Clin2
NCT07099651Possibly a fitRecruiting

Social understanding in spinocerebellar ataxia

Autosomal Dominant Spinocerebellar Ataxia (SCA1, 2,3,6,7,27B)

Part of Brain & nervous system, Genetic & congenital clinical trials.

This study looks at how people with certain genetic types of spinocerebellar ataxia (a condition that affects movement and coordination) understand social situations. It aims to see if there are differences in social thinking compared to people without the condition.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
160 people
Ages
18 years to 100 years
Study type
Interventional

Who can take part

  • You are 18 years old or older
  • You have completed at least 7 years of school (elementary level)
  • You can read, write, and speak French
  • You are willing to sign a consent form to join the study
  • For patients: You have a confirmed genetic diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7, or 27B
  • For controls: You do not have any known neurological condition

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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