Under construction – not a live service
Sign in
Taking people in United StatesNo phase

Brain stimulation combined with rehabilitation therapy for cerebellar damage

Tests gentle brain stimulation alongside rehabilitation in adults with cerebellar damage.

Plain-language title generated from the registry record
Registry title: Individualized Neuro-Modulation Paired With Cerebellar Therapy

Key facts

Where
Baltimore, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT07642856, who can take part

Where in United States

  • Motion Analysis Lab in the Kennedy Krieger InstituteBaltimore, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
Trial code
NCT07642856
Record updated
11 June 2026
Original description
The purpose of this project is to evaluate feasibility and preliminary efficacy of pairing personalized transcranial direct current stimulation (tDCS) with individualized rehabilitation therapy in people with cerebellar damage.Read full original descriptionShow less

Individualized Neuro-Modulation Paired With Cerebellar Therapy

The purpose of this project is to evaluate feasibility and preliminary efficacy of pairing personalized transcranial direct current stimulation (tDCS) with individualized rehabilitation therapy in people with cerebellar damage.

Inclusion: Age 18-75 years; Males and Females; Disorders that predominantly affect the cerebellum: damage from stroke, tumor or degeneration (genetic or non-genetic causes, congenital hypoplasia).

Exclusion: Specific medications: tricyclic anti-depressants or neuroleptic medication; Heart pacemaker or other MRI-incompatible implanted metal device; Seizures or history of seizure disorder; Alcohol or substance use disorder (self-report); Diagnosed history of severe psychiatric disorder such as depression, schizophrenia (self-report); Any medical condition (including orthopedic, pain, cardiopulmonary or other) that limits safe participation in exercise training; Diagnoses or impairments that interfere with task execution or data interpretation; Metallic foreign body in their eye or head; Experience with severe claustrophobia; Experience discomfort from the MRI scan, such as excessive heating of tattoos; Metallic foreign body in their eye or head (except the mouth e.g. dental fillings).

ClinicalTrials.gov NCT07642856