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Study to Analyze the Aerobic Performance Efficacy of Chronic Intake With a β-alanine Supplement in Recreational Cyclists

Randomized Clinical Trial to Analyze the Efficacy of Chronic Intake of Different Doses of a β-alanine Supplement on Aerobic Performance in Recreational Long-Distance Road Cyclists

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06167395
Acronym
B-AC3
Enrollment
75
Registered
2023-12-12
Start date
2023-12-04
Completion date
2024-03-29
Last updated
2024-05-17

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

Conditions

Beta Alanine Supplementation

Keywords

Aerobic Performance, Beta Alanine, Supplementation

Brief summary

Randomized, controlled, double-blind, double-blind clinical trial, with three parallel arms depending on the product consumed (experimental product dose 1 and dose 2 and placebo product) and single-center, to measure the efficacy of a sustained release beta alanine on the aerobic performance efficacy in recreational cyclist

Detailed description

Subjects meeting the selection criteria will be randomly assigned to each of the study groups (investigational product dose 1 or dose 2, or placebo, depending on the group to which they have been assigned). The product to be consumed is beta alanine. Participants will consume the product for 30 days. They will have to take 4 intakes every three hours, being the first intake two hours after waking up. The study subjects will have to make 2 visits to the laboratory. At the first and last visit, their aerobic performance will be evaluated by an incremental test to exhaustion with gas analysis.

Interventions

DIETARY_SUPPLEMENTBeta Alanine high dose

Subjects should consume 4 intakes of 5 g of beta alanine every 3 hours each day.

DIETARY_SUPPLEMENTBeta Alanine low dose

Subjects should consume 4 intakes of 2,5 g of beta alanine every 3 hours each day.

DIETARY_SUPPLEMENTControl product

Subjects should consume 4 intakes of 2,5 g of wheat semolina every 3 hours each day.

Sponsors

Universidad Católica San Antonio de Murcia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
MALE
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Male cyclists with more than two years of cycling experience. * Perform tests without fatigue. * Road bike training at least twice a week.

Exclusion criteria

* Participants with chronic illness. * Have a long-term injury that prevents you from training in the previous month. * Inability to understand informed consent. * Have consumed beta alanine in the three years prior to the start of the study. * Consumption of other supplements that may alter performance.

Design outcomes

Primary

MeasureTime frameDescription
PowerChange in performance after 30 days of product consumptionMeasured using a cyclus 2 roller.
DistanceChange in performance after 30 days of product consumptionMeasured using a cyclus 2 roller.

Secondary

MeasureTime frameDescription
Aerobic thresholdIt will be measured twice, once at baseline or at the end of the study after 30 days.Through a stress test with gas analysis
Microcapillary bloodIt will be measured twice, once at baseline or at the end of the study after 30 days.This test provides biochemical variables (ABL90FLEX) with 70 ml of capillary blood.
Anaerobic tresholdIt will be measured twice, once at baseline or at the end of the study after 30 days.Through a stress test with gas analysis
Heart RateIt will be measured twice, once at baseline or at the end of the study after 30 days.The heart rate will be evaluated by means of a heart rate strap.
FatigueIt will be measured twice, once at baseline or at the end of the study after 30 days.Rate of perceived exertion
LactateIt will be measured twice, once at baseline or at the end of the study after 30 days.Lactate levels will be measured using the Lactate Pro 2
Maximum oxygen consumptionIt will be measured twice, once at baseline or at the end of the study after 30 days.Through a stress test with gas analysis

Countries

Spain

Outcome results

None listed

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