Neuropsychiatric
Post-Traumatic Stress Disorder (PTSD)
Post-traumatic stress disorder is an increasingly studied HBOT target. A sham-controlled randomised trial in combat veterans reported substantial reductions in PTSD severity alongside measurable changes in brain connectivity, with early independent corroboration. The randomised evidence comes largely from one research group; HBOT for PTSD remains investigational and is not FDA-approved.
Evidence summary
Post-traumatic stress disorder (PTSD) is a trauma- and stressor-related disorder marked by intrusive memories, avoidance, hyperarousal, and altered mood and cognition, with documented changes in brain activity and white-matter integrity.
A specific HBOT protocol has been studied as a means of inducing neuroplasticity in established, often treatment-resistant PTSD; rather than acting pharmacologically, it is proposed to drive neuroplasticity through the hyperoxic-hypoxic paradox, accompanied in trials by improved resting-state functional connectivity across the default-mode, central-executive and salience networks (2024) and increased white-matter fractional anisotropy in fronto-limbic tracts, the genu of the corpus callosum and the fornix on diffusion tensor imaging (2022).
A randomised, sham-controlled trial in 56 combat veterans (60 sessions, 90 minutes, 100% O₂ at 2 ATA) found CAPS-5 scores fell from 42.6 to 25.8 with HBOT while the sham group did not improve; an earlier randomised controlled trial in treatment-resistant PTSD showed concordant symptom and neuroimaging improvements; a 2026 systematic review and meta-analysis pooled two sham-controlled PTSD RCTs and reported a large effect while cautioning that studies are small and preliminary; and a 2026 prospective observational cohort of 50 US veterans reported reductions sustained to six months.
The investigational protocol as studied — not a clinical recommendation — comprised 60 daily sessions of 90 minutes, 100% oxygen at 2 ATA, with intermittent air breaks.
The randomised evidence originates substantially from a single research group (Sagol Center / Shamir Medical Center) — the same lineage as the Long COVID and Fibromyalgia entries — though, unlike those, there is now early independent corroboration (a US observational cohort and a meta-analysis by an unaffiliated group). Sample sizes remain small and larger multicentre randomised trials are needed. HBOT for PTSD remains investigational and is not FDA-approved.
Treatment protocol
Protocol
Pressure
2 ATA
Duration
90 min
Sessions
60
Frequency
Daily, with air breaks
Evidence basis: Doenyas-Barak et al., 2024 (RCT)
References:
See full citations on the references page.
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