Hydrogen-Rich Water and Resting Metabolism in Young Adults
- Conditions
- Healthy Subjects or Volunteers
- Registration Number
- NCT07098221
- Lead Sponsor
- University of Novi Sad
- Brief Summary
The H2REST trial is a randomized, double-blind, placebo-controlled crossover study investigating the acute effects of a single dose of hydrogen-rich water (HRW) on resting metabolism in healthy young adults. Participants complete two testing sessions-receiving either HRW or placebo in a randomized order-followed by standardized metabolic testing. Primary outcomes include resting energy expenditure, respiratory exchange ratio, and substrate utilization measured via indirect calorimetry. The study aims to assess whether acute HRW intake can modulate metabolic rate and fuel preference at rest, and to explore inter-individual variability in response.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 24
- Aged 18-35 years
- BMI between 18.5 and 25.0 kg/m²
- Apparently healthy, with no history of chronic disease
- Non-smoker, not currently using nicotine-containing products
- Able to provide informed consent
- Willing to refrain from alcohol, caffeine, and strenuous exercise for 24 hours before each study visit
- Able to comply with study procedures, including fasting and attending all study visits
- Diagnosed metabolic, cardiovascular, respiratory, gastrointestinal, or endocrine disorders
- Use of dietary supplements or medications affecting metabolism (within the past 2 weeks)
- Allergy or intolerance to components of the hydrogen or placebo beverages
- Pregnant or lactating
- Shift work or irregular sleep schedule
- Participation in another clinical study within the past 30 days
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Resting Energy Expenditure (REE) Participants will attend three study visits, with each intervention separated by a 7-day washout period to minimize carry-over effects. During each visit, measurements will be conducted approximately 30-60 minutes post-intervention. The measurements will be obtained during each study visit. Since this is an interventional study assessing the acute effects of molecular hydrogen, measurements will be collected three times:
At baseline, without any intervention (pre-familiarization),
After a single dose of molecular hydrogen, and
After placebo administration.
The period between each intervention will be seven days, serving as a washout period to prevent carry-over effects. All participants will be instructed to maintain their regular diet and to avoid alcohol, caffeine-containing beverages, and strenuous physical activity for at least 24 hours prior to each visit.
Measure Type: Continuous (kcal/day)
Method: Indirect calorimetry
Description: To assess the effect of acute ingestion of hydrogen-rich water versus placebo on resting energy expenditure in healthy young adults.
- Secondary Outcome Measures
Name Time Method