Maple Products and Exercise Performance

NCT02880124 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2019-08-21

No results posted yet for this study

Summary

The purpose of this study is to compare the acute metabolic responses and time-trial performance following the ingestion of carbohydrate solutions containing either maple syrup, maple sap, corn syrup, a commercial sport drink or water.

Conditions

  • Carbohydrate Ingestion
  • Fuel Selection
  • Athletic Performance

Interventions

DIETARY_SUPPLEMENT

Solution ingestion

Subjects will be required to ingest 2 litres of the experimental solution, spread over the 2 hours of exercise. A first ingestion of 572 mL of solution will be made at rest, 30 minutes before starting exercise, and 286 mL will be ingested immediately before the start of exercise and every 30 minutes during the exercise period.

BEHAVIORAL

Constant load cycling

Subjects will be required to perform 2 hours of cycling exercise at a power output eliciting 60% of VO2max.

PROCEDURE

Expired gas sampling

Subjects will be asked, twice, to provide a forced expiration into a 10 mL plastic tube in order to collect a sample expired gases. This procedure will be done immediately before blood sampling and ingestion of the solution, every 30 minutes.

PROCEDURE

Indirect respiratory calorimetry

A mouthpiece and nose plug will be placed on the subject and expired gases will be analyzed by a metabolic cart during 3 minutes. This procedure will be done immediately before expired gas collection, blood sampling and ingestion of the solution, every 30 minutes.

OTHER

Palatability

Subjects will be asked to fill out a short form on the palatability of the solution ingestion, after ingesting the first solution and at the end of exercise, after ingestion the last solution.

OTHER

Gastrointestinal

At the end of the time trial, subjects will be asked to fill out a short form on gastrointestinal issues they might have had during experimentation.

PROCEDURE

Blood sampling

A catheter will be inserted in an antecubital vein and a saline solution will be continuously perfused to maintain the vessel open. 15 mL of blood will be collected every 30 minutes, immediately before ingesting the solution.

BEHAVIORAL

Time trial

Subjects will be required to complete a simulated 20-km time trial on the cycle ergometer set in linear mode (where resistance is proportional to pedalling cadence), starting at 70% of the peak power output for the cadence spontaneously adopted by the subject during 2 hours of exercise.

Sponsors & Collaborators

  • Fédération des producteurs acéricoles du Québec

    collaborator UNKNOWN
  • Université de Montréal

    lead OTHER

Principal Investigators

  • Jonathan Tremblay, Ph.D. · Université de Montréal

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-07-11
Primary Completion
2017-12-22
Completion
2018-03-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02880124 on ClinicalTrials.gov