Phase
Condition
Stroke
Thrombosis
Cerebral Ischemia
Treatment
Non-invasive Electrical Spinal Cord Stimulation
Activity Based Rehabilitation
Clinical Study ID
Ages 21-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Radiologically documented single ischemic stroke resulted in hemiplegia/hemiparesis
At least six months post-stroke
Upper Extremity Fugl-Meyer Assessment score "moderate" or "moderate-mild" (29-53inclusive out of 66) at the screening visit
Medically and neurologically stable, as determined by medical history and documentedphysical examination
For women of childbearing potential, a negative over-the-counter pregnancy test atstudy entry and willingness to practice adequate contraception during the study
Ability to attend sessions three times per week
Adequate social support to participate in all intervention and baseline, follow-upassessment sessions throughout eight months.
Ability to read, comprehend and speak English
Exclusion
Exclusion Criteria:
Hemorrhagic stroke
History of multiple strokes
Active implanted stimulator (e.g., pacemaker, vagus nerve stimulator, cochlearimplant, etc.) or baclofen pump
Aphasia or any other deficit in communication that interferes with reasonable studyparticipation
Moderate to severe cognitive impairment
Presence of neglect (inability to perceive or awareness of, or loss of attention tothe weaker half of the body)
Severe spasticity in the upper limb
Taking baclofen more than 30 mg/day
Change in baclofen dose within four weeks before enrollment
Receiving benzodiazepines, dantrolene, tizanidine, anticoagulant, or antiepilepticmedication
Botulinum toxin injection to the upper limb muscles within six months beforeenrollment
Severe joint contractures in the affected hand and arm
History of spontaneous seizure that had occurred one month or longer after thestroke
Study Design
Connect with a study center
University of Washington
Seattle, Washington 98105
United StatesActive - Recruiting

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