Wilmington, DENCT07574632Now EnrollingIRB Ready

Idiopathic Scoliosis Clinical Trial in Wilmington, DE

Access cutting-edge idiopathic scoliosis treatment through this clinical trial at a research site in Wilmington. Study-provided care at no cost to qualified participants.

Sponsored by Thinks Works, PBC

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Expert Care in Wilmington

Access idiopathic scoliosis specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related idiopathic scoliosis treatment provided free

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Check if you qualify for this idiopathic scoliosis clinical trial in Wilmington, DE

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

Why Participate?

  • No-Cost Study Care

  • Local to Wilmington

    Convenient for DE 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 Wilmington site if eligible
  4. 4Begin participation

About This Idiopathic Scoliosis Study in Wilmington

The goal of this clinical trial is to learn if the RESILIENT Scoliosis Brace System works to treat children with idiopathic scoliosis. It will also learn about the safety, comfort, and usability of the brace. The main questions it aims to answer are: * Can the RESILIENT brace prevent the spinal curve from progressing beyond 35 degrees during growth? * How much does the brace correct the curve when it is first worn (in-brace correction)? * How well do participants follow the prescribed brace wear time and force levels? * How does wearing the brace affect quality of life and daily activities? Researchers will study a single group of participants using the RESILIENT brace and evaluate outcomes over time using standard clinical assessments, including X-rays and patient-reported questionnaires. Participants will: * Be fitted with the RESILIENT brace and instructed on how to use it * Wear the brace daily according to physician recommendations throughout their growth period * Attend clinic visits at approximately 4-6 weeks after starting treatment and then about every 6 months for follow-up evaluations * Undergo standard-of-care spine X-rays to monitor curve progression * Complete questionnaires about their quality of life and experience with the brace * Have brace wear time and applied forces monitored using sensors embedded in the device Participants will be followed from the start of brace treatment until they are done growing and have completed treatment.

Sponsor: Thinks Works, PBC

Who Can Participate

Inclusion Criteria

Diagnosis of Idiopathic Scoliosis (IS)
Age of 9 - 16 years when brace treatment is prescribed
Primary right apex main thoracic scoliosis curve with an apex of T6 or lower
Cobb angle, as measured on a standing PA spine x-ray, 20 degrees or larger and 30 degrees or less, obtained no more than 6 weeks prior to trial enrollment.
Sanders Skeletal Maturity Score of 1-5
No prior brace treatment or surgery for scoliosis
Patient \& guardian select the RESILIENT brace for treatment
The guardian must confirm that there is cellular connectivity at the place(s) where the patient lives

Exclusion Criteria

Scoliosis other than idiopathic scoliosis: e.g. Neuromuscular, Congenital, or Syndrome Related
Age less than 9 years or older than 16 years
Sanders Skeletal Maturity Score of 6 or greater
Primary Left apex thoracic scoliosis
Primary lumbar scoliosis
Primary Right Thoracic curve with an apex above T6
Inability to remove and apply the brace independently
Inability to respond to written and verbal questions
Patient \& Guardian select traditional TLSO for treatment
Guardian confirms there is no cellular connectivity at the place(s) where the patient lives

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 Wilmington?

Yes, this clinical trial (NCT07574632) has an active research site in Wilmington, DE 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.

Idiopathic Scoliosis Treatment Options in Wilmington, DE

If you're searching for idiopathic scoliosis treatment options in Wilmington, DE, this clinical trial (NCT07574632) 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 Wilmington research site is actively enrolling participants for this clinical trial. You'll receive care from experienced idiopathic scoliosis 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 idiopathic scoliosis clinical trials near you to find additional studies recruiting in your area.

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