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Understanding and manipulating neural compensatory mechanisms in SCA3 patients

Understanding and manipulating neural compensatory mechanisms in SCA3 patients - Compensatory mechanisms in SCA3

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38791
Enrollment
40
Registered
2013-07-25
Start date
2014-01-24
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebellar ataxia coordination difficulties

Interventions

None listed

Sponsors

Radboud Universiteit Nijmegen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Proven mutation of the SCA3 gene Age > 18 years Symtomatic ataxia SARA score of gait is maximally 3 (they need to be ambulant)

Exclusion criteria

Exclusion criteria: Contraindications for MRI scanning (e.g. pacemaker, claustrofobic) Epilepsy Other neurological disorders Other gait disorders

Design outcomes

Primary

MeasureTime frame
- Changes in grey matter volume (cerebellum or other brain areas) -Changes in functional connectivity between the cerebellum and the rest of the brain -Changes in the neural circuitry that supports gait and balance We will focus on changes between patients and controls, as well as between patients before and after training

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)