Improving arm control after stroke
Official title: Intermuscular Coordination as a Novel Clinical Target for Stroke Neurorehabilitation
Run by University of Houston · NCT06523335 · Data updated 2026-11-12
This study is testing a new exercise program to help stroke survivors improve their arm movement by using special technology to guide their workouts.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 40 Years to 75 Years |
| Sex | All |
| Enrollment | 74 (estimated) |
| Sponsor | University of Houston Academic / other |
| Locations | 1 site (Houston, Texas) |
| Status | Recruiting |
| Started | October 1, 2024 |
| Main results expected | September 1, 2029 |
| Study ends | September 1, 2029 |
| Registry record updated | May 4, 2026 |
| Trial ID | NCT06523335 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are chronic hemiparetic stroke survivors aged 40-75 who are neurologically stable and have not received certain recent treatments.
✕Probably not a fit
Patients with severe spasticity or those who have received botulinum toxin treatment on the impaired arm within the last three months may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to identify patterns of intermuscular coordination that can predict motor impairment in stroke survivors and to test a non-invasive electromyogram-guided exercise designed to improve upper extremity function. It will involve both healthy adults and stroke survivors, with participants undergoing assessments and targeted rehabilitation exercises over several weeks. The study seeks to normalize abnormal muscle coordination patterns to enhance motor recovery post-stroke.
Why it matters
Potential benefit: If successful, this approach could significantly improve arm function and quality of life for stroke survivors.
How similar studies have gone: Other studies have shown promise in using electromyogram-guided rehabilitation techniques, indicating potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion 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);
Where it's running
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University of Houston
Houston, Texas, United States Recruiting
Study contacts
- Principal investigator: Jinsook Roh, PhD — University of Houston
- Study coordinator: Jinsook Roh, PhD
- Email: jroh@Central.UH.EDU
- Phone: 7137432578
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Deep phenotyping to explore recovery in young adults after stroke
This project will test whether a detailed health and sample-collection approach (deep phenotyping) is practical and acceptable for people aged 18–55 who have had a stroke.
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Stem cell therapy for chronic stroke recovery
This study is testing whether using a patient's own stem cells can help people with long-term stroke recovery feel better and improve their daily functioning.
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AI-based tools to help diagnose, treat and predict stroke outcomes across multiple hospitals
This study tests AI-powered tools on real-world stroke patients to see if they can improve pre-hospital triage, diagnosis, and outcome prediction while data stay securely within each hospital.
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Web-based therapy using action observation and mirror therapy for arm weakness after stroke
This trial tests whether a mobile telerehabilitation app delivering action observation therapy (AOT) alone or combined AOT with mirror therapy (AOT-MT) can improve upper limb function in people with subacute stroke.
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Remote Ischaemic Conditioning for Fatigue After Stroke 2
Aat least 12 weeks after stroke, adults with post-stroke fatigue will try a simple hand-arm cuff treatment at home to see if it helps reduce fatigue.
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Dual-task balance training plus computer-based cognitive training after stroke
In adults who recently had a stroke, the study tests whether adding computerized cognitive exercises to balance training improves balance and other recovery outcomes.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.