There are over 7 million stroke survivors in the US alone, with approximately 795,000 new cases annually. Despite the best available physiotherapy, 30-60% of stroke survivors remain affected by difficulty walking, with foot weakness often being the main cause. Given that post-stroke gait impairments remain poorly addressed, new methods that can provide lasting improvements are necessary. Brain-computer interface (BCI) technology may be one such novel approach. BCI technology enables "direct brain control" of external devices such as assistive devices and prostheses by translating brain waves into control signals. When BCI systems are integrated with functional electrical stimulation (FES) systems, they can be used to deliver a novel physical therapy to improve movement after stroke. BCI-FES systems are hypothesized to stimulate recovery after stroke beyond that of conventional physical therapy.
Brain Computer Interface - Functional Electrical Stimulation (BCI-FES) Therapy for Stroke Rehabilitation
Preliminary research indicates that applying this technique to foot weakness after stroke is safe and may improve walking function. Hence, this warrants further investigation to: 1. determine if BCI-FES therapy can provide lasting gains in walking in chronic stroke patients; 2. determine what factors influence BCI-FES therapy; and 3. explicitly elucidate the underlying neural repair mechanisms. First, a Phase II clinical trial in patients with foot drop due to chronic stroke will compare the effect of BCIFES dorsiflexion therapy to that of dose- and intensity-matched standard physical therapy (Aim 1). Comparing the improvement in walking speed and other secondary outcome measures between the two groups will test if BCI-FES therapy provides functional and neurological gains beyond those of standard physical therapy. The relationship between the patient baseline characteristics (walking speed, ankle function, stimulated muscle responses, brain wave features, sensation) and the outcomes will determine what features influence responsiveness to BCI-FES dorsiflexion therapy (Aim 2). Finally, the underlying mechanism driving the improvements of BCI-FES will be studied (Aim 3). Determining that BCI-FES therapy can provide improvements beyond that of standard therapy may lead to a new treatment for stroke patients. The underlying mechanism can inform the design of future physical therapy techniques or improve current ones. Finally, BCI-FES therapy may ultimately become a novel form of physical therapy to reduce post-stroke disability, and in turn reduce the public health burden of stroke.
Ischemic Stroke Hemorrhagic Stroke stroke BCI-FES dorsiflexion therapy Physiotherapy one hour Physiotherapy two hours Dose-and intensity-matched physiotherapy
You can join if…
Open to people ages 18-80
- Age18-80 years inclusively at time of consent;
- Radiologically confirmed first unilateral stroke, ischemic or intracranial hemorrhage (ICH) in etiology, with day of onset 26-104 weeks prior to day of randomization
- Gait velocity<0.8 m/s at screening and baseline visits;
- Foot-drop in affected limb as defined by dorsiflexion active range of motion (AROM) via goniometry in seated position foot dangling is less than passive range of motion and less than 15 degrees.
- Plantarflexors spasticity<3 on modified Ashworth Scale;
- Can walk >10 m (no ankle foot orthosis (AFO), but cane or walker permitted) at a supervised level;
- Can tolerate FES with pain no more than 4 on pain analog scale and has adequate muscle response of TA dorsiflexion ≥10 degrees;
- Passive Range of Motion at least +10 degrees ankle dorsiflexion in subtalar neutral
You CAN'T join if...
- A major, active, coexistent medical, neurological (apart from stroke) or psychiatric disease (apart from stroke), including alcoholism or dementia, orthopedic injuries, that substantially affects gait.
- A major medical disorder that substantially reduces the likelihood that a subject will be able to comply with all study procedures or safely complete study procedures. This includes, but not limited to documented serious cardiac conditions, serious pulmonary conditions, legal blindness, end stage renal or liver disease, pulmonary embolism or deep venous thrombosis.
- Resting systolic blood pressure above 170, diastolic blood pressure above 100 at screening and baseline evaluations
- Implanted electronic device (e.g. pacemaker) or skull metallic implants (e.g. cranioplasty plate);
- Deficits in communication that interfere with reasonable study participation: language or attention impairment (score>1 on NIH Stroke Scale items 9 and 11, respectively)
- Significant cognitive impairment, defined as Montreal Cognitive Assessment score < 22 (For those with aphasia: **Because Montreal Cognitive Assessment scores may be difficult to interpret for patients with aphasia, at the discretion of the site's study PI, exclusion criterion #5 ("MoCA score cannot be <22") can be waived)6. A new symptomatic stroke occurs apart from the index stroke during the screening process and prior to randomization
- Life expectancy < 6 months
- Skin breakdown over electrical stimulation sites;
- Received chemical denervation (eg Botox) to arms, legs, or trunk in the preceding 6 months, or expectation that chemical denervation will be administered to the arm, leg, or trunk prior to expected completion of the study
- . Unable or unwilling to perform study procedures/therapy, or expectation of non-compliance with study procedures/therapy
- . Pregnancy;
- . Significant pain (visual analog scale >4), chest pain, or shortness of breath with walking.
- . Receiving any outside concurrent physical therapy
- . Any general medical condition and psychosocial situation that substantially interferes with reasonable participate in study appointments
- . Non-English speaking, such that subject does not speak sufficient English to comply with study procedures
- . Concurrent enrollment in another investigational interventional study
- . Severe depression, defined as Geriatric Depression Scale Score >11
- . Prior or concurrent use of FES orthosis for gait.
- . A new symptomatic stroke occurs apart from the index stroke during the screening process and prior to randomization
If TMS Eligible (note that potential subjects who do not qualify for TMS will not be excluded from the main study, they will only be excluded from undergoing TMS procedures):
- . TMS: Metallic hardware on the scalp (e.g. vascular clips or cranioplasty mesh)
- . TMS: Implanted medication pumps, intracardiac line, or central venous catheter
- . TMS: History of cortical stroke or other cortical lesion such as brain tumor
- . TMS: Prior diagnosis of seizure or epilepsy
- . TMS: Any electrical, mechanical, or magnetic implants
- . TMS: History of neurosurgery
- . TMS: uncontrolled Migraine headaches
- . TMS: Any current medications that affect seizure threshold such as tricyclic antidepressants and neuroleptics
- . TMS: Unstable medical conditions
- University of California, Irvine - Sue & Bill Gross Stem Cell Research Center
accepting new patients
Irvine California 92697 United States
Lead Scientist at UC Irvine
- An Do, MD
Assistant Health Sciences Professor, Neurology. Authored (or co-authored) 31 research publications.
- accepting new patients
- Start Date
- Completion Date
- University of California, Irvine
- Study Type
- Last Updated
Please contact me about this study
We will not share your information with anyone other than the team in charge of this study. Submitting your contact information does not obligate you to participate in research.
The study team should get back to you in a few business days.