CClinicalTrials.gg
Not yet recruitingNCT07855120HRW-FOOTBALLUpdated Oct 2, 2026

Effects of Hydrogen-rich Water Consumption on Transient Fatigue During an Official Football Match: Protocol for a Randomised, Double-blind, Placebo-controlled, Parallel-group Trial

An interventional study of Hydrogen-Rich Water (HRW) and Placebo Water in Exercise-Induced Fatigue and Football Performance, sponsored by Palacky University. Not yet recruiting. Open to male participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-02.

Sponsored by Palacky University · Not applicable, Interventional, and Other

Updated Oct 2, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years and older
Sex
Male
01

Study summary

The purpose of this study is to determine whether drinking hydrogen-rich water can reduce fatigue and help football players maintain high-intensity physical activity during an official football match.

The study will include 30 male football players competing in the second and third tiers of the Czech national football league system. Participants will be randomly assigned to drink either hydrogen-rich water or placebo water. Neither the players nor the researchers conducting the assessments will know which type of water each participant receives until the study has been completed.

Participants will begin drinking the assigned water 72 hours before the match and will continue drinking it on match day. Players' physical activity and heart rate will be monitored throughout the match. The main outcome will be the distance covered at high intensity during consecutive 5-minute periods of the match. Repeated-sprint ability, jumping performance, and perceived muscle soreness will also be assessed before and after the match.

The study will compare the hydrogen-rich water and placebo groups to determine whether hydrogen-rich water helps players maintain high-intensity activity during the match and reduces short-term fatigue after the match.

Read the detailed description

Fatigue during football match play may reduce players' ability to maintain high-intensity activity, particularly following demanding periods of play and during the later stages of a match. The mechanisms contributing to fatigue are multifactorial and include metabolic, neuromuscular, and perceptual factors. Exercise-induced changes in redox homeostasis may also contribute to impaired skeletal muscle function during strenuous exercise.

Molecular hydrogen has been investigated as a potential strategy for supporting exercise performance and recovery because of its proposed effects on redox homeostasis, inflammatory pathways, and mitochondrial function. Hydrogen-rich water (HRW) provides a practical method of molecular hydrogen administration. Previous studies have reported potential effects of HRW on exercise-related outcomes, including blood lactate responses, perceived exertion, muscle soreness, and the maintenance of performance during repeated high-intensity exercise. However, evidence remains inconsistent, and it is currently unclear whether these effects translate to competitive football match play.

This study will therefore investigate whether HRW consumption influences the development of transient fatigue during an official football match. Particular attention will be given to changes in high-intensity running activity throughout the match. Continuous monitoring will allow match activity to be examined in consecutive 5-minute periods and between the first and second halves. This approach is intended to determine whether the temporal pattern of high-intensity activity differs between players receiving HRW and those receiving placebo.

In addition to match running performance, internal load and acute post-match fatigue will be evaluated. Heart rate responses will be monitored throughout the match, while repeated-sprint ability, countermovement jump performance, and perceived lower-limb muscle soreness will be assessed before and immediately after match play. Together, these measures will provide complementary information about external load, internal load, and acute neuromuscular and perceptual responses to competitive match play.

The study is intended to determine whether the effects of molecular hydrogen previously observed under controlled exercise conditions are also evident under the complex physiological and contextual demands of an official football match.

02

Conditions studied

  • Exercise-Induced Fatigue
  • Football Performance

Browse trials for

Keywords

  • molecular hydrogen
  • external load
  • recovery
  • antifatigue
  • muscle pain
03

In context

Myalgia

282 studies on the registry are indexed under Myalgia; 43 are open to participants now.

This study's planned enrollment of 30 is below the median of 44 across 241 interventional studies indexed under Myalgia.

