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Clinical Trials/NCT06598150
NCT06598150
Recruiting
N/A

Mapping Corticoreticulospinal Motor Control Using Brainstem and Spinal Cord fMRI in Chronic Hemiparetic Stroke

Northwestern University1 site in 1 country32 target enrollmentMay 20, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stroke
Sponsor
Northwestern University
Enrollment
32
Locations
1
Primary Endpoint
BOLD activation
Status
Recruiting
Last Updated
7 months ago

Overview

Brief Summary

This study uses functional magnetic resonance imaging to map neural activity throughout the central nervous system during a shoulder abduction task to characterize what motor pathways are being used post-stroke.

Detailed Description

Nearly 85% of stroke survivors experience significant unilateral impairment in upper extremity motor control, typically caused by damage to the corticospinal (CST) and corticoreticular (CRT) tracts (i.e., the corticofugal tracts). Alternative neural pathways, such as the contralesional cortico-reticulospinal tract (CRST), can be recruited to achieve movement of the affected arm and hand, but may have undesirable consequences. For example, the diffuse, bilateral branching of reticulospinal neurons can produce abnormal muscle co-activations (synergies) in the paretic limb, and involuntary mirror movements (associated reactions) between limbs. Together, these effects create stereotypical movement patterns post-stroke, and there is growing interest in novel \"anti-synergy\" interventions to enhance usage of residual CST systems rather than strengthening the CRST. Imaging has the potential to become an invaluable tool for evaluating whether rehabilitative strategies can preferentially access CST versus CRST pathways. However, current functional imaging research has focused on cortical activity, and must theoretically infer what pathway is used. Structural MRI directly assesses changes in white matter pathways, but it is limited to detecting long-term plasticity. To guide new interventions, there is a critical need to directly evaluate what descending motor pathways are active during movement. Thus, the overall objective of this study is to generate a novel fMRI dataset in participants with post-stroke hemiparesis, capturing neural activity during an innovative isometric shoulder abduction task, evaluating differences when abducting the paretic versus non-paretic arm. The investigators will acquire multi-echo fMRI data in individuals with post-stroke hemiparesis and age-matched controls, hypothesizing that increased reliance on the CRST will cause distinct activation patterns during shoulder abduction with the paretic limb, and that this will correlate with individual upper-extremity impairment (Upper-Extremity Fugl-Meyer Assessment). This work is significant because it will provide direct evidence of descending contralesional motor pathway involvement in post-stroke hemiparesis, and demonstrate the utility of neuroimaging for optimizing movements to preferentially engage specific systems and promote desired neural plasticity following injury.

Registry
clinicaltrials.gov
Start Date
May 20, 2023
End Date
August 31, 2026
Last Updated
7 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Molly Bright

Assistant Professor

Northwestern University

Eligibility Criteria

Inclusion Criteria

  • Adults aged at least 18y
  • Able to perform shoulder abduction task (confirmed during screening and initial examination)
  • Safe to undergo MRI
  • Able to follow visual instructions using MRI-compatible vision correction goggles
  • No brainstem or cerebellar lesions
  • No severe concurrent medical problems
  • Cognitive/attentional capacity to focus on a task
  • Able to communicate in English or Spanish
  • Additional inclusion criteria for stroke participants:
  • Have sustained only one unilateral subcortical, ischemic lesion in the territory supplied by the Middle Cerebral Artery (confirmed by clinical or radiological reports) at least one year prior to participation in this project

Exclusion Criteria

  • MRI contraindications
  • Severe claustrophobia
  • Pregnant women
  • Prisoners
  • Vulnerable populations
  • Diagnosis/history of:
  • multiple sclerosis
  • brain tumor
  • brain radiation
  • traumatic brain injury

Outcomes

Primary Outcomes

BOLD activation

Time Frame: 3 days to 3 months

BOLD fMRI data will be analyzed to map neural activation associated with the shoulder abduction task.

Study Sites (1)

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