About this trial
The goal of this research study is to optimize the parameter of Low-Intensity Focused Ultrasound Stimulation (LIFUS) that is most effective in changing cortical excitability and motor learning skills in patients who suffered a stroke. The researchers hope to answer two questions.
* with increasing power, would LIFUS be more effective? * with the same power, what LIFUS timing is the best
For Aim 1, the study will compare 8, 4 W/cm\^2 to a zero(sham) stimulation to see if higher power is the better.
For Aim 2, the study will compare 500 vs 1000 vs 2000 Hz "timing" to see which one is better.
Eligibility criteria
Qualifiers
age >=21 years old of any gender or race
First-ever ischemic or hemorrhagic stroke (neuroimaging verified) at least 6 months from the stroke onset of symptoms
Unilateral arm weakness measured by the Fugl-Meyer Upper-Extremity Scale ≤ 62/64
Inducible rest motor threshold and testing motor threshold recorded from the affected abductor pollicis brevis muscle
Disqualifiers
Bilateral strokes (infarcts and/or hematoma)
Other co-existent neuromuscular disorders affecting upper extremity motor impairment
History of medically uncontrolled depression or other neuropsychiatric disorders despite medications either before or after a stroke that may affect the subject's ability to participate in the study
History of confirmed dementia or taking dementia drugs
Trial design
Treatments tested in this trial
- Low intensity focused ultrasound stimulation
Treatment groups
6
Treatment groupsSee each treatment group below.