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Effects of Sustamine(TM) on Cycling Time Trial Performance

Effects of Sustamine(TM) on Cycling Time Trial Performance Following Prolonged Cycling

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01623947
Enrollment
14
Registered
2012-06-20
Start date
2012-06-30
Completion date
2013-05-31
Last updated
2013-04-19

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

Conditions

Healthy

Keywords

glutamine, cycling performance, mental function

Brief summary

Acute supplementation of Sustamine(TM), a combination of two amino acids, will improve cycling performance and mental acuity in a dose-dependent response.

Interventions

DIETARY_SUPPLEMENTPlacebo Beverage

1400 ml flavored, colored, artificially sweetened, non-caloric beverage divided into 6 servings provided prior to and during the 2.5 hr interval ride.

DIETARY_SUPPLEMENT2.8 g Sustamine Beverage

1400 ml flavored, colored, artificially sweetened, beverage containing 2.8 g Sustamine divided into 6 servings provided prior to and during the 2.5 hr interval ride.

DIETARY_SUPPLEMENT19.6 g Sustamine Beverage

1400 ml flavored, colored, artificially sweetened, beverage containing 19.6 g Sustamine divided into 6 servings provided prior to and during the 2.5 hr interval ride.

Sponsors

Kyowa Hakko Bio Co., Ltd.
CollaboratorINDUSTRY
University of Texas at Austin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Competitive cyclist or triathlete * Male (VO2max \>= 55 ml/kg/min) or Female (VO2max \>= 45 ml/kg/min) * Healthy * Blood pressure below 140/90 * Non-smoker

Exclusion criteria

* Anti-depressant medications * Inconsistent regular medications * Consumption performance-enhancing substances * Type I or Type II diabetes * Renal, hepatic or cardiac disease Current infectious disease

Design outcomes

Primary

MeasureTime frameDescription
Improved Time Trial PerformanceAfter 2.5 hr interval cyclingParticipants will perform an interval ride on a cycling ergometer for 2.5 hr. Intervals will be at 50% or 75% of the participant's VO2max. The time trial will consist of 4 km up a constant grade.

Secondary

MeasureTime frameDescription
Improved Mental FunctionAfter time trialMental function will be assessed using a computer-based Stroop Test. Measurements will be collected before treatment, before exercise and after exercise.

Countries

United States

Outcome results

None listed

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