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Hydrogenology
Source-linked study record

Drinking hydrogen water enhances endurance and relieves psychometric fatigue: a randomized, double-blind, placebo-controlled study

Mikami T, Tano K, Lee H, Lee H, Park J, Ohta F, LeBaron TW, Ohta S. · Can J Physiol Pharmacol. 2019;97(9):857-862.

HumanH₂-rich waterPublished 2019Source checked
Study record, not medical adviceThis record reports what the source states. It is not medical advice and does not establish that molecular hydrogen is effective, safe or appropriate for any person.
Quick summary

Study at a glance

This publication describes two separate exercise experiments. Among 99 untrained adults, hydrogen water favored one fatigue score but did not improve estimated aerobic capacity. Among 60 fitness-club members, estimated aerobic capacity and perceived exertion favored hydrogen. These short tests used estimated oxygen capacity and subjective scores; they do not establish a lasting health or training benefit.

Source data warningOne protocol sentence prints 1.0 mg/mL, unlike the preparation description of 1 mg/L (1 ppm). The experiments are separate parallel comparisons, not a conventional crossover, and VO₂max was estimated rather than directly measured.
Evidence type

Human

Population or model

Experiment 1: untrained adults aged 40–70. Experiment 2: fitness-club members aged 20–69, including men and women.

Intervention and dose

Experiment 1: 500 mL water containing 0.8 mg/L (0.8 ppm) H₂, 30 minutes before approximately 10 minutes of submaximal cycling; all received placebo at the initial visit, followed by hydrogen or placebo two weeks later. Experiment 2: 500 mL containing 1.0 mg/L (1.0 ppm), 10 minutes before 11 minutes of cycling; the second randomized visit was one week after an initial placebo visit. · Experiment 1: 0.8 mg/L (0.8 ppm). Experiment 2: 1.0 mg/L (1.0 ppm), supported by the preparation description. A protocol sentence prints 1.0 mg/mL instead, an unresolved source unit typo.

Duration

Acute dosing around two exercise visits: two weeks apart in Experiment 1 and one week apart in Experiment 2. Cycling tests lasted approximately 10 and 11 minutes respectively.

Reported result

Experiment 1: estimated VO₂max did not differ significantly. VAS fatigue change favored hydrogen (P = 0.046), as did heart-rate change (P = 0.015); overall Borg difference was nonsignificant. Higher-baseline-fatigue subgroup analyses were exploratory. Experiment 2: estimated VO₂max change favored hydrogen (P = 0.015; relative change P = 0.019), and Borg RPE change P = 0.00078; age-decade subgroup differences were nonsignificant. Exact between-arm mean differences were not printed in the checked narrative/captions and were not reconstructed from graphs. In the separate 4-volunteer breath substudy, 1.2 ppm water at 0.012 mg H₂/kg produced a breath peak at 10–20 minutes and above-baseline readings at 30–40 minutes; this does not establish universal whole-body retention.

Main limitation

The checked source is author revision R1, not the final typeset article. Two heterogeneous cohorts/protocols are not a pooled 159-person replication. Outcomes were estimated aerobic capacity and subjective fatigue, with exploratory subgroup/multiple comparisons. Five randomized Experiment 1 participants were not analyzed. A unit typo and paired-test wording for group comparisons remain concerns; formal statistical appraisal was not completed. Commercial support and patent interests were declared.

Evidence and classification

What kind of evidence is this?

Evidence type

Human

Reported design

Two distinct randomized, double-blind parallel comparisons of change from an initial placebo-only visit to a second randomized visit. Participants did not all receive both hydrogen and placebo in a conventional crossover.

Research topic

Exercise and recovery

Administration form

H₂-rich water

Information not yet classified

Some editorial classification fields are still pending. The source-reported outcomes and result are shown below; Hydrogenology does not infer a positive or negative signal from prose automatically.

Reported in the source

Methods

Population or model

Experiment 1: untrained adults aged 40–70. Experiment 2: fitness-club members aged 20–69, including men and women.

Sample

Experiment 1: 131 enrolled; 18 cancelled and 9 were excluded for high blood pressure; 104 randomized. Two missing-data cases and three high-blood-pressure exclusions before the second test left 99 analyzed (52 hydrogen, 47 placebo). Experiment 2: 60 selected and randomized (30 per arm), all completed; 15 men and 15 women per arm. A separate breath substudy involved 4 volunteers.

Duration

Acute dosing around two exercise visits: two weeks apart in Experiment 1 and one week apart in Experiment 2. Cycling tests lasted approximately 10 and 11 minutes respectively.

