Stony Brook, NYNCT07560631Now EnrollingIRB Ready

Traumatic Brain Injury (TBI) Patients Clinical Trial in Stony Brook, NY

Access cutting-edge traumatic brain injury (tbi) patients treatment through this clinical trial at a research site in Stony Brook. Study-provided care at no cost to qualified participants.

Sponsored by Stony Brook University

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Expert Care in Stony Brook

Access traumatic brain injury (tbi) patients specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related traumatic brain injury (tbi) patients treatment provided free

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Check if you qualify for this traumatic brain injury (tbi) patients clinical trial in Stony Brook, NY

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Why Participate?

  • No-Cost Study Care

  • Local to Stony Brook

    Convenient for NY 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 Stony Brook site if eligible
  4. 4Begin participation

About This Traumatic Brain Injury (TBI) Patients Study in Stony Brook

Objective: This prospective interventional study introduces "SeeMe," an automated, high-resolution computer vision platform designed to objectively quantify microscopic, auditory command-evoked movements in patients with Traumatic Brain Injury (TBI). Current clinical assessments, such as the Glasgow Coma Scale (GCS) and Coma Recovery Scale-Revised (CRS-R), rely on subjective human observation and often fail to detect low-amplitude motor responses, potentially misclassifying up to 25% of patients as unresponsive. Methodology: SeeMe utilizes vector analysis, cross-correlation, and deep neural networks (DNNs) to track individual facial pores and hand movements with sub-millimeter precision (0.5 mm) and high temporal resolution (0.03s). The study will enroll a cohort of 60-80 TBI patients, alongside healthy controls and pharmacologically paralyzed subjects, to validate SeeMe's sensitivity and specificity. Primary Goals: 1. Validation: Compare SeeMe's detection of voluntary motor recovery against gold-standard clinical examinations (CRS-R). 2. Synchronization: Simultaneously record and time-lock electroencephalography (EEG) and electrocorticography (ECoG) with SeeMe-detected movements. 3. Biomarker Identification: Characterize neural signatures (specifically Beta-band oscillations) associated with the return of voluntary behavior. Impact: By providing a real-time, objective measure of motor intention and execution, SeeMe aims to identify "Cognitive-Motor Dissociation" (CMD) earlier than current methods, facilitating more accurate prognostications and laying the framework for future closed-loop neuromodulation (e.g., Vagus Nerve Stimulation) to accelerate TBI recovery.

Sponsor: Stony Brook University

Who Can Participate

Inclusion Criteria

Adults (22+) with a history of acute traumatic brain injury
Documented loss of consciousness with a Glasgow Coma Scale (GCS) score less than or equal to 8 upon hospitalization
Clinically stable as determined by the primary neurosurgery or ICU team
Intact auditory pathways as confirmed by BAERs
Family consent for study participation

Exclusion Criteria

Hearing Impairment confirmed via absence of Brainstem Auditory Evoked Responses (BAERs) that would prevent the patient from hearing the auditory commands
No legal authorized representative (LAR) available to provide informed consent for the patients in a comatose state
Any other medical condition that, in the judgment of the investigator, makes participation in the study unsafe.
Pregnant women
Any previous history of traumatic brain injury
Any neurodegenerative disease such as dementia Group 2: Healthy Control Cohort Inclusion Criteria:
Adults 22+ with no history of neurological or psychiatric disorders
Normal baseline neurological examination
Intact auditory pathways
Ability to provide informed consent
Ability to follow simple auditory commands in English Exclusion Criteria:
Hearing Impairment that would prevent the participant from hearing the auditory commands
Any previous history of severe traumatic brain injury (TBI)
Any neurodegenerative disease (e.g., dementia)
Any motor impairment (e.g., facial palsy, carpal tunnel syndrome) that would interfere with facial or hand movement tracking
Any other medical condition that, in the judgment of the investigator, makes participation in the study unsafe
Pregnant women Group 3: Sedated/Anesthetized Cohort Inclusion Criteria:
Adults (22+) undergoing elective spine surgery
Requirement of general anesthesia and pharmacological paralysis (neuromuscular blockade) as part of the standard surgical procedure
Clinically stable for study procedures as determined by the anesthesia and surgical teams.
Intact auditory pathways
Ability to provide informed pre-operative consent Exclusion Criteria:
Hearing Impairment that would prevent the patient from hearing the auditory commands
Any previous history of severe traumatic brain injury
Any neurodegenerative disease such as dementia
Significant baseline facial or hand motor deficits prior to the administration of anesthesia
Any other medical condition that, in the judgment of the investigator, makes participation in the study unsafe
Pregnant women

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 Stony Brook?

Yes, this clinical trial (NCT07560631) has an active research site in Stony Brook, 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.

Traumatic Brain Injury (TBI) Patients Treatment Options in Stony Brook, NY

If you're searching for traumatic brain injury (tbi) patients treatment options in Stony Brook, NY, this clinical trial (NCT07560631) 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 Stony Brook research site is actively enrolling participants for this clinical trial. You'll receive care from experienced traumatic brain injury (tbi) patients 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 traumatic brain injury (tbi) patients clinical trials near you to find additional studies recruiting in your area.

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