EEG and EMG Analysis of Ideomotor Apraxia
EEG Analysis of Ideomotor Apraxia
2 other identifiers
observational
60
1 country
1
Brief Summary
This study will examine how the brain operates during execution and control of voluntary movement and what goes wrong with these processes in disease. It will use electroencephalography (EEG) and electromyography (EMG) to compare brain function in normal subjects and in patients with-a disorder affecting patients with stroke and other brain lesions. These patients have problems with timing, sequence and spatial organization of certain types of movements. EEG measures the electrical activity of the brain. The activity is recorded using wire electrodes attached to the scalp or mounted on a Lycra cap placed on the head. EMG measures electrical activity from muscles. It uses wire electrodes placed on the skin over the muscles. Adult healthy normal volunteers and patients with ideomotor apraxia with a single left brain lesion may be eligible for this study. Study participants will be asked to make certain movements with their arms or hands, such as waving and using scissors. Brain and muscle activity will be measured during these tasks with EEG and EMG recordings. Patients may be asked to repeat these tests over time as their condition changes (such as during recovery from a stroke) to gain information about the recovery process.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Oct 2001
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2001
CompletedFirst Submitted
Initial submission to the registry
October 10, 2001
CompletedFirst Posted
Study publicly available on registry
October 11, 2001
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2005
CompletedMarch 4, 2008
September 1, 2005
October 10, 2001
March 3, 2008
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Normal subjects.
- Patients diagnosed with Ideomotor apraxia with a single left hemisphere lesion.
- Patients with Ideomotor apraxia with corticobasal ganglionic degeneration.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institute of Neurological Disorders and Stroke (NINDS)
Bethesda, Maryland, 20892, United States
Related Publications (1)
Bannur U, Rajshekhar V. Post operative supplementary motor area syndrome: clinical features and outcome. Br J Neurosurg. 2000 Jun;14(3):204-10. doi: 10.1080/026886900408379.
PMID: 10912196BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Sponsor Type
- NIH
Study Record Dates
First Submitted
October 10, 2001
First Posted
October 11, 2001
Study Start
October 1, 2001
Study Completion
September 1, 2005
Last Updated
March 4, 2008
Record last verified: 2005-09