- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06788015
Hydrogen-Infused Water for Endurance Performance, Body Hydration Biomarkers, and Health-Related Quality of Life (HYDRO2EAU)
December 15, 2025 updated by: University of Novi Sad, Faculty of Sport and Physical Education
The Effects of Hydrogen-Infused Water on Endurance Performance, Body Hydration Biomarkers, and Health-Related Quality of Life in Healthy Young Men and Women (HYDRO2EAU): A Randomized-Controlled Clinical Trial
The study investigates the impact of 4-week hydrogen-infused water consumption on various health and performance outcomes.
Conducted with healthy young adults, the trial assesses endurance performance, hydration biomarkers, and health-related quality of life.
Participants are randomized into intervention and control groups, with outcomes measured over a specified period.
The findings aim to elucidate whether hydrogen-infused water water provides significant benefits for physical performance, hydration status, and overall well-being compared to standard hydration methods.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
10
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Vojvodina
-
Novi Sad, Vojvodina, Serbia, 21000
- FSPE Applied Bioenergetics Lab
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Age 18.0 - 29.9 years
- Body mass index 18.5 - 24.9 kg/m2
- Collegiate athletes with training experience >3 years
- Weekly exercise > 5 hours
- Given written informed consent
Exclusion Criteria:
- Major chronic diseases or acute disorders
- History of dietary supplement usage in the 4 weeks preceding the study initiation
- Unwillingness to return for a follow-up
- Participation in other clinical trials
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Hydrogen-infused water
One can of hydrogen-infused water consumed before breakfast and dinner
|
Water containing molecular hydrogen
|
|
Placebo Comparator: Placebo
One can of hydrogen-free water consumed before breakfast and dinner
|
Water containing no molecular hydrogen
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time to exhaustion
Time Frame: Change from baseline time to exhaustion at 4 weeks
|
Running time to exhaustion at treadmill
|
Change from baseline time to exhaustion at 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Total body water
Time Frame: Change from baseline total body water at 4 weeks
|
Level of total body water
|
Change from baseline total body water at 4 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
36-Item Short Form Health Survey
Time Frame: Change from baseline 36-Item Short Form Health Survey total score at 4 weeks
|
Short Form Health Survey total score, minimum and maximum possible score of between 0 and 100, with higher scores mean better outcome
|
Change from baseline 36-Item Short Form Health Survey total score at 4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 15, 2024
Primary Completion (Actual)
February 28, 2025
Study Completion (Actual)
April 15, 2025
Study Registration Dates
First Submitted
January 16, 2025
First Submitted That Met QC Criteria
January 16, 2025
First Posted (Actual)
January 22, 2025
Study Record Updates
Last Update Posted (Actual)
December 22, 2025
Last Update Submitted That Met QC Criteria
December 15, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- THIC-1-24
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Data obtained through this study may be provided to qualified researchers with academic interest in hydrogen research in biomedicine.
Data will be coded, with no PHI included.
Approval of the request and execution of all applicable agreements are prerequisites to the sharing of data with the requesting party.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Exercise Overtraining
-
Indonesia UniversityCompletedSports Physical Therapy | Military Activity | Exercise OvertrainingIndonesia
-
KTO Karatay UniversityRecruiting
-
National Yang Ming UniversityRecruitingStressor, Psychological | Exercise OvertrainingTaiwan
-
Ankara UniversityCompleted
-
Charite University, Berlin, GermanyGerman Sport University, CologneEnrolling by invitationMuscle Atrophy | Myotonia | Stiffness; Spine | Exercise OvertrainingGermany
-
King Saud UniversityCompletedOsteoporosis | Exercise Overtraining | Vitamin D 25-Hydroxylase Deficiency
-
Association Tunisienne d'Etude & de Recherche sur...RecruitingObesity | Cardiometabolic Syndrome | Exercise Overtraining | EnjoymentTunisia
-
Poznan University of Physical EducationCompletedOvertraining SyndromePoland
-
University of ThessalyUnknown
Clinical Trials on Hydrogen-infused water
-
Kaohsiung Medical University Chung-Ho Memorial...Active, not recruitingQuality of Life | Pain | Head and Neck Cancer | Oral MucositisTaiwan
-
Navy General Hospital, BeijingRecruitingChronic Graft-versus-host DiseaseChina
-
University of Novi Sad, Faculty of Sport and Physical...Completed
-
Stony Brook UniversityNatural Wellness Now Health ProductsRecruitingMyalgic Encephalomyelitis/Chronic Fatigue SyndromeUnited States
-
Stony Brook UniversityCompletedChronic Fatigue SyndromeUnited States
-
Kaohsiung Medical University Chung-Ho Memorial...Not yet recruitingPostoperative Pain | Oral Cancer | Oral Squamous Cell Carcinoma (OSCC) | Free Flap Reconstruction | Postoperative Oral Mucositis
-
Qingdao UniversityQingdao Hiser Medical GroupRecruitingType 2 DiabetesChina
-
Sun JiaRecruiting
-
Center for Health Sciences, SerbiaNot yet recruiting
-
University of Novi Sad, Faculty of Sport and Physical...Completed