 10, 2026, this site will be winding down to focus on delivering a more streamlined, modern experience across other platforms. See below.
The MnTiC Registry connects you to our research opportunities online and/or in-person. By joining the registry, you will be contacted when there's a study for which you might be eligible. People from most countries around the world are eligible to join. Participants who are under 18 will need a parent or guardian to sign them up.
The MnTiC Registry aims to increase access through online participation and help more people get better treatment faster improving the way tics are diagnosed. You are eligible to join if you are 18 or above (or your parent or guardian signs you up), read English, and experience tics. People from most countries around the world are eligible to join!
Goals
Improve our understanding of tics in a way that helps the tic community.
Create opportunities for people with tics to participate in research online and in-person.
Make it easier to reach people affected by tics, regardless of where they live, for research and treatment.
Help scientists learn how to better diagnose and treat tics.
Collect data from a larger number of people, which could help us speed up scientific research and discoveries about tic disorders.
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