Who is eligible for clinical trial NCT07214415?

Participants must meet the protocol's inclusion criteria for TBI Traumatic Brain Injury. The stated age range is 18 Years to 75 Years. Confirm all requirements with the study coordinator.

Does clinical trial NCT07214415 provide travel or cost reimbursement?

Check with the site coordinator at the participating facility for travel and lodging stipend availability, and for which routine-care costs are covered.

🏛️ Verified NIH Record • Updated 2025-10-06

Veterans' Cognitive Function, Mental Health, and Quality of Life After Hyperbaric Oxygen Therapy (NCT07214415)

Evaluating the Effects of Hyperbaric Oxygen Therapy on Cognitive Function, Mental Health, and Quality of Life in Veterans

🟢 Recruiting Phase2 💊 Investigational Drug / Biologic Sponsor: Summit Hyperbarics and Wellness

🩺 Plain-English Summary (8th-Grade Level)

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.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (9 items) and avoid the listed exclusions (30 items).

Location: Summit Hyperbarics and Wellness — Boise, Idaho

Age range: 18 Years to 75 Years

🧪 Interventions in This Study

Hyperbaric Oxygen Therapy (DRUG)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

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).

Usually NOT eligible if any of the following apply:

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

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (1 Sites)

Summit Hyperbarics and Wellness — Boise, Idaho

📞 Contact the Study Coordinator

Phone: (208) 813-9541

Email: tnickel@shwidaho.org

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

More studies in TBI Traumatic Brain Injury

DBS for Cognitive Deficits After Traumatic Brain Injury — Toronto, Ontario
Feasibility of SUPPORT-TBI — St Louis, Missouri

Explore by condition: All TBI Traumatic Brain Injury clinical trials

💡 How to Participate

Check the checklist above to see if you may qualify.
Contact the study coordinator using the phone/email above.
Ask about the visit schedule, what is covered at no cost, and any travel support.
Confirm with your own doctor before making a decision.

🏛️ View Official NIH Record ↗