Is NCT05762796 recruiting in Buffalo, NY?

Yes, NCT05762796 is currently recruiting participants at its Buffalo, NY location. This brain concussion clinical trial is actively enrolling qualified participants.

How do I join the brain concussion clinical trial in Buffalo?

To join this clinical trial in Buffalo, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this Buffalo clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Brain Concussion Clinical Trial in Buffalo, NY

About This Brain Concussion Study in Buffalo

Mild traumatic brain injury (mTBI) often causes persistent motor and cognitive deficits in children resulting in functional limitations. We are testing a brain stimulation method along with evaluating objective tools to help record and restore communication among affected brain areas, which will facilitate recovery in youth after mTBI.

Sponsor: State University of New York at Buffalo

Who Can Participate

Inclusion Criteria

age 10-15 years at enrollment

enrolled after 6 weeks of mTBI injury

exhibiting post-concussive symptoms (e.g., difficulty planning, sequencing, and executing a motor action)

Sustained an mTBI or concussion within the past 12 months

Parent and child proficient in English Healthy Controls Cohort: Inclusion Criteria:

10 to 15 years old

no concussion history

Parent and child proficient in English Experimental Cohort:

Exclusion Criteria

loss of consciousness \> 30 minutes

post-traumatic amnesia \> 24 hours

intracranial findings on clinical imaging

history of developmental delay

history of learning disability or ADHD

Sustained a lower limb or upper limb injury that has not healed

History of Seizures

Noticeable skin lesions/burns or any other severe skin problems at the site of the electrodes before the start of the stimulation.

Parent/guardian report metal implants anywhere in the head/ncek/body on the MRI screening form (see attached).

Parent/guardian report shrapnel/bullets in the body on the MRI screening form.

Parent/guardian report any electronic implant such as a cardiac pacemaker, cochlear implant, ventricular shunt, cardiac defibrillator, aneurysm clips, pacing wires, any implant held in place with a magnet, heart valve, or deep brain stimulator on the MRI screening form.

Parent/guardian report a craniotomy or any other surgery in the past 6 weeks on the MRI screening form.

Parent/guardian report being claustrophobic on the MRI screening form.

Parent/guardian report and provide orbit x-ray after the eye injury involving a metal that the subject is cleared as indicated on the MRI screening form.

Pregnant females as reported by parent/guardian on the pre-consent screening form. Pubertal/post-pubertal female participants14 and above will be provided a separate post-consent screening form at each MRI visit to ensure the female reports accurately without fear. Healthy Controls Cohort: Exclusion Criteria:

diagnosed with developmental delay

sustained a lower limb or upper limb injury that has not healed

history of Learning Disability and/or ADHD

Parent/guardian report metal implants anywhere in the head/ncek/body on the MRI screening form (see attached).

Parent/guardian report shrapnel/bullets in the body on the MRI screening form.

Parent/guardian report a craniotomy or any other surgery in the past 6 weeks on the MRI screening form.

Parent/guardian report being claustrophobic on the MRI screening form.

Parent/guardian report and provide orbit x-ray after the eye injury involving a metal that the subject is cleared as indicated on the MRI screening form.

Pregnant females as reported by parent/guardian on the pre-consent screening form. Post-pubertal females 14 and above will be provided a separate post-consent screening form at each MRI visit to ensure the female reports accurately without fear.

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 Buffalo?

Yes, this clinical trial (NCT05762796) has an active research site in Buffalo, NY 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 Buffalo, NY

If you're searching for brain concussion treatment options in Buffalo, NY, this clinical trial (NCT05762796) 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 Buffalo 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.

Brain Concussion Clinical Trial in Buffalo, NY

Expert Care in Buffalo

IRB Approved

No-Cost Care

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