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Hydrogen-rich Water and Appetite in Obesity

The Effects of 8-week Hydrogen-rich Water Consumption on Body Composition, Appetite and Obesity-specific Quality of Life, and Circulating Glucagon-like Peptide-1 in Obese Men and Women (Hydrappet): a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06722326
Acronym
HYDRAPPET
Enrollment
36
Registered
2024-12-09
Start date
2024-05-15
Completion date
2024-12-30
Last updated
2025-01-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

dihydrogen, appetite, LDL cholesterol, supplementation

Brief summary

The main goal of this study is to investigate how dihydrogen supplementation impacts body composition, appetite, quality of life specific to obesity, and levels of the hormone GLP-1 in men and women with obesity. This randomized controlled trial aims to explore whether dihydrogen can improve these health indicators.

Detailed description

The primary aim of this randomized controlled trial is to evaluate the effects of dihydrogen supplementation on body composition indices, appetite, obesity-specific quality of life, and circulating GLP-1 levels in obese men and women

Interventions

DIETARY_SUPPLEMENTDietary Supplement: Hydrogen-rich water

Hydrogen-rich water with 12 mg of hydrogen per serving

DIETARY_SUPPLEMENTDietary Supplement: Control water

Control water with 0 mg of hydrogen per serving

Sponsors

University of Novi Sad, Faculty of Sport and Physical Education
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-65 years * Body fat \> 30% in women and \> 25% in men * Not physically active * Informed consent signed

Exclusion criteria

* Major chronic disease and acute injuries * History of dietary supplement use during the past 4 weeks * History of obesity pharmaceuticals use during the past 8 weeks * No consent to randomization * Participation in other studies

Design outcomes

Primary

MeasureTime frameDescription
AppetiteChange from baseline appetite at 8 weeksTotal scores for appetite as assessed by the the Food Cravings Questionnaire (FCQ)

Secondary

MeasureTime frameDescription
Body fatChange from baseline body fat at 8 weeksPercentage of body fat as assessed by a multifrequency bioelectrical impedance analyzer
Serum GLP-1Change from baseline GLP-1 at 8 weeksSerum levels of glucagon-like peptide-1 (GLP-1)
Obesity-related quality or lifeChange from baseline total scores for obesity-related quality of life at 8 weeksTotal scores for obesity-related quality of life as assessed by the The Impact of Weight on Quality of Life-Lite (IWQOL-Lite) questionnaire

Countries

Serbia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026