Registry Study for Adults with Tic Disorders Comparing Tic Severity and Impact in Women and Men

What this Trial Is About

This research aims to develop a registry for adults with tic disorders to better understand how tic severity relates to the impact on daily life, particularly comparing women and men with these conditions. The study is observational, focusing on collecting detailed information rather than testing specific treatments. Participants will complete various quality of life and symptom questionnaires, including scales like PUTS, OCI, TS-QOL, ASRS, GAD-7, PHQ9, and TAPS. These assessments help to capture the severity of tics and their effects. The main focus is on gathering data to analyze the relationship between tic severity and quality of life over a six-month period. During the study, participants will be asked to fill out these questionnaires, which provide insight into their symptoms and well-being. Researchers will measure the correlation between quality of life and tic severity at six months, as well as any changes in tics during this time. The study involves ongoing observation without treatment intervention, and participants involvement will last at least six months to allow for these assessments.

Adult Tic Disorders Registry