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Transcranial Alternating Current Stimulation (tACS) in Patients With Ataxia

Not Applicable
Completed
Conditions
Ataxia
Ataxia With Oculomotor Apraxia
Multiple System Atrophy
Spinocerebellar Ataxias
CANVAS
Interventions
Device: Transcranial stimulation over the cerebellar hemispheres
Registration Number
NCT05621200
Lead Sponsor
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
Brief Summary

The aim of the study is to evaluate the effects on motor and cognitive performance of transcranial alternating current stimulation (tACS) compared to transcranial direct current stimulation (tDCS) and placebo stimulation (sham) in patients with neurodegenerative ataxia to identify a possible rehabilitation protocol.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
26
Inclusion Criteria
  • Patients with a cerebellar syndrome and quantifiable cerebellar atrophy
Exclusion Criteria
  • Severe head trauma in the past
  • History of seizures
  • History of ischemic stroke or hemorrhage
  • Pacemaker
  • Metal implants in the head/neck region
  • Severe comorbidity
  • Intake of illegal drugs
  • Pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Transcranial direct current stimulation (tDCS)Transcranial stimulation over the cerebellar hemispheresSingle session of anodal tDCS at 2 mA over the cerebellar hemispheres
Transcranial alternate current stimulation (tDCS)Transcranial stimulation over the cerebellar hemispheresSingle session of gamma tACS (50 Hz) at 3 mA over the cerebellar hemispheres
Placebo stimulation (sham)Transcranial stimulation over the cerebellar hemispheresSingle session of sham tDCS over the cerebellar hemispheres
Primary Outcome Measures
NameTimeMethod
Change in the International Cooperative Ataxia Rating Scale (ICARS) Score From BaselineBaseline (immediately before the intervention) - Immediately after the intervention

International Cooperative Ataxia Rating Scale (ICARS): semi-quantitative 100-point scale, yielding a total score of 0 (no ataxia) to 100 (most severe ataxia).

Change in the Scale for the Assessment and Rating of Ataxia (SARA) Score From BaselineBaseline (immediately before the intervention) - Immediately after the intervention

Scale for the Assessment and Rating of Ataxia (SARA): 8-item performance based scale, yielding a total score of 0 (no ataxia) to 40 (most severe ataxia).

Secondary Outcome Measures
NameTimeMethod
Change in Walking Cadence From BaselineBaseline (immediately before the intervention) - Immediately after the intervention

Average Left and Right Steps/Minute during a 60 seconds walk, assessed with gait sensors.

Change in 360° Turn From BaselineBaseline (immediately before the intervention) - Immediately after the intervention

Velocity (Number of Degrees/sec) in making a 360° turn, assessed with gait sensors

Change in Timed Up and Go Test Duration From BaselineBaseline (immediately before the intervention) - Immediately after the intervention

Time (in seconds) that a person takes to rise from a chair, walk three meters, turn around 180 degrees, walk back to the chair, and sit down while turning 180 degrees, assessed with gait sensors.

Change in Cerebellar Brain Inhibition (CBI) Measurements From BaselineBaseline (immediately before the intervention) - Immediately after the intervention

Cerebellar brain inhibition (CBI) is expressed as motor evoked potential amplitude (average of 10 recordings). Lower values reflect higher inhibition and thus reduced impairment.

Trial Locations

Locations (1)

ASST Spedali Civili di Brescia

🇮🇹

Brescia, BS, Italy

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