Caffeine Kinetics and CrossFit®-Specific Performance

NCT05516212 · Status: RECRUITING · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2024-05-16

No results posted yet for this study

Summary

The study aims at assessing the relation between caffeine (CAF) and paraxanthine (PAX) kinetics after acute ingestion of caffeine (3 mg/kg body mass) in the form or mono- or multi-ingredient preparations and CrossFit®-specific performance or selected indicators of psychophysiological state. Blood indicators of muscle damage/recovery, acid-base balance and electrolytes levels will be evaluated. The impact of genetic variations in the polymorphisms rs5751876 in ADORA2A gene and rs762551 in CYP1A2 on CAF/PAX kinetics will be considered.

Conditions

  • Supplementation
  • Sports Nutrition
  • Ergogenic Support
  • Discipline-specific Performance

Interventions

DIETARY_SUPPLEMENT

CAFMONO supplementation

CAFMONO supplementation - random blind acute intake of in individual dose providing 3mg/kg BM of CAF. CAFMONO - Caffeine (anhydrous caffeine), Ostrovit Sp. z o.o., Zambrów, POLAND

DIETARY_SUPPLEMENT

CAFMIPS_1 supplementation

CAFMIPS\_1 supplementation - random blind acute intake of in individual dose providing 3mg/kg BM of CAF. CAFMIPS\_1 - Olimp Redweiler, Olimp Laboratories Sp. z o.o., Dębica, POLAND CAFMIPS\_1 - Olimp Redweiler, Olimp Laboratories Sp. z o.o., Dębica, POLAND

DIETARY_SUPPLEMENT

CAFMIPS_2 supplementation

CAFMIPS\_2 supplementation - random blind acute intake of in individual dose providing 3mg/kg BM of CAF. CAFMIPS\_2 - Muscle Clinic Furious, Noblepharma UG, BerlinVertrieb, GERMANY.

DIETARY_SUPPLEMENT

Placebo treatment

Placebo treatment - random blind acute intake of placebo preparation. Placebo will match the remaining test preparations with taste, colour and consistency, however it will be free of caffeine and any other substances possessing ergogenic potential.

Sponsors & Collaborators

  • National Science Centre, Poland

    collaborator OTHER_GOV
  • Poznan University of Life Sciences

    collaborator OTHER
  • Poznan University of Physical Education

    lead OTHER

Principal Investigators

  • Krzysztof Durkalec-Michalski, Prof., PhD · Department of Sports Dietetics, Poznan University of Physical Education

  • Paulina M Nowaczyk, PhD · Department of Sports Dietetics, Poznan University of Physical Education

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-06-29
Primary Completion
2024-07-29
Completion
2024-07-30

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05516212 on ClinicalTrials.gov