Stroke Clinical Trial
— CAMOfficial title:
Brain Areas That Control Reaching Movements After Stroke: Task-relevant Connectivity and Movement-synchronized Brain Stimulation
The purpose of this study is to use Transcranial Magnetic Stimulation (TMS) while subjects are making reaching movements in a robotic arm device in order to discover how different brain areas control movement before and after stroke and when these brain areas are most sensitive to TMS.
Status | Recruiting |
Enrollment | 17 |
Est. completion date | June 1, 2026 |
Est. primary completion date | June 1, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 45 Years to 90 Years |
Eligibility | Inclusion Criteria: Inclusion Criteria (control participants): - Be 45-90 years of age - Have adequate language and neurocognitive function to participate in training and testing - Be medically stable to participate in the study - Be English speaking Inclusion Criteria (participants with stroke): - Be 45-90 years of age - Clinically defined, unilateral, hemiparetic stroke with radiologic exclusion of other possible diagnosis - Stroke onset at least 6 months before enrollment - Subcortical stroke (ex: internal capsule, deep white matter of posterior frontal lobe) - Present with mild to moderate arm dysfunction - Be medically stable to participate in the study - Be English speaking Exclusion Criteria: (for both groups) - Unable to give informed consent - Have a serious complicating medical illness that would preclude participation - Contractures or orthopedic problems limiting range of joint motion in the potential study arm or other impairments that would interfere with the study activities - Visual loss such that the subject would not be able to see the test patterns on the robot computer monitor - Unable to comply with requirements of the study - Enrollment in another greater-than-minimal risk study - Presence of medical condition or implant that prevents safe administration of TMS or MRI - Pregnancy |
Country | Name | City | State |
---|---|---|---|
United States | VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
VA Office of Research and Development | University of Pittsburgh, VA Pittsburgh Healthcare System |
United States,
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Path length | Movement path length in centimeters from KINARM system during the one second reaching period. (units: cm) | Immediate (within 2 s after stimulation) | |
Secondary | Times | Specific kinematic data from KINARM system: reaction time, movement time to reach target (units: ms) | Immediate (within 2 s after stimulation) | |
Secondary | Velocities | maximum velocity reached during reach (units: cm/s) | Immediate (within 2 s after stimulation) | |
Secondary | Accuracy | specific position data from KINARM system: target accuracy, distance from manipulandum position at end of one second reaching period to target center. (units: cm.) | Immediate (within 2 s after stimulation) | |
Secondary | EMG | Electromyographic data from surface electrodes on biceps, triceps, anterior deltoid, and posterior deltoid muscles - These signals will be rectified and normalized to the maximum values during practice reaches. (units: mV/mV - dimensionless). | Immediate (within 2 s after stimulation) |
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