Increasing the Repertoire of Intermuscular Co-ordination Post Stroke Through EMG-Guided Human-Machine Interaction
University of Houston · with Korea Advanced Institute of Science and Technology, The University of Texas Health Science Center, Houston · NCT06523335
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 40–75 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 74
- US sites recruiting
- 1
- Study start
- October 1, 2024
- Record last updated
- May 4, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purposes of this study include
- - To identify whether features of aberrant intermuscular coordination patterns can be used to predict motor impairment after stroke.
- - 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.
Being studied: Neuromuscular coordination-guided rehabilitative training; Force strengthening-guided rehabilitative training
Conditions: Stroke
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
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);
Recruiting US locations
University of Houston
Houston, TX 77204
Site contact: Jinsook Roh, PhD · 713-743-2578 · jroh@central.uh.edu
Study contacts (from the official record)
- Jinsook Roh, PhD · 7137432578 · jroh@Central.UH.EDU
- Manuel A Portilla-Jiménez, MS, BME · 3467194921 · maportillajimenez@uh.edu
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