Carbohydrate Feeding Frequency, Muscle Glycogen and Exercise Capacity in Runners

NCT ID: NCT03749785

Last Updated: 2019-11-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

7 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-10-14

Study Completion Date

2019-04-16

Brief Summary

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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

Detailed Description

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Conditions

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Exercise

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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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

Group Type ACTIVE_COMPARATOR

Regular carbohydrate feeding

Intervention Type OTHER

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

Single carbohydrate bolus

Ingestion of 75 g sucrose, given in a single bolus after 75 minutes of exercise, during a time to exhaustion run

Group Type ACTIVE_COMPARATOR

Single carbohydrate bolus

Intervention Type OTHER

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

Interventions

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Regular carbohydrate feeding

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

Intervention Type OTHER

Single carbohydrate bolus

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

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of Bath

OTHER

Sponsor Role lead

Responsible Party

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James Betts

Professor, Department for Health

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Department for Health, University of Bath

Bath, , United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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18/SW/0177

Identifier Type: -

Identifier Source: org_study_id

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