Can Hyperbaric Oxygen Therapy Improve Fitness in Middle-Aged Athletes?
Yes. This double-blind randomized controlled trial found 40 sessions of HBOT significantly improved VO2max (effect size 0.99), anaerobic threshold (effect size 0.84), mitochondrial respiratory capacity (effect size 1.09), and increased mitochondrial mass by 17% compared to -9% in controls. This is the first blinded RCT to demonstrate HBOT enhances athletic performance.
Previous studies suggested hyperbaric oxygen might enhance performance, but none used proper placebo controls. This Israeli study used rigorous double-blinding, muscle biopsies to measure mitochondrial changes, and cardiopulmonary exercise testing to assess real-world performance.
What the Data Show
Study Design:
- Double-blind, randomized, placebo-controlled trial
- 37 athletes enrolled, 31 completed (16 HBOT, 15 sham)
- Age: 40-50 years (middle-aged master athletes)
- Training level: Aerobic sports ≥4 times/week at moderate-high performance
- Protocol: 40 sessions, 5 per week, over 2 months
- Registered: ClinicalTrials.gov NCT03524989
HBOT Protocol:
- 100% oxygen at 2 ATA (absolute atmospheres)
- 60 minutes per session
- Compression/decompression: 1 m/min
SHAM Placebo Protocol:
- 21% oxygen (room air) at 1.02 ATA
- Brief compression to 1.2 ATA for blinding
- Same 60-minute duration
Blinding Success: 63% of HBOT group thought they received sham; 53% of sham group thought they received sham (p=0.60, no difference)
Cardiopulmonary Exercise Test Results:
| Measure | HBOT Change | Sham | Effect Size | P-value |
|---|---|---|---|---|
| VO2max (ml/min) | 2834→2956 | No change | 0.989 | 0.010 |
| VO2/kg | Increased | No change | Similar | Significant |
| VO2 at AT (ml/min) | 1197→1327 | No change | 0.837 | 0.026 |
| Maximal power | Increased | No change | 0.808 | 0.03 |
| Breathing reserve | Decreased | No change | -0.91 | 0.016 |
Mitochondrial Respiration (Muscle Biopsies, n=22):
| Measure | HBOT vs SHAM | Effect Size | P-value |
|---|---|---|---|
| Max OxPhos capacity | Significant increase | 1.085 | 0.04 |
| Max uncoupled capacity | Significant increase | 0.956 | 0.02 |
| Complex I function | Significant increase | 1.120 | 0.01 |
| Complex II uncoupled | No change | - | NS |
| Proton leak | No change | - | NS |
Mitochondrial Mass (Muscle Biopsies, n=12):
| Marker | HBOT Change | SHAM Change | P-value |
|---|---|---|---|
| MTG (mass marker) | +17.12% | -8.54% | 0.0002 |
| PGC1alpha (biogenesis) | Increased | - | NS (0.699) |
| OPA1 (fusion) | Increased | - | NS (0.12) |
| MNF1+2 (fusion) | Increased | - | NS (0.09) |
No significant changes in:
- Body composition
- Pulmonary function
- Range of motion
- Vertical jump
- Agility tests
Dr. Kumar’s Take
This study is a landmark because it’s the first properly controlled trial showing HBOT improves athletic performance. The double-blinding worked (63% of HBOT subjects thought they got placebo), so we can trust the results aren’t due to expectation effects.
The effect sizes are large. A 0.99 effect size for VO2max means the average HBOT subject improved more than 84% of the control group. For context, that’s comparable to what you’d see from months of dedicated training programs.
What makes this study exceptional is the muscle biopsy data. The researchers didn’t just measure performance - they looked inside muscle cells and found more mitochondria with better respiratory function. The 17% increase in mitochondrial mass versus a 9% decrease in controls (p=0.0002) provides a clear biological explanation for the performance gains.
The mechanism appears to be what the researchers call the “hyperoxic-hypoxic paradox” - intermittent high oxygen exposure triggers the same HIF1α pathway that hypoxic training does, but without the downsides of training with insufficient oxygen.
The Hyperoxic-Hypoxic Paradox
Traditional high-altitude or hypoxic training stimulates mitochondrial adaptations through the HIF1α transcription factor. However, continuous hypoxia actually reduces mitochondrial number and inhibits respiration because oxygen remains insufficient.
Intermittent HBOT works differently:
- Relative oxygen changes (rather than constant hypoxia) trigger HIF1α
- Oxygen supplies remain normal or super-normal
- Mitochondrial biogenesis occurs without the hypoxic limitation
- Both mitochondrial number and quality improve
This explains why single HBOT sessions don’t help (no cumulative adaptation) while 40 sessions produce significant changes.
