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Acute effect of pre-workout supplements on the performance of amateur athletes

Changes in performance, body composition and biochemical parameters of young adults after acute and chronic supplementation with pre-training

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2qfvyfv
Enrollment
Unknown
Registered
2020-12-07
Start date
2019-03-18
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Human Activities, Endurance Training, sports, running, Athletic Performance, Performance-Enhancing Substances

Interventions

two tests of 10 km of running, separated by at least 72 hours, on an official athletics track. First, participants ingest the Capsaicin 12 mg capsule or placebo, 45 minutes, ingest another Capsaicin 1
I03.450.642.845
I03.450.642.845.610
I03.350.311.188

Sponsors

Fundação Universidade Estadual do Piauí
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Healthy young adult man; age between 18 and 35 years old; able to run 10 km in less than 60 minutes.

Exclusion criteria

Exclusion criteria: Presence of cardiovascular or joint diseases; use of medication for continuous use; regular consumption of food supplement or stimulants.

Design outcomes

Primary

MeasureTime frame
Check if capsaicin supplementation is efficient to improve the running time in the distance of 10km for amateur athletes; a comparison will be made between the averages of the final time between the race that the participants ingested capsaicin and the race in which they took a placebo; difference between the final run time with capsaicin and placebo (negative delta value) is greater than or equal to 79.17 seconds. Statistical significance set at 0.05%.

Secondary

MeasureTime frame
Secondary outcomes are not expected.

Countries

Brazil

Contacts

Public ContactFábio Lira
fabio.lira@unesp.br+ 55-18-3229-5826

Outcome results

None listed

Source: REBEC (via WHO ICTRP)