NCT07006818Active, not recruiting
Impaired Interlimb Coordination During Locomotion in Individuals With Chronic Stroke: Contributors and Effect on Walking Function
Source: ClinicalTrials.gov · Last updated 21 Aug 2026
Brief summary (registry, in English)
Individuals with chronic stroke have long-term walking problems that limit community engagement and quality of life, lead to secondary disabilities, and increase healthcare costs and burden. These walking issues often persist despite rehabilitation. One novel target for stroke gait rehabilitation is interlimb coordination-the phase-dependent cyclical relation of the legs. Interlimb coordination is altered during walking after stroke, compromising walking stability, phase transitions, and responses to perturbation and contributing to motor compensation. It is unclear what neural pathways contribute to impaired interlimb coordination after stroke and what impact this has on walking-related outcomes. This proposal consists of two aims to address these issues, with the long-term goal of developing therapeutic interventions to improve interlimb coordination and walking after stroke. Aim 1 will identify which neural sources contribute to impaired interlimb coordination after stroke. During bilateral, cyclical recumbent stepping (analogue of walking), interlimb coordination will be assessed as relative leg phasing. During the task, transcranial magnetic stimulation and peripheral nerve stimulation will be applied to assess supraspinal, interhemispheric, spinal interneuronal, and sensory pathways. The relation of interlimb coordination with these outcomes will be assessed to determine potential contributors. Aim 2 will test the association between interlimb coordination and walking after stroke. Interlimb coordination will be quantified during split-belt treadmill walking, and associations with walking speed, endurance, mobility, independence, daily activity, quality of life, and community engagement will be tested. An additional exploratory aim will determine the effect of targeted neuromodulation on lower limb interlimb coordination. Electrical stimulation will be applied to three locations in a cross-over study: the primary motor cortex (supraspinal/interhemispheric), thoracolumbar spine (spinal interneuronal), and peripheral nerves (sensory).
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- First submitted
- 27 May 2025
- Start date
- 15 Sept 2025
- Primary completion date
- 30 Apr 2027
- Lead sponsor
- University of Illinois Chicago
- Diseases
- Stroke
- NCT number
- NCT07006818
What you commit to
- Study type: Interventional
- Planned participants: 50
- From 15 Sept 2025 to the primary completion date, 30 Apr 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous adverse reaction to TMS
- Concussion within the prior 6 months
- Metal implants in the head or face
Other illness
- Other neurological disorders
- Significant cognitive or communication impairment
- TMS exclusion criteria
- Implanted cardiac pacemaker
- History of seizures or epilepsy
- Use of medications that could increase risk of seizure
- Skin hypersensitivity at any sites of stimulation, including the scalp, thoracolumbar spine, and peripheral limbs
- History of contact dermatitis at any of the sites of stimulation
- History of allodynia and/or hyperalgesia
- Active skin infection
- Deep vein thrombosis
- Any other skin or scalp condition that could be aggravated by stimulation
Other
- Lesions affecting the brainstem or cerebellum
- Current botox treatments for the lower limb
- Skull abnormalities or fractures
- Unexplained, recurring headaches
- Current pregnancy
- PNS \& DCS exclusion criteria
- Skin lesions
- Implanted electronic, metallic, or highly conductive devices near site of stimulation that cannot be removed without permission from a health professional
Who the study is looking for
- Age: 25 - 90 years of age
- Monohemispheric stroke
- Chronic phase (\> 6 months post stroke)
- Ability to walk for at least 6 minutes at a self-selected comfortable speed
Age in the registry: 25 years to 90 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Illinois at Chicago Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.