Study of Brain Control of Movement

Sponsor
National Institute of Neurological Disorders and Stroke (NINDS) (NIH)
Overall Status
Completed
CT.gov ID
NCT00017979
Collaborator
(none)
30
1
12
2.5

Study Details

Study Description

Brief Summary

This study will use transcranial magnetic stimulation to examine how the brain controls movement by sending messages to the spinal cord and muscles and what goes wrong with this process in disease. Normal healthy volunteers between the ages of 18 and 65 years may be eligible to participate.

In transcranial magnetic stimulation, an insulated wire coil is placed on the subject's scalp or skin. Brief electrical currents are passed through the coil, creating magnetic pulses that stimulate the brain. During the stimulation, participants will be asked to tense certain muscles slightly or perform other simple actions. The electrical activity of the muscle will be recorded on a computer through electrodes applied to the skin over the muscle. In most cases, the study will last less than 3 hours.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The purpose of this study is to investigate the influence of voluntary inhibition of movement, using either negative motor imagery or Go/NoGo reaction task, on cortical inhibitory mechanisms. Intracortical inhibition (ICI) and silent period (SP) are two major cortical inhibitory mechanisms demonstrated by transcranial magnetic stimulation (TMS). Alterations in these inhibitory mechanisms have been extensively studied in various situations, but the influence of voluntary inhibition has not been elucidated yet. In normal volunteers, therefore, we plan to determine if voluntary inhibition of movement influences these cortical inhibitory mechanisms. The primary outcome measures would be any changes in motor evoked potential (MEP) size and intracortical inhibition (ICI) parameters.

    Study Design

    Study Type:
    Observational
    Official Title:
    Effect of Volitional Inhibition on Cortical Inhibitory Mechanisms
    Study Start Date :
    Jun 1, 2001
    Study Completion Date :
    Jun 1, 2002

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      N/A and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes

      Volunteers who are greater than or equal to 18 years old.

      Subjects must not have any medico-surgical illness.

      Subjects must not have neurological illness.

      Subjects must not have psychiatric illness.

      Subjects must not be taking any medication with potential

      influence on nervous system function.

      Subjects must not have a pacemaker.

      Subjects must not have an implanted medical pump.

      Subjects must not have a metal plate or a metal object in the skull or eye.

      Subjects must not have a history of seizure disorder.

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 National Institute of Neurological Disorders and Stroke (NINDS) Bethesda Maryland United States 20892

      Sponsors and Collaborators

      • National Institute of Neurological Disorders and Stroke (NINDS)

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00017979
      Other Study ID Numbers:
      • 010200
      • 01-N-0200
      First Posted:
      Jun 25, 2001
      Last Update Posted:
      Mar 4, 2008
      Last Verified:
      Jun 1, 2002

      Study Results

      No Results Posted as of Mar 4, 2008