- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06363669
Effects of Caffeine-based Supplement on Physical Performance
April 8, 2024 updated by: University School of Physical Education, Krakow, Poland
Acute Effects of Multi-ingredient Pre-workout Dietary Supplement on Physical Performance in Untrained Men
The aim of the study was to determine the acute effects of multi-ingredient pre-workout supple-ment (MIPS) containing: beta-alanine, taurine, caffeine, L-tyrosine, and cayenne pepper (capsaicin) on physical performance in untrained men
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The aim of our study was to determine the acute effects of commercially available multi-ingredient pre-workout supple-ment (MIPS) containing: beta-alanine, taurine, caffeine, L-tyrosine, and cayenne pepper (capsai-cin) on physical performance in untrained men.
The aerobic and anaerobic capacity was determined after ingestion of MIPS.
A randomized, crossover, single-blind design was used to evaluate the effects of the dietary supplement on physical performance.
The participants performed the exercise test twice, in random order: as a control test and after supplement administration (MIPS).
The measurements took place over two consecutive days.
Somatic measurements were taken on the same day that the first all-out test was performed.
Twelve young healthy men, without medical contraindications to supramaximal and maximal intensity exercise, participated in the study.
The exercise tests took place under medical supervision.
Study Type
Interventional
Enrollment (Actual)
12
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Krakow, Poland, 31-571
- University School of Physical Education in Cracow
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
lack of neuromuscular and musculoskeletal disorders; no medication nor dietary supplements used within the previous month which could potentially affect the study outcomes and self-described good health status. An additional inclusion criterion was the small amount of caffeine consumed per day, i.e. only one caffeinated coffee drink per day or less.
Exclusion Criteria:
consumption of energy drinks
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: control group
Group with placebo treatment (100 ml of orange-flavored water without any additional substances (0 kcal))
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Experimental: group with MIPS supplementation
Group with supplementation.
Supplement was commercially available and dispensed without a prescription.
The dietary supplement contained in one dose (30ml): beta-alanine 3000 mg, taurine 1000 mg, caffeine 290 mg, L-tyrosine 125 mg, and cayenne pepper extract (Capsicum annuum L.) 4.2 mg (of which 8% capsaicin).
The supplement was mixed with water; in total, participants were given 100 ml of liquid to drink, 30 minutes before the warm-up for the all-out anaerobic test.
|
The participants performed the exercise twice, in random order: as a control test and after supplement administration.
The acute effects of MIPS supplementation (beta-alanine 3000 mg, taurine 1000 mg, caffeine 290 mg, L-tyrosine 125 mg, and cayenne pepper extract (Capsicum annuum L.) 4.2 mg (of which 8% capsaicin)) on aerobic and anaerobic performance were evaluated in untrained men
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
anaerobic power
Time Frame: one day every 30 minutes
|
Anaerobic power (anaerobic capacity) was determined twice (pre and post) dietary supplementation on one day.
The anaerobic test was performed before supplemenation and 30 minutes after.
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one day every 30 minutes
|
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aerobic power
Time Frame: one day every 30 minutes
|
Aerobic power (aerobic capacity) was determined twice (pre and post) dietary supplementation on one day.
The anaerobic test was performed before supplemenation and 30 minutes after.
|
one day every 30 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Marcin Maciejczyk, prof.dr, University of Physical Education, Kraków, Poland
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 15, 2018
Primary Completion (Actual)
March 30, 2024
Study Completion (Actual)
March 30, 2024
Study Registration Dates
First Submitted
April 8, 2024
First Submitted That Met QC Criteria
April 8, 2024
First Posted (Actual)
April 12, 2024
Study Record Updates
Last Update Posted (Actual)
April 12, 2024
Last Update Submitted That Met QC Criteria
April 8, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1_CAF_AWF
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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