Status:

COMPLETED

Improving Hand Movement Training Through Electrical Stimulation of the Brain

Lead Sponsor:

National Institute of Neurological Disorders and Stroke (NINDS)

Conditions:

Metaplasticity

Eligibility:

All Genders

18-50 years

Brief Summary

This study will determine if applying electrical stimulation of the brain can influence training to perform finger movements. The study may provide information that can be used to design rehabilitatio...

Detailed Description

OBJECTIVES: Training leads to performance improvements and motor learning. Cortical plasticity associated with training (use-dependent plasticity, UDP) contributes to performance improvements after b...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:
  • age between 18-50 years
  • able to perform tasks required by the study
  • willing and able to give consent
  • willing to make an eight-week commitment to the study
  • possibility of obtaining TMS-evoked thumb movements in a consistent direction at baseline
  • EXCLUSION CRITERIA:
  • unable to perform the tasks
  • history of severe alcohol or drug abuse, psychiatric illness such as severe depression, poor motivational capacity, or severe language disturbances, particularly of receptive nature or with serious cognitive deficits (defined as equivalent to a mini-mental state exam score (MMSE) of 23 or less), or degenerative brain processes such as Alzheimer's disease
  • severe uncontrolled medical problems (e.g., cardiovascular disease, severe rheumatoid arthritis, active joint deformity of arthritic origin, active cancer or renal disease, any kind of end-stage pulmonary or cardiovascular disease, or a deteriorated condition due to age, uncontrolled epilepsy or others), more than moderate to severe microangiopathy, polyneuropathy, diabetes mellitus, or ischemic peripheral disease
  • problems with movement of the hands
  • receiving drugs acting primarily on the central nervous system, which lower the seizure threshold such as antipsychotic drugs (chlorpromazine, clozapine) or tricyclic antidepressants (for the TMS component)
  • pregnancy and during lactation
  • medical or technical contraindications to MRI procedures or devices producing artifacts that impair MRI signal (e.g., dental braces, pacemakers, implanted medication pumps, cochlear devices, neural stimulators, metal in the cranium, surgical clips, and other metal/magnetic implants, claustrophobia)

Exclusion

    Key Trial Info

    Start Date :

    May 24 2006

    Trial Type :

    OBSERVATIONAL

    End Date :

    April 21 2008

    Estimated Enrollment :

    31 Patients enrolled

    Trial Details

    Trial ID

    NCT00331318

    Start Date

    May 24 2006

    End Date

    April 21 2008

    Last Update

    July 2 2017

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    National Institutes of Health Clinical Center, 9000 Rockville Pike

    Bethesda, Maryland, United States, 20892