Long-Term Outcomes Following HBOT

Part of paid clinical trials in Boise, Idaho.

Sponsor
Summit Hyperbarics and Wellness
Study ID
NCT07732374
Phase
PHASE2
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Hyperbaric Oxygen Therapy (HBOT) — DRUG
    Hyperbaric Oxygen Therapy (HBOT): Participants will receive 100% medical oxygen (USP) administered under hyperbaric conditions at 2.0 atmospheres absolute (ATA) for 60 minutes with a scheduled air break over 40 treatment sessions.

Study Details

This study is designed to better understand the long-term effects of hyperbaric oxygen therapy (HBOT). Our goal is to determine whether improvements after treatment are maintained over time and whether additional benefits appear months after treatment has ended. We will evaluate changes in cognitive function, mental health, and daily functioning to help strengthen the scientific evidence supporting the use of HBOT and guide future treatment recommendations.

Key Dates

First listed
Jul 28, 2026
Start date
Jun 18, 2026
Status verified
Jun 2026
Primary completion
Jun 18, 2027
Completion
Jun 18, 2027

Study Design

Enrollment
35 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: HBOT Follow-Up Cohort
    Veterans who previously completed a standardized Hyperbaric Oxygen Therapy (HBOT) treatment protocol and undergo follow-up assessments approximately 12 weeks after their final treatment session to evaluate the long-term durability of cognitive, psychological, and quality-of-life outcomes.

Primary Outcome Measure

NeuroTrax [ Time Frame: Baseline (post-HBOT completion) and 12 weeks after the final HBOT session ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Summit Hyperbarics and WellnessBoiseIdaho83716
Troy Nickel, PhD
208-813-9541
Steven Wyman, MD (PRINCIPAL_INVESTIGATOR)

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