Why These Results Matter
For Master Athletes: Middle-aged athletes face declining mitochondrial function, which limits VO2max and endurance. This protocol offers a potential way to reverse some age-related decline.
For Exercise Science: The study provides mechanistic evidence that HBOT works at the cellular level, not just through temporary oxygen availability.
For HBOT Research: This demonstrates that proper placebo controls are possible in HBOT research, setting a new standard for the field.
Study Limitations
Sample Size:
- 31 athletes completed the study
- Only 22 had usable muscle biopsies for respiration
- Only 12 had biopsies for mass markers
- Despite small numbers, large effect sizes produced significant results
Baseline Differences:
- Significant differences in mitochondrial respiration at baseline
- Mitigated using ANCOVA analysis
Protocol Questions:
- Is 40 sessions optimal, or would fewer work?
- How long do benefits last?
- Would different pressures or durations produce different results?
Generalizability:
- Only studied athletes aged 40-50
- All maintained active training programs
- Results may differ in younger athletes or sedentary individuals
Safety and Side Effects
HBOT Group:
- 2 subjects developed upper respiratory viral infections
- Attributed to season, not treatment
SHAM Group:
- 2 subjects developed pneumonia
Biopsy-Related:
- 1 gluteal subcutaneous hematoma, treated conservatively
No HBOT-specific adverse events: No barotrauma, no oxygen toxicity
Practical Takeaways
- 40 HBOT sessions significantly improved VO2max in master athletes (effect size 0.99)
- Benefits appear mediated by improved mitochondrial function and mass
- Single sessions unlikely to help based on previous research
- Proper blinding confirmed this isn’t a placebo effect
- Protocol requires substantial time commitment (40 hours over 2 months)
- Works through “hyperoxic-hypoxic paradox” - oxygen fluctuations trigger adaptation
- No body composition or basic pulmonary function changes observed
- Safety profile was good in this controlled setting
Related Studies and Research
- Effects of Hyperoxia on Sea Level Exercise Performance
- Influence of Hyperoxic-Supplemented High-Intensity Interval Training
- HBOT for Exercise Performance and Recovery: Meta-Analysis
- Impact of Aging on Mitochondrial Respiration in Various Organs
FAQs
How many HBOT sessions are needed for athletic benefits?
This study used 40 one-hour sessions over 2 months. Previous studies using single sessions found no lasting benefits. The repeated intermittent exposures appear necessary to trigger mitochondrial adaptations. Whether fewer sessions could work remains unknown - this needs further study.
Is this different from breathing oxygen during exercise?
Yes, fundamentally different. Hyperbaric oxygen therapy delivers oxygen at 2 atmospheres of pressure in a sealed chamber, which dissolves far more oxygen into blood and tissues than normal breathing. More importantly, the intermittent nature of HBOT sessions (oxygen fluctuations rather than constant exposure) appears key to triggering cellular adaptations.
Why did mitochondrial mass increase but not the biogenesis marker (PGC1alpha)?
The muscle biopsies were taken 1-2 weeks after the last session. Active biogenesis (formation of new mitochondria) may have completed by then, leaving increased mass as the result. The non-significant increases in PGC1alpha, OPA1, and MNF1+2 all trended upward, suggesting the small sample size (n=12) limited statistical power.
Would this help younger athletes?
Unknown. This study only included athletes aged 40-50. Younger athletes typically have better baseline mitochondrial function. The effects might be smaller, larger, or similar - it hasn’t been studied. Middle-aged athletes may have more “room for improvement” in mitochondrial function.
Are there risks to repeated HBOT exposure?
This study reported no HBOT-specific adverse events (no ear barotrauma, no oxygen toxicity). However, HBOT does carry theoretical risks including ear pressure issues, rarely seizures from oxygen toxicity, and requires medical supervision. The controlled setting with professional operators likely contributed to the safety profile.
Bottom Line
This double-blind, randomized controlled trial provides compelling evidence that 40 sessions of hyperbaric oxygen therapy significantly improves physical performance in middle-aged master athletes. VO2max increased with a large effect size of 0.99, while anaerobic threshold and maximal power also improved significantly. The biological mechanism appears to be enhanced mitochondrial function: respiration capacity increased (effect size 1.09) and mitochondrial mass increased 17% versus a 9% decrease in controls (p=0.0002). This is the first blinded RCT to demonstrate HBOT enhances athletic performance through measurable cellular changes. The protocol requires substantial commitment (40 hours over 2 months) but offers a novel evidence-based approach for athletes seeking to maintain or improve performance despite age-related declines.

