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Sponsored by: |
National Institute of Neurological Disorders and Stroke (NINDS) |
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Information provided by: | National Institutes of Health Clinical Center (CC) |
ClinicalTrials.gov Identifier: | NCT00001216 |
This study is designed to allow researchers to use transelectrical stimulation to explore the function of the human nervous system and improve diagnosis of neurological disorders.
Transcranial electrical stimulation is a non-invasive technique that can be used to stimulate brain activity and gather information about brain function. Electrical stimulation involves placing electrodes on the scalp or skin and passing an electrical current between them. When this is done, an electrical field is created that activates areas of the brain that control muscles. Muscle activity as a result of the stimulation can be recorded and analyzed.
Condition |
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Cerebrovascular Disorders Healthy Nervous System Diseases Spinal Cord Injuries |
Study Type: | Observational |
Official Title: | Non-Invasive Stimulation of the Human Central Nervous System (Digitimer) |
Estimated Enrollment: | 175 |
Study Start Date: | February 1986 |
Estimated Study Completion Date: | February 2001 |
This protocol application is written to permit us to use transcranial electrical stimulation, a safe and noninvasive method for activating the brain, spinal cord, or proximal nerves through the skin, in appropriate subjects. We will use this technique to explore the function of the human central and peripheral nervous system and to aid in the diagnosis of neurological disorders.
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Males and females, ages 18 and over.
Diverse racial groups.
Amputees and others with whom we will have no patient-care relationship may also be considered to be volunteers.
Patients will be recruited from those referred to the Human Motor Control Section, NINDS who have neurological syndromes that are of interest.
On rare occasions we may attempt to study children as young as 10 years with TES.
Individuals without indwelling cardiac lines and pacemakers.
Patients recruited for study would come from those referred to the EMG laboratory and to the Human Motor Control Clinic who would have distinct neurologic syndromes from well defined peripheral and central nervous system lesions including hemiplegia from stroke, trauma, tumor or focal demyelination (most commonly patients would have hemiplegia from stroke), peripheral nerve lesions, amputations, spinal cord injury.
Normal volunteers, including NIH employees, would be healthy adults without history of physical examination evidence of neurologic disease and individuals with different types of amputations involving upper and lower extremities.
Volunteers may also be participants in the electrophysiological protocol (84-N-0196).
No history of epilepsy.
Study ID Numbers: | 860020, 86-N-0020 |
Study First Received: | November 3, 1999 |
Last Updated: | March 3, 2008 |
ClinicalTrials.gov Identifier: | NCT00001216 |
Health Authority: | United States: Federal Government |
Amputations Brainstem Stimulation Cerebellar Stimulation Cortical Motor Physiology Electrical Stimulation |
Motor Cortex Plasticity Spinal Cord Injury Stroke |
Spinal Cord Injuries Spinal Cord Diseases Cerebral Infarction Stroke Wounds and Injuries Vascular Diseases |
Disorders of Environmental Origin Central Nervous System Diseases Healthy Trauma, Nervous System Brain Diseases Cerebrovascular Disorders |
Nervous System Diseases Cardiovascular Diseases |