- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06610110
Caffeine, CYPA12 and Resistance Exercise
Influence of CYP1A2 on the Acute Effect of Caffeine Intake on Resistance Exercise
Introduction: Several studies have evaluated and confirmed the ergogenic effect of acute caffeine intake on sports performance, specifically on strength and power performance. However, it remains to be elucidated how CYP1A2 polymorphism influences the acute effects of caffeine on this type of exercise.
Objectives: The present study aims to analyze the effects of acute caffeine intake on muscular strength, power, and endurance performance according to CYP1A2 polymorphism in men and women.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Madrid
-
Alcalá de Henares, Madrid, Spain, 28805
- Facultad de Medicina y Ciencias de la Salud. Universidad de Alcalá
-
Alcalá de Henares, Madrid, Spain
- Facultad de Medicina y Ciencias de la Salud. Universidad de Alcalá
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age between ≥ 18 and ≤ 35 years.
- Body mass index (BMI) lower than 25 kg/m².
- Physically active subjects (≥150 min/week of moderate exercise).
- Healthy men and women without neurological, cardiometabolic, immunological, or physical conditions that prevent them from performing physical exercise.
- Participants capable of performing the tests.
Exclusion Criteria:
- History of neuromuscular, cardiac, or diseases that could affect liver or muscle metabolism.
- Use of drugs or other stimulants that interfere with caffeine intake and intestinal absorption during the tests and study.
- Body mass index (BMI) ≥ 25 kg/m².
- Having undergone prolonged periods of forced physical inactivity during the 6 months prior to the study.
- Performing strenuous exercise within 48 hours prior to the tests.
- Failing to replicate the same food intake on the two experimental days.
- Consuming caffeine after 6 PM on the day prior to training or testing.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Genotype AA - Male - Caffeine
|
Acute caffeine intake (3 mg/kg)
|
|
Experimental: Genotype AC or CC - Male - Caffeine
|
Acute caffeine intake (3 mg/kg)
|
|
Placebo Comparator: Genotype AA - Male - Placebo
|
Placebo (3 mg/kg maltodextrin)
|
|
Placebo Comparator: Genotype AC or CC - Male - Placebo
|
Placebo (3 mg/kg maltodextrin)
|
|
Experimental: Genotype AA - Female - Caffeine
|
Acute caffeine intake (3 mg/kg)
|
|
Experimental: Genotype AC or CC - Female - Caffeine
|
Acute caffeine intake (3 mg/kg)
|
|
Placebo Comparator: Genotype AA - Female - Placebo
|
Placebo (3 mg/kg maltodextrin)
|
|
Placebo Comparator: Genotype AC or CC - Female - Placebo
|
Placebo (3 mg/kg maltodextrin)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
cyp1a2 polymorphism
Time Frame: Before the beginning of the trial
|
Using saliva sample and PCR
|
Before the beginning of the trial
|
|
Mean velocity at different %1RM
Time Frame: Through study completion, an average of 2 weeks
|
Measuring bar mean velocity desplacement during bench press and back squat exercises.
|
Through study completion, an average of 2 weeks
|
|
Peak velocity at different %1RM
Time Frame: Through study completion, an average of 2 weeks
|
Measuring bar peak velocity and time to reach peak velocity of bar desplacement during bench press and back squat exercises.
|
Through study completion, an average of 2 weeks
|
|
Mean power output at different %1RM
Time Frame: Through study completion, an average of 2 weeks
|
Measuring during bench press and back squat exercises.
|
Through study completion, an average of 2 weeks
|
|
Peak power output and time to reach peak power output at different %1RM
Time Frame: Through study completion, an average of 2 weeks
|
Measuring during bench press and back squat exercises.
|
Through study completion, an average of 2 weeks
|
|
Number of repetitions performed in 1 set at 65%1RM until task failure
Time Frame: Through study completion, an average of 2 weeks
|
In bench press and back squat exercises
|
Through study completion, an average of 2 weeks
|
|
Bar velocity deplacement performed in 1 set at 65%1RM until task failure
Time Frame: Through study completion, an average of 2 weeks
|
In bench press and back squat exercises
|
Through study completion, an average of 2 weeks
|
|
Power output generated in 1 set at 65%1RM until task failure
Time Frame: Through study completion, an average of 2 weeks
|
In bench press and back squat exercise
|
Through study completion, an average of 2 weeks
|
|
Maximal Fat Oxidation Rate (MFO)
Time Frame: Through study completion, an average of 2 weeks
|
g/min (MFO) using a metabolic chart.
