Actively Recruiting
rTMS Plus CCFES-mediated Functional Task Practice for Severe Stroke
Led by The Cleveland Clinic · Updated on 2026-03-24
72
Participants Needed
1
Research Sites
398 weeks
Total Duration
On this page
Sponsors
T
The Cleveland Clinic
Lead Sponsor
E
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study is a necessary and important step in the development of a new therapy for upper limb functional recovery in patients with severe motor impairment. It is the first clinical trial of non-invasive brain stimulation (repetitive transcranial magnetic stimulation or rTMS) delivered to excite the undamaged hemisphere (specifically the contralesional higher motor cortices or cHMC) in stroke. Therefore, this study will determine whether the positive results obtained in our short-term pilot study can be made to last longer and produce functional benefits in severe patients with the application of brain stimulation in combination with long-term rehabilitation therapy. Rehabilitation therapy administered is called contralaterally controlled functional electrical stimulation (CCFES). Determining whether combining rTMS facilitating the cHMC with CCFES produces synergistic gains in functional abilities in severe patients is necessary for acceptance by the clinical community and to move this technology toward commercialization and widespread dissemination. The proposed study will determine whether the combination of rTMS facilitating the cHMC with CCFES produces greater improvements in upper extremity function in severe participants who are ≥6 months from stroke onset than the combination of rTMS facilitating the damaged hemisphere (specifically the ipsilesional primary motor cortex, iM1) and CCFES or the combination of sham rTMS and CCFES. The secondary purposes are to define which patients benefit most from the treatments, which may inform future device and treatment development and clinical translation, and to explore what distinct effects the three treatments have on the brain. To accomplish these purposes, we are conducting a clinical trial that enrolls severe stroke patients.
CONDITIONS
Official Title
rTMS Plus CCFES-mediated Functional Task Practice for Severe Stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 to 90 years old at time of randomization
- More than 6 months since a first clinical cortical or subcortical ischemic or hemorrhagic stroke
- Severe upper limb hemiparesis defined as less than 10 degrees active wrist extension or thumb abduction/extension or less than 10 degrees active extension in at least two additional digits
- Ability to follow 3-stage commands and remember 2 items from a list of 3 after 3 minutes
- Adequate shoulder and elbow movement to position the affected hand on the lap for exercises
- Skin intact on the affected arm
- Surface electrical stimulation produces functional hand opening without pain
- Able to hear and respond to cues from the stimulator
- Completed occupational therapy at least 2 months prior with no concurrent therapy
- Full voluntary hand opening and closing of the unaffected hand
- Ability to follow instructions for using the CCFES stimulator or have caregiver assistance
You will not qualify if you...
- Metal implant in the head
- History of seizures as an adult
- History of alcohol or substance abuse within 10 years prior to enrollment
- Taking anticonvulsants or antidepressants that are contraindicated with TMS
- Cardiac pacemaker or other programmable implant
AI-Screening
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Trial Site Locations
Total: 1 location
1
Lerner Research Institute; Cleveland Clinic Foundation
Cleveland, Ohio, United States, 44195
Actively Recruiting
Research Team
K
Kyle J. O'Laughlin, MS
CONTACT
E
Ela B. Plow, PhD PT
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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