Chicago, ILNCT05849532Now EnrollingIRB Ready

Chronic Stroke Clinical Trial in Chicago, IL

Access cutting-edge chronic stroke treatment through this clinical trial at a research site in Chicago. Study-provided care at no cost to qualified participants.

Sponsored by University of Illinois at Chicago

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Expert Care in Chicago

Access chronic stroke specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related chronic stroke treatment provided free

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Check if you qualify for this chronic stroke clinical trial in Chicago, IL

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Why Participate?

  • No-Cost Study Care

  • Local to Chicago

    Convenient for IL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Chicago site if eligible
  4. 4Begin participation

About This Chronic Stroke Study in Chicago

This project will examine the feasibility, safety and effect of home-based functional electrical stimulation (FES) applied to different lower limb muscles in combination with task-specific training on gait, balance and mobility in adults with chronic stroke. 30 individuals with chronic stroke will first undergo initial screening and baseline walking, mobility, balance and strength assessments in the laboratory. After determining their eligibility for the study, they will undergo 12-weeks of home-based FES and task-specific training. Following the initial screening (week 1) and pre-intervention assessment (week 2), participants will be trained in the lab for 6 sessions (week 3-4) for a FES home program and then given a FES home kit (FES device and an android tablet). Participants will then undergo home-training for 2 weeks (week 5-6) followed by mid-training assessment (week 7). Again, participants will undergo 4-weeks of home training (week 8-11) and final assessment at the end of training (week 12). This project has the following specific aims: Aim 1: To investigate the feasibility, safety and efficacy of 12-weeks of home-based FES and task-specific training in adults with chronic stroke. Aim 2: To examine the effect of 12-weeks of home-based FES and task-specific training on mobility, gait and balance (anticipatory and reactive balance) in adults with chronic stroke.

Sponsor: University of Illinois at Chicago

Who Can Participate

Inclusion Criteria

Age group: 18-90 years.
Presence of unilateral hemiparesis.
Onset of stroke (\> 6 months).
Ability to walk independently with or without an assistive device for at least 300 ft.
Can understand and communicate in English and can verbalize discomfort or pain in English
Use of smartphone on a daily basis
Availability of internet/Wi-Fi at home

Exclusion Criteria

Body weight more than 250 lbs.
Heel bone density measurement using an ultrasound device. Individuals classified as osteoporotic (i.e., with a T-score \< -2) will be excluded.
Cognitive impairment (Montreal Cognitive assessment score \<26/30)
Verbal Aphasia (i.e \<71% score on Mississippi Aphasia Screening)
Severe depression (\> 15 points on geriatric depression scale)
Any neurological condition other than stroke.
Uncontrolled and/or untreated hypertension/hypotension, uncontrolled and/or untreated diabetes and any musculoskeletal, neuromuscular or systemic diagnosis .
Recent major surgery (\< 6 months) or hospitalization (\< 3 months).
Deep venous thrombosis.
Past or current history of any type of active cancer
Peripheral nerve injury or neuropathy in the affected limb with motor disability.
Uncontrolled high blood pressure/angina.
Skin condition not tolerant with FES therapy.
Past or current history of uncontrolled/controlled epilepsy or any other types of seizure disorders
Botox treatment within the last 5 months.
Pacemaker users. \-

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Chicago?

Yes, this clinical trial (NCT05849532) has an active research site in Chicago, IL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Chronic Stroke Treatment Options in Chicago, IL

If you're searching for chronic stroke treatment options in Chicago, IL, this clinical trial (NCT05849532) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Chicago research site is actively enrolling participants for this clinical trial. You'll receive care from experienced chronic stroke specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all chronic stroke clinical trials near you to find additional studies recruiting in your area.

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