Novel Brain Stimulation Therapies in Stroke Guided Expressions of Plasticity



Status:Recruiting
Conditions:Peripheral Vascular Disease, Cardiology, Neurology, Neurology, Neurology
Therapuetic Areas:Cardiology / Vascular Diseases, Neurology
Healthy:No
Age Range:21 - Any
Updated:3/10/2019
Start Date:March 2016
End Date:December 2019
Contact:Ela Plow, PhD, PT
Email:plowe2@ccf.org
Phone:216-4454589

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The investigators ultimate goal is to personalize brain stimulation for stroke so outcomes of
the upper limb can be maximized for each individual patient. Several groups including the
investigators have recently theorized that personalizing stimulation so as to selectively
stimulate iM1 in mild, and cPMd in patients with greater severity would help generalize
benefits of stimulation. The investigator premise that variances in expressions of plasticity
can explain how to best stratify patients for robust, personalized stimulation.

AIMS: The ultimate goal is to personalize brain stimulation for stroke so outcomes of the
upper limb can be maximized for each individual patient. Even though stimulation is one of
the most well studied methods to augment plasticity and boost recovery, it is still not
approved for outpatient therapy. Benefits of stimulation are weak and variable especially in
patients who suffer from greater damage and disability. The key limitation of the standard
approach is its generic assumptions about plasticity. The current standard assumes that
ipsilesional primary motor cortex (iM1) can impact recovery for patients in all ranges of
severity, and intact, contralesional cortices always compete with iM1 to inhibit recovery.
But, these long-standing assumptions fail to consider that iM1 or its pathways are damaged in
a majority (58-83%) of patients. As such, the potential of iM1 would be weak and variable,
and patients will have little option but to rely on plasticity of intact, contralesional
cortices that are more likely to survive. Of all surviving cortices, contralesional dorsal
premotor cortex (cPMd) expresses plasticity most consistently. cPMd is activated in movement
of the paretic limb when activating iM1 is less likely. cPMd even reduces its competition
with iM1 and offers its ipsilateral pathways instead to support recovery of the proximal
paretic limb when pathways from iM1 are largely damaged.

Several groups including the investigator have recently theorized that personalizing
stimulation so as to selectively stimulate iM1 in mild, and cPMd in patients with greater
severity would help generalize benefits of stimulation. These theoretical claims, however,
remain untested since several gaps exist. For instance, what is the cut-off level of severity
that stratifies those who respond to stimulation of iM1 from those who respond to stimulation
of cPMd? Even then, are substrates for 'personalized' stimulation same as the substrates that
express plasticity in recovery, i.e. if patients benefit from stimulation of cPMd, do they
express contralesional plasticity in recovery? Here, the investigator premise that variances
in expressions of plasticity can explain how to best stratify patients for robust,
personalized stimulation.

Inclusion Criteria:

- greater than 21 years old

- more than 6 months from first, unilateral index stroke

- unilateral paresis of the upper limb indexed as greater than or equal to 20% slowness
in functional reaching compared to non-paretic limb

- UEFM less than or equal to 61 out of 66.

Exclusion Criteria:

- subjects who cannot perform reaching with shoulder

- severe cognitive deficit (less than or equal to 24 on Mini-Mental State examination.

- contraindication to TMS or MRI including: seizures, ongoing use of certain neuro- or
psycho-active medications, implants, or pacemaker.

- currently receiving outpatient therapy.
We found this trial at
1
site
2049 E 100th St
Cleveland, Ohio 44106
(216) 444-2200
Phone: 216-445-4589
Cleveland Clinic Foundation The Cleveland Clinic (formally known as The Cleveland Clinic Foundation) is a...
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mi
from
Cleveland, OH
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