Chicago, ILNCT05424172Now EnrollingIRB Ready

Spinal Cord Injuries Clinical Trial in Chicago, IL

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

Sponsored by Shirley Ryan AbilityLab

Quick Self-Assessment

See if you qualify for this Chicago location

Preparing your pre-screening questions…

Expert Care in Chicago

Access spinal cord injuries specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related spinal cord injuries treatment provided free

Apply for This Chicago Location

Check if you qualify for this spinal cord injuries clinical trial in Chicago, IL

Secure & Confidential

Your information is protected and will only be shared with the research team.

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 Spinal Cord Injuries Study in Chicago

The goal of this research is to increase physical activity among individuals with a spinal cord injury (SCI) through a customized, interactive smartphone-based health app and e-coaching using three phases: (1) leading focus groups of potential app users and clinicians to gain information regarding health apps preferences for optimal consumer use, (2) conducting a usability study of the customized app to determine the quality and implement further changes for optimization, and (3) conducting a sequential multiple assignment randomized trial (SMART) to determine the most effective adaptive intervention to improve exercise adherence. A SMART trial will be used to determine when and how to adapt dosage, timing, and delivery to increase adherence and address low-response behaviors. In Stage-I, the investigators will compare outcomes among participants using a generic, non-interactive exercise app (Group 1) to a customized, interactive app that can gain information through frequent Ecological Momentary Assessments (EMA) that will be used to modify each participant's exercise programs (Group 2). After 12 weeks, participants who are not meeting the exercise guidelines at least 50% of the time will also be asked to participate in motivational interviewing-based e-coaching either two or four times per month in addition to their originally assigned intervention (Stage-II). By completing these three phases, this project addresses deficiencies in exercise levels and compliance by implementing an individualized exercise prescription, an adaptive intervention for low responders, a way to address barriers to exercise, and a free smartphone app for broad implementation.

Sponsor: Shirley Ryan AbilityLab

Who Can Participate

Inclusion Criteria

Individual with diagnosis of SCI, formal or informal caregiver of an individual with an SCI, or clinician that regularly sees individuals with SCI
18-80 years of age
English-speaking
Willing to download the study apps

Exclusion Criteria

Severe visual or cognitive problems that would affect the ability to complete the study
Does not own, or is unable to use a smartphone Inclusion Criteria: Phase 2 and 3
Individual with diagnosis of SCI, complete (only paraplegia) or incomplete, cervical C3- C4 and below
18-80 years of age
English-speaking
Use a wheelchair as primary means of mobility or walk with or without assistive equipment
At least 1-year post-SCI
Not adhering to SCI-specific exercise guidelines as ascertained by self-report or during structured phone interview
Interested in increasing exercise levels
Ownership of a smartphone that can be used for the study and has a data plan
Willing to successfully download and learn to use the study apps
Able and willing to give written consent and comply with study procedures, including multiple in person follow-up visits Exclusion Criteria: Phase 2 and 3
Trauma or surgery in the past three months
An active stage 3 or 4 pressure ulcer
Medically unstable to perform the home-based exercise as determined by Dr. Chen and his team, the evaluating physical therapist, or the participants' primary care physician.
Unable to use at least one set of extremities to exercise
Enrolled in a structured exercise program over the past three months
Severe visual or cognitive problems that would affect the ability to complete the study
Does not own, or is unable to use a smartphone

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 (NCT05424172) 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.

Spinal Cord Injuries Treatment Options in Chicago, IL

If you're searching for spinal cord injuries treatment options in Chicago, IL, this clinical trial (NCT05424172) 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 spinal cord injuries 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.

Ready to Join in Chicago?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Chicago, IL