Non-Invasive Stimulation of the Human Central Nervous System (Digitimer)
Data Collection
Brain Diseases+8
+ Cardiovascular Diseases
+ Central Nervous System Diseases
Summary
Study start date: February 1, 1986
Actual date on which the first participant was enrolled.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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.175 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
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 Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
National Institute of Neurological Disorders and Stroke (NINDS)
Bethesda, United StatesOpen National Institute of Neurological Disorders and Stroke (NINDS) in Google Maps