Boise, IDNCT07214415Now EnrollingIRB Ready

TBI Traumatic Brain Injury Clinical Trial in Boise, ID

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

Sponsored by Summit Hyperbarics and Wellness

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Expert Care in Boise

Access tbi traumatic brain injury specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related tbi traumatic brain injury treatment provided free

Apply for This Boise Location

Check if you qualify for this tbi traumatic brain injury clinical trial in Boise, ID

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Boise

    Convenient for ID 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 Boise site if eligible
  4. 4Begin participation

About This TBI Traumatic Brain Injury Study in Boise

The purpose of this study is to evaluate how hyperbaric oxygen therapy (HBOT) may affect cognitive functioning, post-traumatic stress disorder (PTSD), depression, anxiety, and overall quality of life in veterans. 1. Does Hyperbaric Oxygen Therapy improve cognitive functioning, psychological well-being, and quality of life among veterans, as measured by pre-and post-treatment scores? 2. To what extent does Hyperbaric Oxygen Therapy improve cognitive functioning, psychological well-being, and qualify of life among veterans, after controlling for demographic characteristics.

Sponsor: Summit Hyperbarics and Wellness

Who Can Participate

Inclusion Criteria

At least 18 years of age.
Veteran status
Clinically diagnosed with a mTBI, PTSD, Anxiety, or Depression disorder by meeting the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, and by a qualified and trained professional.
The subject is willing and able to read, understand, and sign an informed consent. Additionally, the subject has clear consciousness and the ability to express self-feelings independently.
Exposed to at least one trauma-focused therapy or evidence-based psychotherapeutic treatment, such as prolonged exposure therapy, EMDR, or CBT, to name a few.
Completed cognitive and psychological measurements.
Clinical diagnoses cause significant impairment in social or occupational functioning or some other functional capacity.
Sexually active female participants of childbearing potential and sexually active male participants with female partners of childbearing potential must agree to use an acceptable method of contraception for the duration of the study and for 30 days following the final HBOT session.
Stability on any current psychoactive medications (antidepressants, anti-anxiety medications, antipsychotics, stimulants, and mood stabilizers).

Exclusion Criteria

Untreated pneumothorax
History of spontaneous pneumothorax
Severe sinus infection
Upper respiratory infection
Asymptomatic pulmonary lesions on chest x-ray
Uncontrollable high fever (greater than 39C)
History of chest or ear surgery
Congenital spherocytosis
Any anemia or blood disorder
Any convulsive disorder
History of optic neuritis or sudden blindness
Middle ear infection
Diabetes mellitus (insulin therapy)
The subject is pregnant or lactating
Nicotine use/substance use/addiction
Acute Hypoglycemia
Diagnosed Chronic Obstructive Pulmonary Disease (COPD) and Emphysema
Presenting with symptoms of cough, congestion, vomiting, diarrhea, or open wounds.
Active malignancy
Current manic, delusional, or psychotic episodes
Serious/current suicidal ideations
Severe or unstable physical disorders or major cognitive deficits
Inability to attend scheduled clinic visits or comply with study protocols.
Treated with HBOT for any reason prior to study enrollment.
Non-English speakers
History of retinal repair, including laser photocoagulation or retinal detachment surgery.
History of middle ear surgery, including tympanoplasty, mastoidectomy, or pressure equalization tube placement.
Age greater than 75 years.
Use of any of the following medications during the study period: Anti-metabolites (e.g., methotrexate, azathioprine); Chemotherapuetic agents (e.g., cyclophosphamide, cisplatin); Mafenide acetate e.g., Sulfamylon); Disulfiram (e.g, Antabuse); Peripheral vasodilators known to interact with oxygen exposure (e.g., nitroglycerin); and Antibacterial drugs with known HBOT interaction risks.

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 Boise?

Yes, this clinical trial (NCT07214415) has an active research site in Boise, ID 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.

TBI Traumatic Brain Injury Treatment Options in Boise, ID

If you're searching for tbi traumatic brain injury treatment options in Boise, ID, this clinical trial (NCT07214415) 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 Boise research site is actively enrolling participants for this clinical trial. You'll receive care from experienced tbi traumatic 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 tbi traumatic brain injury clinical trials near you to find additional studies recruiting in your area.

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