Clinical trial Recruiting at 1 site Interventional Ages 40 to 90

Using brain stimulation to improve symptoms in patients with Multiple System Atrophy - Cerebellar Variant

Official title: Efficacy and Safety of Transcranial dIrect Current stiMulation (tDCS) on Cerebellar Symptoms in Multiple System Atrophy-Cerebellar Variant (MSA-C) (STIM-MSA)

Run by University of Salerno · NCT06821256 · Data updated 2026-11-12

This study is testing if a type of brain stimulation can help improve symptoms and quality of life for people with the cerebellar variant of Multiple System Atrophy.

Quick facts

Study typeInterventional
Ages40 Years to 90 Years
SexAll
Enrollment30 (estimated)
SponsorUniversity of Salerno
Academic / other
Locations1 site (Salerno, Sa)
StatusRecruiting
StartedJuly 3, 2023
Main results expectedDecember 2027
Study endsDecember 2027
Registry record updatedApril 29, 2026
Trial IDNCT06821256 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are individuals diagnosed with Multiple System Atrophy - Cerebellar Variant who can walk independently or with minimal support.

Probably not a fit

Patients with severe sensory deficits, psychiatric disorders, or those with certain medical histories such as seizures or heart problems may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the safety and efficacy of anodal transcranial direct current stimulation (tDCS) in patients with Multiple System Atrophy - Cerebellar Variant (MSA-C). It is designed as a double-blind, randomized, sham-controlled trial with two independent arms, where participants will receive either active or sham stimulation over a period of five consecutive days. The study aims to assess the impact of tDCS on cerebellar symptoms and overall quality of life for patients suffering from this progressive neurodegenerative disease. A total of 30 patients will be recruited, with each participant receiving both types of stimulation in a crossover design.

Why it matters

Potential benefit: If successful, this approach could provide a new non-invasive treatment option to improve symptoms and quality of life for patients with MSA-C.

How similar studies have gone: While the use of tDCS in other atypical parkinsonisms has shown promise, this specific application in MSA-C is relatively novel and untested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Multiple system atrophy cerebellar variant according with the Movemente Disorder Society criteria (Wenning et al 2022)
* Ability to walk either indipendently or with a minimum support

Exclusion Criteria:

* Presence of electrical stimulators (for example, pacemaker, Deep Brain Stimulation, DBS)
* Difficult in understanding Italian language
* Presence of severe sensory deficits (for example, visual or hearing impairments)
* History of drug abuse
* History of severe psychiatric disorders
* History of transient ischemic attacks
* Cortical or sub-cortical vascular lesions
* Seizures or severe heart problems and previous neurosurgical operations
* Pregnancy

Where it's running

  • Centro per le Malattie Neurodegenerative (CEMAND) Dipartimento di Medicina e chirurgia, Sezione Neuroscienze, Università di Salerno
    Salerno, Sa, Italy
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.