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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

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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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Increasing the Repertoire of Intermuscular Co-ordination Post… (NCT06523335) | Bored Studies