|
Through study completion, an average of 2 weeks
|
|
Resting Metabolic Rate (RMR)
Time Frame: Through study completion, an average of 2 weeks
|
Kcal at rest (RMR) using a metabolic chart.
|
Through study completion, an average of 2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mood state (tension, depression, anger, vigor, fatigue and confusion)
Time Frame: Through study completion, an average of 2 weeks
|
Participants graded a set of 29 items related to the mood on a Likert scale from 0 (not at all) to 4 (extremely) in reply to the question: How do you feel at this moment?
to assess six scales: tension, depression, anger, vigor, fatigue and confusion.
|
Through study completion, an average of 2 weeks
|
|
Adverse effects
Time Frame: Through study completion, an average of 2 weeks
|
perception of power, endurance, energy and exertion, as well as heart, muscular and gastrointestinal discomfort
|
Through study completion, an average of 2 weeks
|
|
handgrip and isometric mid-thigh pull tests
Time Frame: Through study completion, an average of 2 weeks
|
N generated
|
Through study completion, an average of 2 weeks
|
|
Vertical Jump (cm)
Time Frame: Through study completion, an average of 2 weeks
|
Through study completion, an average of 2 weeks
|
|
|
Vertical Jump (power)
Time Frame: Through study completion, an average of 2 weeks
|
Through study completion, an average of 2 weeks
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CEIP/2024/2/037
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
Clinical Trials on CYP1A2 Polymorphism
-
Poznan University of Life SciencesCompleted
-
University of AlcalaUniversity of Alcala; iSanidad+HerbalifeCompletedCYP1A2 Polymorphism | Caffeine and Resistance TrainingSpain
-
University of MonastirCompletedSchizophrenia | Clozapine | CYP1A2 Polymorphism | CYP2C19 PolymorphismTunisia
-
Affiliated Hospital of Nantong UniversityNot yet recruitingDepression | Polymerase Chain Reaction | Polymorphism, Genetic | CYP1A2 Polymorphism | Plasma Concentration | CYP2C9 Polymorphism
-
University of WashingtonNational Institute of General Medical Sciences (NIGMS)Completed
-
University of MinnesotaTerminated
-
University of WashingtonNational Institute of General Medical Sciences (NIGMS)Completed
-
Beijing Anzhen HospitalUnknownAntiplatelet Therapy | CYP2C19 PolymorphismChina
-
Infertility Treatment Center DortmundWeill Medical College of Cornell UniversityCompletedIVF | Subfertility | Estradiol Receptor Polymorphism | Progesterone Receptor PolymorphismGermany
-
Qianfoshan HospitalBeijing Micro Love Public Welfare FoundationNot yet recruitingASCVD | Gene Polymorphism
Clinical Trials on Caffeine
-
University of RochesterNot yet recruitingInfants | Neonatal Apnea
-
Indiana UniversityIndiana Clinical and Translational Sciences InstituteRecruitingPremature Birth | Respiratory Distress Syndrome | Bronchopulmonary Dysplasia | Apnea of Prematurity | Preterm Labor With Preterm DeliveryUnited States
-
Northumbria UniversityCompletedExercise | Dietary SupplementTurkey (Türkiye)
-
Istanbul University - Cerrahpasaİstanbul Yeni Yüzyıl ÜniversitesiNot yet recruitingMuscle Strength | Exercise Performance | Adaptation | Muscle HypotrophyTurkey (Türkiye)
-
Sinop UniversityCompletedAthletic Performance | Cognitive Performance | Healthy Adult FemalesTurkey (Türkiye)
-
Universidad Rey Juan CarlosEnrolling by invitationExercise | Caffeine | Ergogenics | Cycling | Fat MetabolismSpain
-
KTO Karatay UniversityRecruitingPostoperative Pain | Gastrointestinal Motility | Psychological Well-BeingTurkey (Türkiye)
-
University of Wisconsin, MadisonEunice Kennedy Shriver National Institute of Child Health and Human Development...Recruiting
-
Southern Illinois University CarbondaleCompleted
-
National Taiwan Sport UniversityCompleted