Brain Connections for Arm Movement After Stroke

  • STATUS
    Recruiting
  • participants needed
    6
  • sponsor
    VA Pittsburgh Healthcare System
Updated on 19 February 2024
transcranial magnetic stimulation
cardiovascular disease
stroke
neurological disorder

Summary

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.

Description

The general objective of this application is to study reorganization of network interactions following a common type of subcortical stroke (i.e. internal capsule) with mechanistic studies using noninvasive neurophysiology in humans. The goal is to obtain pilot data and to demonstrate the feasibility of the approach that combines transcranial magnetic stimulation (TMS) with reaching in an advanced exoskeleton robot. As reaching is an essential part of many daily activities, this approach will have beneficial impacts on the quality of life of these stroke patients.

The central hypothesis is that bilateral premotor cortical areas, dorsal (PMd) more so than ventral (PMv,) develops greater connectivity with primary motor cortex (M1) after stroke and thus better ability to produce motor outputs that support reaching with the paretic arm. When there is more damage to the corticospinal tract, contralesional areas will take on a greater role.

The relationship between connectivity, behavioral effects of stimulation and motor performance will be established. These findings will allow the investigators to formulate clear hypotheses about which premotor area should be modulated with TMS, depending on stroke extent and deficits in motor control, when reaching the stage of proposing a treatment trial. Increased knowledge of the dynamic changes of physiological interactions during various phases of reaching movements will allow a more defined study regarding the role of premotor areas in recovery of motor function after stroke, and a novel treatment protocol that delivers precisely timed stimulations during practice of reaching movements. Ultimately, the investigators can test these novel treatments in clinical trials and compare their impact to other, less specific, neuromodulatory methods such as transcranial direct current stimulation. This study will also lay the groundwork for collaboration in brain computer interface and non-human primate investigations in the mechanisms and treatment of motor deficits after stroke.

Details
Condition Brain Diseases, CNS disorder, Cerebrovascular accident, nervous system disorder, Cardiovascular Disease
Age 45years - 90years
Treatment Transcranial magnetic stimulation
Clinical Study IdentifierNCT04286516
SponsorVA Pittsburgh Healthcare System
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

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

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
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