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Neuro-Intermuscular Coordination Enhancement (NICE) Rehabilitation Through Human-Machine Interaction in Chronic Stroke

Sponsored by University of Houston

About this study

The objective of this study is to develop Neuro-Intermuscular Coordination Enhancement (NICE) rehabilitation, a novel neuromuscular control signal-guided strategy that visually guides stroke patients to individually activate motor modules through human-machine interaction. Ultimately, the development will lead to better clinical motor recovery, better quality of life, and lowered healthcare costs associated with the impairment.

Stroke is the leading cause of severe long-term disability, affecting 9.4 million Americans. Each year around 800,000 people suffer a stroke even in the USA. Chronic upper extremity motor impairment is a major contributing factor to disability; functional use of the affected UE in daily life is a key factor for increased independence, return to work, and overall quality of life. Thus, effective and innovative treatment to address long-term disability is both a major public health need and an economic necessity. This study is an early-stage, randomized controlled rehabilitation trial designed to evaluate the clinical effects, feasibility, transfer of therapeutic gains, and exploratory neurophysiological correlates of Neuro-Intermuscular Coordination Enhancement (NICE) in individuals with c…

Where this study is enrolling

Who can participate

Inclusion criteria

  • ✓for individuals after stroke are:
  • ✓Hemiparetic chronic stroke survivors more than 6 months after stroke onset
  • ✓Adults aged 21-80 years, including both female and male participants
  • ✓Individuals with a single unilateral ischemic or hemorrhagic stroke
  • ✓Individuals with Upper Extremity Fugl-Meyer Assessment score between 10 and 59 out of 66
  • ✓Individuals who have not received botulinum toxin injections in the upper extremity within the past 3 months
  • ✓Individuals without severe spasticity, defined as Modified Ashworth Scale score ≤3 at the elbow and shoulder

Exclusion criteria

  • ✕for individuals after stroke are:
  • ✕Individuals younger than 21 years of age or older than 80 years of age
  • ✕Individuals with an orthopedic disorder involving the upper limbs
  • ✕Individuals unable to produce voluntary upper-extremity muscle EMG activity;
  • ✕Individuals with cognitive impairment sufficient to interfere with informed consent or successful completion of the protocol, assessed using the Montreal Cognitive Assessment or other IRB-approved screening procedures.
  • ✕Individuals whose stroke-affected arm has an intermuscular coordination pattern similarity score \>0.80 relative to the non-affected arm
  • ✕Inclusion criteria for healthy individuals are:
  • ✕Healthy adults aged 21-80 years, including both female and male participants
  • ✕Individuals with no known neurological or orthopedic injuries
  • ✕Exclusion criteria for healthy individuals are:
  • ✕Individuals younger than 21 years of age or older than 80 years of age
  • ✕Individuals with known neurological disorders
  • ✕Individuals with orthopedic injuries or conditions affecting upper-extremity movement
  • ✕Individuals unable to provide informed consent

Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.

Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.

Trial data sourced from ClinicalTrials.gov.