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

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

      • Bath, United Kingdom, BA2 7AY
        • Department for Health, University of Bath

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
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
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
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.

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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