Los Angeles, CANCT07485361Now EnrollingIRB Ready

Disorders of Consciousness Due to Severe Brain Injury Clinical Trial in Los Angeles, CA

Access cutting-edge disorders of consciousness due to severe brain injury treatment through this clinical trial at a research site in Los Angeles. Study-provided care at no cost to qualified participants.

Sponsored by University of California, Los Angeles

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Why Participate?

  • No-Cost Study Care

  • Local to Los Angeles

    Convenient for CA 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 Los Angeles site if eligible
  4. 4Begin participation

About This Disorders of Consciousness Due to Severe Brain Injury Study in Los Angeles

The goal of this observational study is to learn whether functional near-infrared spectroscopy (fNIRS) can measure brain activity in healthy adults and in people with disorders of consciousness (DoC) in the neuro-intensive care unit (Neuro-ICU). DoC include conditions such as coma and minimally conscious state that occur after severe brain injury. These conditions make it difficult to assess a person's level of awareness because many clinical tests rely on observable behaviors such as speaking or moving, which are commonly impaired after brain injury. The main questions the study aims to answer are: * Can fNIRS detect changes in brain activity in healthy adults when they receive sensory stimulation or perform mental tasks? * Can the same fNIRS protocol be used in patients with disorders of consciousness in the Neuro-ICU to measure brain responses and determine whether the method is feasible in this clinical setting? The investigators will first study healthy adult volunteers to establish baseline brain responses and determine which tasks produce the most reliable signals. The protocol will then be applied to patients with disorders of consciousness admitted to the Neuro-ICU. Participants will take part in a single research session lasting about 30 to 45 minutes while wearing the lightweight fNIRS headband that measures brain oxygen levels using near-infrared light. During the session, participants will: * Wear a non-invasive fNIRS headband placed on the forehead * Receive gentle sensory stimulation (for example, compression devices on the legs or hands) * Listen to sounds or spoken sentences * Perform guided mental tasks such as imagining walking through their home or imagining moving a limb The study does not test a treatment and will not change medical care. The goal is to determine whether fNIRS can safely and reliably measure brain activity at the bedside and provide preliminary information that may help guide future research on improving the assessment of consciousness after brain injury.

Sponsor: University of California, Los Angeles

Who Can Participate

Inclusion Criteria

Healthy Control Participants:
Age 18 years or older
Proficient in English language
Intact cognition
Montreal Cognitive Assessment (MoCA) score \> 26 DoC Patients:
Age 18 years or older
Proficient in English language
Surrogate decision maker available
Admission to the intensive care unit within 28 days
Documented Glasgow Coma Scale (GCS) score
Auditory Function subscale score ≥1 on the Coma Recovery Scale-Revised (CRS-R)

Exclusion Criteria

Healthy Control Participants:
Known baseline hearing impairment without available hearing aids
Neurological or psychiatric history DoC Patients:
Known baseline hearing impairment without available hearing aids
Inability to obtain informed consent
Extensive bilateral frontal injury on available imaging (CT/MRI)
Patients who have undergone craniectomy surgery
IV sedation in the past 24 hours
Absent auditory startle response (\<1 from Auditory Function subscale score of CRS-R)

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 Los Angeles?

Yes, this clinical trial (NCT07485361) has an active research site in Los Angeles, CA 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.

Disorders of Consciousness Due to Severe Brain Injury Treatment Options in Los Angeles, CA

If you're searching for disorders of consciousness due to severe brain injury treatment options in Los Angeles, CA, this clinical trial (NCT07485361) 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 Los Angeles research site is actively enrolling participants for this clinical trial. You'll receive care from experienced disorders of consciousness due to severe brain injury 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 disorders of consciousness due to severe brain injury clinical trials near you to find additional studies recruiting in your area.

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