Spinocerebellar ataxia type 29
MONDO:0007298Spinocerebellar ataxia type 29 (SCA29) is a rare subtype of autosomal dominant cerebellar ataxia type I (ADCA type I) characterized by very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability.
Also known as: SCA29, congenital nonprogressive spinocerebellar ataxia, spinocerebellar ataxia 29, congenital nonprogressive, spinocerebellar ataxia type 29, ACV, aplasia of cerebellar vermis, cerebellar ataxia early-onset nonprogressive, cerebellar ataxia, congenital nonprogressive, autosomal dominant
20 clinical trials for this condition and its sub-types, 1 tagged with Spinocerebellar ataxia type 29 itself.
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Robots as rehab coaches: a new approach to retraining coordination in ataxia
Disease control OngoingThis trial tests whether robot-assisted neurorehabilitation can improve coordination, balance, and walking in adults with ataxia, a condition that affects movement control. Participants will receive either robotic or standard rehabilitation, and researchers will measure changes i…
Sponsor: Somogy Megyei Kaposi Mór Teaching Hospital • Aim: Disease control
Last updated Jul 31, 2026 00:00 UTC
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Can a gentle brain zap help people with ataxia walk better?
Symptom relief OngoingThis study tests whether a non-invasive brain stimulation technique called transcranial direct current stimulation (tDCS) can improve movement in people with degenerative ataxia, a rare condition that damages the cerebellum and impairs balance and coordination. Sixteen participan…
Sponsor: University of Cagliari • Aim: Symptom relief
Last updated Jun 27, 2026 08:00 UTC