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Study Protocol on the Effects of Solid Beverage Supplementation on Body Hydration Status and Exercise Performance in Sports Scenarios

Study Protocol on the Effects of Solid Beverage Supplementation on Body Hydration Status and Exercise Performance in Sports Scenarios

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111258
Enrollment
Unknown
Registered
2025-10-28
Start date
2025-10-31
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

None listed

Interventions

water Group:Hydration During Exercise
Stachyose Group:Consumption of Stachyose-Containing Solid Beverage During Exercise
Isomaltulose Group:Consumption of Isomaltulose-Containing Solid Beverage During Exercise
Isomaltulose + CAF Group:Consumption of Isomaltulose + Caffeine-Containing Solid Beverage During Exercise

Sponsors

Beijing Sport University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 26 Years

Inclusion criteria

Inclusion criteria: In good general health. Has a stable lifestyle, characterized by a regular diet, sleep/wake cycle, and a consistent exercise routine (2-8 hours/week or >= 1 hour/day, maintained for >6 months, beyond activities of daily living), which they can commit to throughout the trial. No personal history of diabetes, impaired glucose tolerance, or other significant metabolic, digestive, endocrine, or psychiatric diseases. Has not used any nutritional supplements known to affect glucose tolerance, oral contraceptives, acetylsalicylic acid, steroids, protease inhibitors, antipsychotics, or other medications interfering with the study objectives within the past 3 months.

Exclusion criteria

Exclusion criteria: Pregnancy or lactation. Severe comorbidities involving the heart, liver, kidneys, or hematopoietic system. Presence of acute or chronic wasting diseases that may confound study outcomes. Diagnosis of a severe metabolic disorder (e.g., diabetes) or a known family history of diabetes. A history of allergic predisposition or known allergy to any component of the investigational product. Use of any substances (e.g., caffeine, nutritional supplements, or medications) that may interfere with the study's primary endpoints within one month prior to the study. Chronic medication use, heavy alcohol consumption, current smoking, or smoking cessation within the past 6 months.

Design outcomes

Primary

MeasureTime frame
Body weight;vertical jump;5km timed run;blood glucose;temperature and humidity;

Secondary

MeasureTime frame
RPE;Gastrointestinal Scale;Thirst Level Scale;body fat;

Countries

China

Contacts

Public ContactSun Ye

Beijing Sport University

sunye@bsu.edu.cn+86 132 7620 7505

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026