Browse Myalgia studies →

Lead sponsor

Palacky University is the lead sponsor of 28 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Male football players aged 18 years or older.
  • Currently competing in the second or third tier of the Czech national football league system.
  • At least 15 years of football experience.
  • Participation in at least four team training sessions per week in addition to regular competitive matches.
  • Free from injury or other medical conditions that could limit participation in training, testing, or match play.
  • Willing and able to provide written informed consent.

Exclusion criteria

Exclusion Criteria:

  • Illness during the three weeks preceding the baseline assessment.
  • Injury during the three weeks preceding the baseline assessment.
  • Any injury or medical condition that could limit participation in training, testing, or match play.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Hydrogen-Rich Water (HRW)

    Participants assigned to this arm will consume hydrogen-rich water (HRW) containing 1.2-1.4 ppm dissolved molecular hydrogen. Participants will consume 1,260 mL (three 420-mL packs) at 72, 48, and 24 hours before the official football match, 840 mL (two 420-mL packs) after the pre-match warm-up, and 420 mL (one 420-mL pack) during the first half of the match.

    Dietary Supplement: Hydrogen-Rich Water (HRW)

  • Placebo comparator
    Placebo water

    Participants assigned to this arm will consume placebo water containing no dissolved molecular hydrogen (0.0 ppm). The placebo will be provided in visually identical 420-mL packs and administered according to the same supplementation schedule as the HRW intervention: 1,260 mL at 72, 48, and 24 hours before the official football match, 840 mL after the pre-match warm-up, and 420 mL during the first half of the match.

    Dietary Supplement: Placebo Water

Interventions

  • Dietary supplementHydrogen-Rich Water (HRW)

    Hydrogen-rich water containing 1.2-1.4 ppm dissolved molecular hydrogen (H₂), supplied in gas-tight 420-mL plastic-aluminium packs. Participants will consume 1,260 mL at 72, 48, and 24 hours before the official football match, 840 mL after the pre-match warm-up, and 420 mL during the first half of the match, corresponding to a total intervention volume of 5,040 mL per participant.

  • Dietary supplementPlacebo Water

    Placebo water containing no dissolved molecular hydrogen (0.0 ppm), supplied in visually identical 420-mL plastic-aluminium packs. The placebo will be administered according to the same volume and timing schedule as the hydrogen-rich water intervention, corresponding to a total intervention volume of 5,040 mL per participant.

06

What researchers measure

Primary outcomes

  1. High-Intensity Distance During Match Play

    High-intensity distance (HID), defined as the distance covered at running speeds \>14.4 km·h-¹, will be measured continuously during an official football match using a 10-Hz global positioning system (GPS; Vector S7, Catapult Sports, Melbourne, Australia). HID will be quantified in metres for consecutive 5-minute intervals throughout match play. The temporal pattern of HID will be compared between the hydrogen-rich water and placebo groups.

    Time frame: During the official football match (consecutive 5-minute intervals, up to 90 minutes)

Secondary outcomes

  1. Total Distance During Match Play

    Total distance (TD), expressed in metres, will be measured continuously using a 10-Hz GPS system and quantified in consecutive 5-minute intervals throughout the official football match.

    Time frame: During the official football match (consecutive 5-minute intervals, up to 90 minutes)

  2. PlayerLoad During Match Play

    PlayerLoad will be measured continuously using the triaxial accelerometer integrated within the Catapult Vector S7 system and quantified in consecutive 5-minute intervals throughout match play.

    Time frame: During the official football match (consecutive 5-minute intervals, up to 90 minutes)

  3. Top Speed During Match Play

    Top speed, expressed in km·h-¹, will be determined using the 10-Hz GPS system during the official football match.

    Time frame: During the official football match (up to 90 minutes)

  4. Heart Rate During Match Play

    Heart rate will be recorded continuously and expressed relative to each participant's individual peak heart rate (HRpeak). Heart rate responses will be evaluated in consecutive 5-minute intervals.

