CompletedNot Applicable

Physiology of Weakness in Movement Disorders

United States6 participantsStarted 2006-03-23

Plain-language summary

This study will compare electroencephalograph (EEG) recordings in healthy volunteers and in people with movement disorders to examine brain activity associated with the weakness. EEG records the electrical activity of the brain ("brain waves"). Healthy volunteers and patients with arm or leg weakness who are between 18 and 80 years of age may be eligible for this study. Healthy subjects are screened with a medical history, physical and neurological examinations, and a questionnaire. They must be right-handed and never have had a neurological disease or head trauma. All participants have an EEG. An elastic cap with electrodes is placed on the subject's scalp to record the brain's electrical activity. During the EEG, subjects are required to resist against a force with their arm, elbow, shoulder or leg for as long as they can. Several recordings are done with short breaks between them.

Who can participate

Age range18 Years – 80 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

* INCLUSION CRITERIA: * Both patients and healthy volunteers will be between age 18 and 80. * Patients will be evaluated in the Human Motor Control Clinic at NINDS. * The definite diagnosis of the disease may not be completely established at the time of recording. * Patients have clear and reproducible symptoms of give way weakness of either upper or lower extremities. * Patients have to be able to resist against the examiner for at least two seconds before giving way. * Healthy volunteers are right handed adults without history of neurological disease or severe head trauma. EXCLUSION CRITERIA: * Subjects (patients or volunteers) who cannot understand the instructions and consent forms of the protocol will be excluded. * Subjects who cannot follow the instruction during the entire recording for whatever reason will be excluded. * Patients with a documented organic central nervous system lesion may be excluded from the study. This will be discussed in detail for each individual subject at the Human Motor Control Clinic.

Trial details

NCT IDNCT00307346

SponsorNational Institute of Neurological Disorders and Stroke (NINDS)

Sponsor typeNIH

Study typeOBSERVATIONAL