Decoding the Brain's walking blueprint after stroke
NCT ID NCT04805866
First seen Jul 14, 2026 · Last updated Jul 15, 2026 · Updated 1 time
Summary
This study investigates how the brain coordinates muscle activity during walking rehabilitation in people recovering from a stroke. Researchers use high-density electromyography (HD-EMG) to track neural synergies—groups of muscles that receive common signals from the brain—over the course of inpatient therapy. The goal is to understand how these patterns change and relate to walking improvements, which could inform future rehabilitation strategies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this research could lead to more personalized and effective gait rehabilitation programs for stroke survivors.
- What could go wrong
- This is an observational study with a small sample size, so findings may not apply to all stroke patients. The technology is also experimental and may not translate directly into clinical practice.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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36 people
The number who actually took part.
- Started
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Jun 2021
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Individuals poststroke that are inpatients at Shirley Ryan AbilityLab and Healthy individuals as age-matched controls
- Ages
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18 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Healthy participants: Inclusion Criteria: * Age 18-85 years old * Ambulatory with or without an assistive device * Ability to stand unassisted for at least 15 min * Informed consent provided by participant * English speaking Exclusion Criteria: * Inability to communicate with researchers * Lower extremity joint pain, contractures * Major sensory deficits, or cardiovascular or respiratory symptoms contraindicative of walking * History or evidence of orthopedic, muscular, or physical disability * Taking current medications that may affect balance * History or evidence of vestibular, auditory, or proprioceptive impairment * History or indication of orthostatic hypotension * History of any neurological disease * Open wounds on surfaces in contact with HD-EMG electrodes * Concurrent participation in other lower limb research studies that according to the PI is likely to affect study outcome or confound results * Pregnancy Patients: Inclusion Criteria: * Age 18-85 years old * Unilateral, supratentorial ischemic or hemorrhagic stroke within the past six months * Medical clearance from primary medical team (signed Medical Clearance form) * Unassisted sitting balance at edge of mat or hospital bed ≥ 30 seconds * Baseline Visible muscle contraction in hip flexors, knee extensors, and ankle dorsiflexors ( ≥1 MMT) or manual resistance against one muscle group (\>3 MMT) * Adequate cognitive function as determined by the NIH scale: score ≤1 on question 1b and score =0 on question 1c * Informed consent provided by participant or POA * English speaking Exclusion Criteria: * Severe aphasia limiting ability to express needs or discomfort verbally or nonverbally * Severe behavioral neglect * History of prior stroke * Concurrent neurologic condition (i.e PD, TBI, MS, etc.) * History of peripheral nerve injury * Joint contracture or significant spasticity in the lower limbs (Modified Ashworth Scale ≥3) * Severe knee, hip, or ankle osteoarthritis * Severe osteoporosis as indicated by physician medical clearance * Open wounds on surfaces in contact with HD-EMG electrodes * Unstable spine or unhealed fractures * Weight bearing precautions * Unresolved deep vein thrombosis (DVT) * Concurrent participation in other lower limb research studies that according to the PI is likely to affect study outcome or confound results * Pregnancy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Shirley Ryan AbilityLab
Chicago, Illinois, 60611, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Stroke rehabilitation with innovative extended reality (STRIVE): a feasibility study in clinical practice
- Health, functioning, work, and experiences of social and health services of persons with stroke
- Insights into impaired arm motor control on bilateral and unilateral functional activities after injury: a kinematic study
- Emergency stroke unit for acute cerebrovascular events: a prospective, single-arm trial with a historical control group
- Effects of transcranial direct current stimulation and pelvic proprioceptive neuromuscular facilitation on trunk control, balance and functional mobility in stroke patients
- Correlation of visual and motor deficits in stroke patients