EEG and EMG Analysis of Ideomotor Apraxia
Ideomotor Apraxia
About this trial
This is an observational trial for Ideomotor Apraxia focused on measuring Movement, Coordination, Correlation, Coherence, Parietofrontal Circuitry, Apraxia, Ideomotor Apraxia, Healthy Volunteer, HV, Normal Control
Eligibility Criteria
We will study normal volunteers and patient groups between the ages of 18-80 years of age within the following parameters: INCLUSION CRITERIA: Normal subjects. Patients diagnosed with Ideomotor apraxia with a single left hemisphere lesion. Patients with Ideomotor apraxia with corticobasal ganglionic degeneration. EXCLUSION CRITERIA Normal subjects: abnormal neurologic examination or history of neurologic disorders. Ideomotor apraxic patients: a second neurologic disorder including more than one brain lesion or the inability to cooperate fully. Normal and Ideomotor apraxic patients: cognitively impaired subjects will not be accrued (for the purposes of this study, patients that can provide full informed consent for the study are not considered cognitively impaired). For MRI studies, patients with metallic implants to remove potential risks from this procedure. For MRI purposes, women who are pregnant are excluded from this part of the protocol. Therefore, all women of childbearing potential will have a pregnancy test performed, which must be negative, before proceeding.
Sites / Locations
- National Institute of Neurological Disorders and Stroke (NINDS)