Fayetteville, NCNCT05498038Now EnrollingIRB Ready

Brain Concussion Clinical Trial in Fayetteville, NC

Access cutting-edge brain concussion treatment through this clinical trial at a research site in Fayetteville. Study-provided care at no cost to qualified participants.

Sponsored by State University of New York at Buffalo

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Expert Care in Fayetteville

Access brain concussion specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related brain concussion treatment provided free

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Check if you qualify for this brain concussion clinical trial in Fayetteville, NC

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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 Fayetteville

    Convenient for NC 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 Fayetteville site if eligible
  4. 4Begin participation

About This Brain Concussion Study in Fayetteville

Our primary objective is to show that early, personalized aerobic exercise treatment safely improves concussion recovery, speeds RTD, and reduces persistent symptoms in CSM. Our secondary objectives include demonstrating the clinical utility of our March-in-place test and determining fundamental mechanisms for the effect of exercise rehabilitation on concussion recovery. We will conduct a prospective four-year multicenter mechanistic treatment (Phase 3) RCT in CSM of personalized sub-threshold aerobic exercise added to the PRA compared with the PRA alone. Non-concussed, age-matched SM will serve as a healthy control group (HC) for comparing CSM to normal physiology and to control for the effect of time and of aerobic exercise.

Sponsor: State University of New York at Buffalo

Who Can Participate

Inclusion Criteria

(Participants): For the CSM Group:
Active-duty service member
Aged 18-40 years
Injury occurred within 9 days of injury
Diagnosed with concussion by an experienced clinician using standard international criteria For the HC Group:
Active-duty service member

Exclusion Criteria

(Participants): For the CSM group:
Moderate or severe TBI as indicated by a GCS score \<13, lesion on CT/MRI, and/or focal neurologic sign consistent with intracerebral lesion
Injury involving loss of consciousness for \>30 minutes or post-traumatic amnesia \>24 hours
Inability to exercise because of lower-extremity orthopedic injury, clinically significant vestibular or visual dysfunction, or increased cardiac risk
Pre-existing conditions that prevent participation in active testing and/or rehabilitation
Active substance abuse/dependence
Unwillingness to perform intervention
Limited English proficiency
Confirmed pregnancy For the HC group:
Has lingering symptoms from a previous concussion or has recovered from a concussion less than 1-month ago
On a limited profile or "chit" for light duty
Active substance abuse/dependence
Unwilling to perform intervention
Limited English proficiency
Confirmed pregnancy Inclusion Criteria (Providers):
Active duty
Currently active clinician (MD, DO, PT, ATC, OT) involved in concussion management beyond initial emergent diagnosis
Willing to participate
Able to be contacted by telephone or Zoom Exclusion Criteria (Providers):
Not active duty
Not currently an active clinician (MD, DO, PT, ATC, OT) involved in concussion management
Only involved in concussion management at emergent timepoint
Unwilling to participate
Unable to be contacted by telephone or Zoom

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 Fayetteville?

Yes, this clinical trial (NCT05498038) has an active research site in Fayetteville, NC 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.

Brain Concussion Treatment Options in Fayetteville, NC

If you're searching for brain concussion treatment options in Fayetteville, NC, this clinical trial (NCT05498038) 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 Fayetteville research site is actively enrolling participants for this clinical trial. You'll receive care from experienced brain concussion 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 brain concussion clinical trials near you to find additional studies recruiting in your area.

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