Effect of β-alanine Supplementation and Training on Ergogenic Measures and Plasma Metabolites in Untrained Young Adults
1 other identifier
interventional
43
1 country
1
Brief Summary
This study enrolled untrained young adults to evaluate the effects of β-alanine supplementation combined with a structured exercise training program. Participants were randomly assigned to receive either β-alanine or a placebo while completing a six-week training regimen. Before and after the intervention, physical performance tests and blood samples were collected to assess changes in performance measures and biochemical markers in the blood. The purpose of the study was to determine how β-alanine supplementation influences exercise performance and related physiological outcomes in individuals who had not previously engaged in regular training.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2012
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2012
CompletedFirst Submitted
Initial submission to the registry
January 29, 2026
CompletedFirst Posted
Study publicly available on registry
February 11, 2026
CompletedFebruary 11, 2026
February 1, 2026
2 months
January 29, 2026
February 4, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change in maximal muscle strength
Maximal muscle strength was assessed by dynamometric measurements of maximal voluntary isometric contraction.
Baseline and 6 weeks
Change in aerobic capacity
Aerobic capacity was estimated by VO₂max derived from the 20-m multistage fitness test (shuttle run).
Baseline and 6 weeks
Secondary Outcomes (7)
Body mass index (BMI)
Baseline and 6 weeks
Body fat percentage
Baseline and 6 weeks
Forced vital capacity (FVC)
Baseline and 6 weeks
Acute blood lactate response to dynamometric exercise
Baseline and 6 weeks
Plasma β-alanine concentration
Baseline and 6 weeks
- +2 more secondary outcomes
Other Outcomes (1)
Adverse events
Up to 6 weeks
Study Arms (2)
β-Alanine Supplementation
EXPERIMENTALParticipants received β-alanine supplementation at a dose of 50 mg/kg/day, divided into multiple daily doses, in combination with a supervised six-week exercise training program.
Placebo
PLACEBO COMPARATORParticipants received a visually identical placebo following the same dosing schedule as the supplementation group, in combination with a supervised six-week exercise training program.
Interventions
β-alanine was administered orally at a dose of 50 mg/kg/day, divided into multiple daily doses and consumed with meals, throughout the six-week training intervention.
Participants received visually identical placebo capsules following the same dosing schedule as the β-alanine group during the six-week training intervention.
Eligibility Criteria
You may qualify if:
- Healthy young adults aged 18-30 years.
- Untrained individuals without participation in structured resistance or endurance training during the previous 6 months.
- Not physically inactive, but not engaged in regular structured exercise training.
- Ability to participate in a six-week supervised multicomponent exercise training program.
- Willingness to comply with study procedures, training sessions, and supplementation protocol.
- Provision of written informed consent.
You may not qualify if:
- Known cardiovascular, metabolic, neuromuscular, or musculoskeletal disease.
- Acute injury at the time of enrollment.
- Regular use of medications or dietary supplements affecting muscle metabolism or exercise performance.
- Participation in structured resistance or endurance training during the previous 6 months.
- Failure to comply with the study protocol or training requirements.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Pécs
Pécs, Hungary
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 29, 2026
First Posted
February 11, 2026
Study Start
January 1, 2012
Primary Completion
March 1, 2012
Study Completion
March 1, 2012
Last Updated
February 11, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared publicly due to data protection and privacy considerations. De-identified data may be made available upon reasonable request to the corresponding author, subject to institutional approval.