NCT00024999

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Oct 2001

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2001

Completed
9 days until next milestone

First Submitted

Initial submission to the registry

October 10, 2001

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 11, 2001

Completed
3.9 years until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2005

Completed
Last Updated

March 4, 2008

Status Verified

September 1, 2005

First QC Date

October 10, 2001

Last Update Submit

March 3, 2008

Conditions

Keywords

MovementCoordinationCorrelationCoherenceParietofrontal CircuitryApraxiaIdeomotor ApraxiaHealthy VolunteerHVNormal Control

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

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

Location

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

Apraxia, IdeomotorApraxias

Condition Hierarchy (Ancestors)

Psychomotor DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

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

Locations