Actively Recruiting
Increasing the Repertoire of Intermuscular Co-ordination Post Stroke Through EMG-Guided Human-Machine Interaction
Led by University of Houston · Updated on 2026-05-04
74
Participants Needed
1
Research Sites
256 weeks
Total Duration
On this page
Sponsors
U
University of Houston
Lead Sponsor
K
Korea Advanced Institute of Science and Technology
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purposes of this study include: 1. \- To identify whether features of aberrant intermuscular coordination patterns can be used to predict motor impairment after stroke. 2. \- To test whether muscle synergies are malleable to a non-invasive EMG-guided exercise that induces changes in intermuscular coordination of upper extremity muscles after stroke.
CONDITIONS
Official Title
Increasing the Repertoire of Intermuscular Co-ordination Post Stroke Through EMG-Guided Human-Machine Interaction
Who Can Participate
Eligibility Criteria
You may qualify if you...
Inclusion criteria for aged matched healthy group
- Male or female whose age range between 40 and 75
- no known neurological injuries
Exclusion criteria for aged matched healthy group
- have an orthopedic disorder involving upper limbs;
- have a history of any neurologic disease;
- have any history of epilepsy of the potential participants and/or their family members;
- are unable to consent;
- are pregnant.
Inclusion criteria for stroke group
- male or female hemiparetic chronic stroke survivors;
- age ranging between 40-75 year;
- with single unilateral ischemic or hemorrhagic middle cerebral artery stroke;
- neurologically stable for >6 months;
- have an expectation that current medication will be maintained without changes for at least 3 months. Stable use of anti-spasticity medication (e.g., baclofen, diazepam, tizanidine) is accepted;
- without severe spasticity (Modified Ashworth (MA) <4);
- have not received botulinum toxin on the impaired arm within 3 months.
Exclusion criteria for stroke group
- have an orthopedic disorder involving upper limbs;
- cognitive impairment sufficient to interfere with informed consent or successful completion of the protocol (Montreal Cognitive Assessment (MoCA) score < 26);
- a history of another neurologic disease;
- anesthesia of joint position sense in upper limbs;
- are pregnant or have a chance that they might be (self-reported);
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Houston
Houston, Texas, United States, 77204
Actively Recruiting
Research Team
J
Jinsook Roh, PhD
CONTACT
M
Manuel A Portilla-Jiménez, MS, BME
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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