Intervention

Experiment 1: 500 mL water containing 0.8 mg/L (0.8 ppm) H₂, 30 minutes before approximately 10 minutes of submaximal cycling; all received placebo at the initial visit, followed by hydrogen or placebo two weeks later. Experiment 2: 500 mL containing 1.0 mg/L (1.0 ppm), 10 minutes before 11 minutes of cycling; the second randomized visit was one week after an initial placebo visit.

Hydrogen form

Molecular hydrogen dissolved in drinking water; two separate cohorts and protocols.

Dose or H₂ specification

Experiment 1: 0.8 mg/L (0.8 ppm). Experiment 2: 1.0 mg/L (1.0 ppm), supported by the preparation description. A protocol sentence prints 1.0 mg/mL instead, an unresolved source unit typo.

Comparator

The same water without H₂ in identical packages; each experiment used its own parallel comparison.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Estimated VO₂max from a submaximal ergometer heart-rate algorithm, not direct oxygen-consumption measurement; Borg perceived exertion and VAS psychometric fatigue.

Reported result

Experiment 1: estimated VO₂max did not differ significantly. VAS fatigue change favored hydrogen (P = 0.046), as did heart-rate change (P = 0.015); overall Borg difference was nonsignificant. Higher-baseline-fatigue subgroup analyses were exploratory. Experiment 2: estimated VO₂max change favored hydrogen (P = 0.015; relative change P = 0.019), and Borg RPE change P = 0.00078; age-decade subgroup differences were nonsignificant. Exact between-arm mean differences were not printed in the checked narrative/captions and were not reconstructed from graphs. In the separate 4-volunteer breath substudy, 1.2 ppm water at 0.012 mg H₂/kg produced a breath peak at 10–20 minutes and above-baseline readings at 30–40 minutes; this does not establish universal whole-body retention.

Extraction completeness

The available main full text was reviewed for methods, results, limitations and declarations. Uncertainties, supplementary-source limits and conflicting findings are stated in this record.

Reported adverse events

Systematic adverse-event assessment was not reported; absence of a harms statement does not establish absence of harm.

A reported association, difference or mechanism is not automatically a clinical benefit.

Interpretation limits

Limitations and applicability

Main methodological cautions

The checked source is author revision R1, not the final typeset article. Two heterogeneous cohorts/protocols are not a pooled 159-person replication. Outcomes were estimated aerobic capacity and subjective fatigue, with exploratory subgroup/multiple comparisons. Five randomized Experiment 1 participants were not analyzed. A unit typo and paired-test wording for group comparisons remain concerns; formal statistical appraisal was not completed. Commercial support and patent interests were declared.

Applies directly to

Short-term responses in the two reported adult exercise cohorts. Neither direct VO₂max, lasting training benefit nor clinical efficacy was established.

Funding and support

Experiment 1 was sponsored by a hydrogen-water consortium: ITO EN, Melodian, Kenkoukazoku, ABIST H&F and Medisol. Medisol and Blue Mercury donated water.

Conflicts of interest

K. Tano and S. Ohta were inventors on a patent application; F. Ohta was a hydrogen-related consultant. Other authors declared no conflict.

No single-study GRADE certainty rating is assigned. Read how records and evidence assessments are prepared.

Sources and status

Sources and record status

Identifiers

PMID: 31251888 · DOI: 10.1139/cjpp-2019-0059

Publisher access

Complete 28-page author manuscript, revision R1 submitted 3 May 2019, in the University of Toronto repository; marked Draft, not the final typeset article. The supplementary figure is included in this manuscript.

Editorial verification

AI-assisted editorial review of the available main full text, 29 October 2026. No independent clinical or statistical assessment has been performed.

Source sections checked

Author manuscript Methods, pages 4–8; Results 9–10; Discussion 10–13; conflicts/funding 14; Table 1, page 21; figure captions 22–23 and all figure pages.

Extraction basis

AI-assisted editorial review of the available main full text, 29 October 2026. Complete 28-page author manuscript, revision R1 submitted 3 May 2019, in the University of Toronto repository; marked Draft, not the final typeset article. The supplementary figure is included in this manuscript.

Registry / related-source limitations

UMIN000029062 is article-reported; prospective registration timing was not independently confirmed. A 2021 discussion (DOI 10.1139/cjpp-2021-0031) raises interpretation concerns; its full text was not independently reviewed.

Last reviewed

29 October 2026

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