- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03749785
Carbohydrate Feeding Frequency, Muscle Glycogen and Exercise Capacity in Runners
October 31, 2019 updated by: James Betts, University of Bath
The Effect of Carbohydrate Feeding Frequency on Muscle Glycogen and Exercise Capacity in Runners
The aim of this study is to investigate the effects of regular sucrose feeds compared to a single large bolus given late in exercise, on muscle glycogen utilisation, exercise capacity and other markers of metabolism during running
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
7
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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-
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Bath, United Kingdom, BA2 7AY
- Department for Health, University of Bath
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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
18 years to 50 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Self-identify as a trained runner
- Regularly participate in running activity (>2 times a week)
- Participated in running based training for a minimum of 2 years
- Be willing to undertake exercise sessions until volitional exhaustion
- Be willing to have the necessary samples taken during the testing protocols
- Not a habitual smoker
- Have the capacity and willingness to provide informed consent (oral and written)
- Successful completion of the physical activity readiness questionnaire (PAR-Q)
Exclusion Criteria:
- Female
- <18 or >50 years old
- Not regularly participating in running activity (<3 times a week)
- Experience contraindications to the administration of the proposed anaesthetic (Lidocaine Hydrochloride)
- Habitual/previously habitual smoker
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: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Regular carbohydrate feeding
Ingestion of 75 g sucrose, given in regular doses for the first 75 minutes of exercise during a time to exhaustion run
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60 ml of water with 5 g sucrose given every 5 minutes 14 times up until 70 minutes followed by 5 g sucrose after 75 minutes in a 250 ml solution
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Active Comparator: Single carbohydrate bolus
Ingestion of 75 g sucrose, given in a single bolus after 75 minutes of exercise, during a time to exhaustion run
|
60 ml of water given every 5 minutes 14 times up until 70 minutes followed by 75 g sucrose after 75 minutes in a 250 ml solution
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle glycogen concentrations
Time Frame: Estimated to be between 90 and 145 minutes
|
Muscle glycogen concentration at rest, after 75 minutes of treadmill running and at volitional exhaustion.
Measured using the bergstrom needle technique for obtaining muscle biopsy samples
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Estimated to be between 90 and 145 minutes
|
Exercise capacity
Time Frame: Estimated to be between 90 and 145 minutes
|
Time to exhaustion at the pre-determined speed to elicit exhaustion after ~90 minutes when ingesting water only
|
Estimated to be between 90 and 145 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Ratings of perceived exertion
Time Frame: Estimated to be between 90 and 145 minutes
|
Subjective ratings of perceived exertion, during treadmill running.
Measured using a borg scale of 6 to 20, where 6 = no exertion at all, and 20 = maximal exertion.
|
Estimated to be between 90 and 145 minutes
|
Ratings of stomach discomfort
Time Frame: Estimated to be between 90 and 145 minutes
|
Subjective ratings of stomach discomfort during treadmill running.
Measured using a modified borg scale of 6 to 20, where 6 = no discomfort and 20 = maximal discomfort
|
Estimated to be between 90 and 145 minutes
|
Carbohydrate oxidation
Time Frame: Estimated to be between 90 and 145 minutes
|
Total carbohydrate oxidation during treadmill running.
Measured using indirect calorimetry and reported in grams.
|
Estimated to be between 90 and 145 minutes
|
Fat oxidation
Time Frame: Estimated to be between 90 and 145 minutes
|
Total fat oxidation during treadmill running.
Measured using indirect calorimetry and reported in grams.
|
Estimated to be between 90 and 145 minutes
|
Plasma glucose concentrations
Time Frame: Estimated to be between 90 and 145 minutes
|
Plasma lactate concentrations during of treadmill running.
Measured using colourimetric assay and reported in mmol/L
|
Estimated to be between 90 and 145 minutes
|
Plasma lactate concentrations
Time Frame: Estimated to be between 90 and 145 minutes
|
Plasma lactate concentrations during treadmill running.
Measured using colourimetric assay and reported in mmol/L.
|
Estimated to be between 90 and 145 minutes
|
Heart rate
Time Frame: Estimated to be between 90 and 145 minutes
|
Heart rate during treadmill running measured by telemetry and reported in beats per minute
|
Estimated to be between 90 and 145 minutes
|
Rate of oxygen consumption
Time Frame: Estimated to be between 90 and 145 minutes
|
Rate of oxygen consumption during treadmill running.
Measured using indirect calorimetry and reported in litres per minute
|
Estimated to be between 90 and 145 minutes
|
Rate of carbon dioxide production
Time Frame: Estimated to be between 90 and 145 minutes
|
Rate of carbon dioxide production during treadmill running.
Measured using indirect calorimetry and reported in litres per minute.
|
Estimated to be between 90 and 145 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
October 14, 2018
Primary Completion (Actual)
March 20, 2019
Study Completion (Actual)
April 16, 2019
Study Registration Dates
First Submitted
November 19, 2018
First Submitted That Met QC Criteria
November 20, 2018
First Posted (Actual)
November 21, 2018
Study Record Updates
Last Update Posted (Actual)
November 1, 2019
Last Update Submitted That Met QC Criteria
October 31, 2019
Last Verified
March 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- 18/SW/0177
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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