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Trial registered on ANZCTR
Registration number
ACTRN12619000885190
Ethics application status
Approved
Date submitted
27/05/2019
Date registered
21/06/2019
Date last updated
13/03/2020
Date data sharing statement initially provided
21/06/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Caffeine and anaerobic exercise performance: an exploration of caffeine’s effects on performance in young men and the influence of genotype on the variation in responses
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Scientific title
The effect of CYP1A2 genotype on the ergogenic effects of caffeine during anaerobic exercise
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Secondary ID [1]
298301
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Exercise performance
312931
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Condition category
Condition code
Musculoskeletal
311422
311422
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0
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Normal musculoskeletal and cartilage development and function
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Metabolic and Endocrine
311638
311638
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0
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Normal metabolism and endocrine development and function
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Caffeine supplementation.
Dose: 3 mg per kg of body weight
The duration of administration: only on one occasion.
Mode of administration: oral tablet.
Wash out period between the caffeine and placebo conditions is from 4 to 7 days.
The CYP1A2 genotype will be assessed using a buccal swab sample collected before the caffeine and placebo conditions.
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Intervention code [1]
314536
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Other interventions
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Comparator / control treatment
Placebo,
Composition of the placebo treatment: glucose capsule,
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Primary Outcome 1: vertical jump height and power assessed using a countermovement jump on a force platform.
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Assessment method [1]
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Timepoint [1]
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One hour post caffeine and placebo ingestion.
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Primary outcome [2]
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Primary Outcome 2: barbell velocity in the bench press exercise assessed using linear position transducers.
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Assessment method [2]
320340
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Timepoint [2]
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One hour post caffeine and placebo ingestion.
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Primary outcome [3]
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Primary Outcome 3: maximal number of repetitions in an upper-body muscle endurance test.
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Assessment method [3]
320341
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Timepoint [3]
320341
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One hour post caffeine and placebo ingestion.
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Secondary outcome [1]
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Secondary Outcome 1: side-effects to caffeine ingestion such as tachycardia, self-reported by the participants.
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Assessment method [1]
370691
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Timepoint [1]
370691
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Immediately post testing and upon waking up in the morning after testing.
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Secondary outcome [2]
371274
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Primary Outcome 4: mean and peak power in the Wingate test.
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Assessment method [2]
371274
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Timepoint [2]
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One hour post caffeine and placebo ingestion.
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Eligibility
Key inclusion criteria
The sample size will consist of resistance-trained men. Resistance-trained men will be defined as having a minimum of 6 months of resistance training experience with a minimum weekly training frequency of two times on most weeks.
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Minimum age
18
Years
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Maximum age
40
Years
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Sex
Males
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
The exclusion criteria will be: (1) current smoker; (2) prior or current use of anabolic steroids; and (3) existence of health limitations.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation is not concealed.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a randomisation table created by computer software (i.e. computerised sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
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Intervention assignment
Crossover
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Other design features
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Phase
Phase 0
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
In order to calculate the sample size, we used the G*Power software, version 3.1. The expected effect size was 0.25, which is the average effect size across all meta-analyses that examined the effects of caffeine on exercise performance (Grgic et al. 2019). Here, the alpha error level was set at 0.05 and the statistical power was at 80%. The correlation between repeated measures was set at 0.75 which was determined by our previously published data (Grgic and Mikulic, 2017) and previous review papers (Polito et al., 2016). Based on this power analysis, the total required sample size for this study is 18 participants. Two-way ANOVAs (experimental treatment x genotype group) will be done for the analysis of the data. In addition, absolute and relative effect sizes (i.e. absolute differences between means and Cohen’s d values, respectively) will be calculated.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
10/07/2019
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Actual
1/08/2019
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Date of last participant enrolment
Anticipated
1/03/2020
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Actual
25/11/2019
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Date of last data collection
Anticipated
1/04/2020
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Actual
30/11/2019
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Sample size
Target
18
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Accrual to date
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Final
22
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment postcode(s) [1]
26560
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3011 - Footscray
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Recruitment postcode(s) [2]
26561
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3032 - Maribyrnong
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Victoria University
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Address [1]
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PO Box 14428, Melbourne, Vic 8001, Australia; Street address: Footscray Park Campus, Ballarat Road, Footscray 3011
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Country [1]
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Australia
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Primary sponsor type
University
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Name
Victoria University
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Address
PO Box 14428, Melbourne, Vic 8001, Australia; Street address: Footscray Park Campus, Ballarat Road, Footscray 3011
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
302791
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Address [1]
302791
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Country [1]
302791
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Victoria University Human Research Ethics Committee
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Ethics committee address [1]
303421
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PO Box 14428, Melbourne, Vic 8001, Australia; Street address: Footscray Park Campus, Ballarat Road, Footscray 3011
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Ethics committee country [1]
303421
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Australia
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Date submitted for ethics approval [1]
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27/02/2019
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Approval date [1]
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01/07/2019
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Ethics approval number [1]
303421
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Summary
Brief summary
The aim of the study will be to investigate the effects of caffeine (3 mg/kg 60 min pre-exercise) on vertical jump performance, movement velocity in resistance exercise, muscular endurance, and power output. Additionally, the aim is to explore if the inter-individual variation in responses to caffeine ingestion influenced by variations in genotype. The study hypothesis is that individuals classified as AA genotype will experience greater improvements in exercise performance following caffeine ingestion than those with AC and CC genotypes.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Prof David Bishop
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Address
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Victoria University, Melbourne
Footscray Park Campus | Ballarat Road | Footscray VIC 3001
PO Box 14428
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Country
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Australia
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Phone
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+61 0435 962 364
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Jozo Grgic
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Address
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Victoria University, Melbourne
Footscray Park Campus | Ballarat Road | Footscray VIC 3001
PO Box 14428
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Country
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Australia
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Phone
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+61 0459337908
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Jozo Grgic
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Address
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Victoria University, Melbourne
Footscray Park Campus | Ballarat Road | Footscray VIC 3001
PO Box 14428
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Country
93624
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Australia
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Phone
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+61 0459337908
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Fax
93624
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
All data.
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When will data be available (start and end dates)?
Immediately following publication, no end date.
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Available to whom?
Only researchers who provide a methodologically sound proposal.
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Available for what types of analyses?
Only to achieve the aims in the approved proposal.
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How or where can data be obtained?
Individual participant data will be available based on a request to the corresponding author.
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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