    Time frame: During the official football match (consecutive 5-minute intervals, up to 90 minutes)

  5. Repeated-Sprint Ability

    Repeated-sprint ability will be assessed using five 20-m sprints starting every 20 seconds. Performance will be expressed as total sprint time (sum of the five sprints). Acute match-induced fatigue will be evaluated as the pre- to post-match change in total sprint time.

    Time frame: Pre-match and immediately post-match

  6. Countermovement Jump Performance

    Countermovement jump performance will be assessed using an OptoJump system. Acute match-induced neuromuscular fatigue will be evaluated as the pre- to post-match change in jump performance.

    Time frame: Pre-match and immediately post-match

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Aoki, K., Nakao, A., Adachi, T., Matsui, Y., & Miyakawa, S. (2012). Pilot study: Effects of drinking hydrogen-rich water on muscle fatigue caused by acute exercise in elite athletes. Medical Gas Research, 2, 12. https://doi.org/10.1186/2045-9912-2-12 Bangsbo, J., Mohr, M., & Krustrup, P. (2006). Physical and metabolic demands of training and match-play in the elite football player. J. Sports Sci., 24(7), 665-674. https://doi.org/10.1080/02640410500482529 Beato, M., Coratella, G., Schena, F., & Hulton, A. T. (2017). Evaluation of the external and internal workload in female futsal players. Biology of Sport, 3, 227-231. https://doi.org/10.5114/biolsport.2017.65998 Botek, M., Krejci, J., McKune, A. J., Sladeckova, B., & Naumovski, N. (2019). Hydrogen Rich Water Improved Ventilatory, Perceptual and Lactate Responses to Exercise. INTERNATIONAL JOURNAL OF SPORTS MEDICINE, 40(14), 879-885. https://doi.org/10.1055/a-0991-0268 Botek, M., Krejčí, J., McKune, A., Valenta, M., & Sládečková, B. (2022). Hydrogen Rich Water Consumption Positively Affects Muscle Performance, Lactate Response, and Alleviates Delayed Onset of Muscle Soreness After Resistance Training. The Journal of Strength & Conditioning Research, 36(10). https://journals.lww.com/nsca-jscr/Fulltext/2022/10000/Hydrogen_Rich_Water_Consumption_Positively_Affects.15.aspx Bradley, P. S., & Noakes, T. D. (2013). Match running performance fluctuations in elite soccer: Indicative of fatigue, pacing or situational influences? Journal of Sports Sciences, 31(15), 1627-1638. https://doi.org/10.1080/02640414.2013.796062 Brownstein, C. G., Dent, J. P., Parker, P., Hicks, K. M., Howatson, G., Goodall, S., & Thomas, K. (2017). Etiology and Recovery of Neuromuscular Fatigue following Competitive Soccer Match-Play. Frontiers in Physiology, 8. https://doi.org/10.3389/fphys.2017.00831 Chan, A.-W., Boutron, I., Hopewell, S., Moher, D., Schulz, K. F., Collins, G. S., Tunn, R., Aggarwal, R., Berkwits, M., Berlin, J. A., Bhandari, N., But

Individual participant data

Plan to share: Yes — De-identified individual participant data underlying the results reported in the primary publication will be shared. The shared dataset will include participant characteristics, treatment allocation, match external- and internal-load variables, repeated-sprint ability, countermovement jump performance, and perceived lower-limb muscle soreness. Data will be de-identified to protect participant confidentiality.

Supporting information: Study protocol, Icf

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 2, 2026
Show all 1 update
  1. Oct 2, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07855120
Lead sponsor
Palacky University
Collaborators
University of Split
Responsible party
Karel Hulka (Palacký University Olomouc, Palacky University) — Principal investigator
First posted
Oct 2, 2026
Start date
Jan 20, 2027 (estimated)
Primary completion
Mar 15, 2027 (estimated)
Completion
Jun 10, 2027 (estimated)
Last update
Oct 2, 2026

Study contacts

Karel Hulka, PhD
Contact
karel.hulka@upol.cz
+420585636506

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion