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Trial registered on ANZCTR
Registration number
ACTRN12614000629639
Ethics application status
Approved
Date submitted
5/06/2014
Date registered
13/06/2014
Date last updated
4/05/2016
Type of registration
Retrospectively registered
Titles & IDs
Public title
Carbohydrate dependence during endurance exercise (The effect of Nicotinic acid on endurance performance in trained cyclists)
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Scientific title
The effect of Nicotinic acid on endurance performance in trained cyclists
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Secondary ID [1]
284746
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None
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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:
endurance exercise performance in healthy trained athletes
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Condition category
Condition code
Metabolic and Endocrine
292445
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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
Using a repeated measures design, we will test our hypothesis in 10 well-trained cyclists who will each perform six maximal, all-out cycling time-trials (over 60, 90 and 120 min duration), three under conditions where lipolysis and fat oxidation are ‘blocked’ and three under normal conditions (control). Lipolysis will be blocked via orally administered nicotinic acid.
1a) The dose administered for the the 60 min trial will be 20 mg/kg BM
The dose administered for the 90 min trial will be 25 mg/kg BM
The dose for the 120 min trial will be 30 mg/kg BM
b)Doses 1x10 mg/kg BM dose 30 mins before trial, 1x5 mg/kg dose 15 min before trial, and 5 mg/kg BM after completion of every 30 min of trial.
2)TT's will be conducted on a stationary bike.
3) wash out period will be at least 72 hr between trials
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Intervention code [1]
289531
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Other interventions
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Comparator / control treatment
Control conditions will be the same conditions as the experimental group but instead of taking the nicotinic acid participants will be orally administered small doses of glucose powder (placebo)
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Time to complete time trial
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Assessment method [1]
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Timepoint [1]
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compare time trial times under nicotinic acid conditions to control/placebo conditions
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Secondary outcome [1]
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Respiratory Exchange Ratio values. assessed using a Parvomedics metabolic cart.
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Assessment method [1]
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Timepoint [1]
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compare values attained during nicotinic acid conditions with values attained during control/placebo conditions. These outcome will be assessed at the completion of all trials from all subjects
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Eligibility
Key inclusion criteria
Inclusion criteria:
Aged 18-35 years
Participants must be engaged in cycling training > 200km/week.
Participants must have at least 2 years of competitive cycling experience.
VO2max of greater than 60 mL/ (kg BM/min).
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Minimum age
18
Years
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Maximum age
35
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Exclusion criteria:
Current or prior use of anabolic steroids or other prohibited substances.
Contraindications to strenuous physical activity as indicated by cardiovascular risk factor questionnaire.
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Study design
Purpose of the study
Educational / counselling / training
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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)
Initially telephone interviews, e-mail or a face to face meeting will assess suitability and if subjects comply with inclusion/exclusion criteria. Subsequently, participants will attend a physiological testing session to assess suitability for the study. The selected participants will then be informed about all the details of the study and the risks and benefits involved. A signed Informed consent document approved by the Human Ethics Committee at the Australian Catholic University will be obtained prior to any experimental trials.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
trial conditions will assigned a number (1, 2, 3, 4, 5 or 6) with each number only being used once. These 6 numbers will then be entered into a random code generator of which 10 combinations will be selected for the 10 participants. each participant will then be allocated a code and that is the order that they will complete the trials.
the method of allocation concealment we will use is numbered containers
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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 analysing the results/data
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Intervention assignment
Crossover
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
30/06/2014
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Actual
2/06/2014
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Date of last participant enrolment
Anticipated
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Actual
4/08/2014
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
10
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Accrual to date
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Final
9
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Recruitment in Australia
Recruitment state(s)
VIC
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Funding & Sponsors
Funding source category [1]
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Government body
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Name [1]
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Australian Institute of Sport
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Address [1]
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Leverrier Crescent, Bruce ACT 2617
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Country [1]
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Australia
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Primary sponsor type
University
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Name
Australian Catholic University
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Address
115 Victoria Parade Fitzroy Victoria 3065
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Country
Australia
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Secondary sponsor category [1]
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Government body
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Name [1]
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Australian Institute of Sport
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Address [1]
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Leverrier Crescent, Bruce ACT 2617
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Country [1]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Australian Catholic University Human Ethics Committee
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Ethics committee address [1]
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Manager, Ethics c/o Office of the Deputy Vice Chancellor (Research) Australian Catholic University North Sydney Campus PO Box 968 NORTH SYDNEY, NSW 2059
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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20/02/2014
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Approval date [1]
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01/04/2014
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Ethics approval number [1]
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2014 51V
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Summary
Brief summary
One of the major adaptations of muscle to endurance training is a slower utilization of carbohydrate stored in the muscle (muscle glycogen) and blood glucose and greater reliance on fat oxidation during low intensity exercise. . These adaptations are thought to play an important role in the large increase in the ability to perform prolonged strenuous exercise that occurs in response to endurance exercise training. However, the results of early studies demonstrate ‘carbohydrate dependence’ during prolonged endurance events (i.e. marathon running) lasting up to 3 hours, with little (<10%) contribution from fat to the total fuel requirements of exercise. Using a pharmacological agent Nicotinic acid(also known as Niacin or Vitamin B3) to block the breakdown and liberation of free fatty acids into the bloodstream(lipolysis) and impair rates of fat oxidation during exercise, we will test the hypothesis that carbohydrate is the predominant (>90% of total energy requirements) fuel for muscle oxidation during cycling time trials lasting from 60-120 min. Using a repeated measures design, we will test our hypothesis in 10 well-trained cyclists who, after a standardised diet/exercise control, will each perform six maximal, all-out cycling time-trials (over 60, 90 and 120 min duration), three under conditions where lipolysis and fat oxidation are ‘blocked’ and three under normal conditions (control). We hypothesise that there will be no differences in the time-trial performance for any duration, and that carbohydrate oxidation will be the major fuel for oxidative energy production.
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Trial website
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Trial related presentations / publications
Torrens, S.L., Areta, J.L., Parr, E.B., Hawley, J.A. Carbohydrate dependence during prolonged simulated cycling time trials. 2016, 116(4): 781-90.
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Public notes
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Contacts
Principal investigator
Name
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Prof John Hawley
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Address
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Australian Catholic University
Daniel Mannix Building
Level One
office 1.32
115 Victoria Parade Fitzroy Victoria 3065
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Country
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Australia
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Phone
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+61 2 9953 5552
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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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John Hawley
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Address
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Australian Catholic University
Daniel Mannix Building
Level One
office 1.32
115 Victoria Parade Fitzroy Victoria 3065
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Country
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Australia
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Phone
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+61 2 9953 5552
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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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John Hawley
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Address
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Australian Catholic University
Daniel Mannix Building
Level One
office 1.32
115 Victoria Parade Fitzroy Victoria 3065
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Country
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Australia
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Phone
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+61 2 9953 5552
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
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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