Ordered Eating and Acute Exercise

April 1, 2024 updated by: Patrick Wilson, PhD, Old Dominion University

The Effect of Ordered Eating on Postprandial Glucose and Substrate Utilization During an Acute Exercise Bout

There is well documented evidence that ingesting dietary carbohydrate in large amounts tends to increase postprandial glucose. In healthy populations, this is not necessarily a problem, but continuous exposure to high levels of glucose-hyperglycemia-is a defining characteristic and risk factor for type 2 diabetes mellitus. Consuming a carbohydrate-rich food as the final food in a meal sequence has been shown to significantly reduce postprandial glucose excursions in both diabetes patients and in healthy controls. The exact mechanisms behind this phenomenon are not well understood, but one proposed course is simply that the vegetable and protein already being digested slows the rate of glucose rise.

Despite the findings, little-to-no research has examined how manipulating the order of foods in a meal impacts subsequent exercise responses. In this experimental crossover study, each participant will undergo two acute feeding conditions (carbohydrate-rich foods first vs. last in a meal), which will be followed by exercise 60 minutes later. We will observe the effects of meal order on postprandial glucose, substrate/fuel utilization, and subjective perceptions at rest and during 30 minutes of exercise.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

30

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 Contact

Study Locations

    • Virginia
      • Norfolk, Virginia, United States, 23529
        • Recruiting
        • ODU Human Performance Laboratory
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Currently physically active (scheduled exercise at least three days per week for 30 minutes each time over the last three months)
  • Ability to perform moderate-to-high intensity running for at least 30 minutes

Exclusion Criteria:

  • Any allergy or other condition that would prohibit the consumption of poultry, rice, or broccoli
  • Any injury or disease (cardiovascular disease, diabetes, pulmonary disease except controlled asthma) precluding physical exercise
  • Currently pregnant
  • Implanted electrical devices such as a pacemaker.

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Carbohydrate-first meal
Rice (150 grams) eaten first, followed by broccoli (150 grams) and chicken (100 grams)
Experimental: Carbohydrate-last meal
Broccoli (150 grams) and chicken (100 grams) eaten first, followed by rice (150 grams)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postprandial glucose
Time Frame: 2 hours (premeal and 30, 60, 90, and 120 minutes after eating)
Blood glucose will be measured with fingerstick samples and a portable glucometer
2 hours (premeal and 30, 60, 90, and 120 minutes after eating)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Carbohydrate use
Time Frame: 100 minutes (premeal and continuously for 90 minutes after eating)
Carbohydrate utilization will be estimated from respiratory gas exchange
100 minutes (premeal and continuously for 90 minutes after eating)
Fat use
Time Frame: 100 minutes (premeal and continuously for 90 minutes after eating)
fat utilization will be estimated from respiratory gas exchange
100 minutes (premeal and continuously for 90 minutes after eating)
Hunger-satiety perceptions
Time Frame: 2 hours (Premeal and at 15, 30, 45, 60, 68, 78, 88, 120 minutes after eating)
Hunger, appetite, satiety, and fullness on a 0-10 Likert scale
2 hours (Premeal and at 15, 30, 45, 60, 68, 78, 88, 120 minutes after eating)
Rating of perceived exertion
Time Frame: 30 minutes (at 8, 18, 28 minutes of exercise)
Rating of effort during 30-minute exercise bout
30 minutes (at 8, 18, 28 minutes of exercise)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Patrick Wilson, Old Dominion University

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)

February 6, 2024

Primary Completion (Estimated)

July 30, 2025

Study Completion (Estimated)

July 30, 2025

Study Registration Dates

First Submitted

January 28, 2024

First Submitted That Met QC Criteria

January 28, 2024

First Posted (Actual)

February 5, 2024

Study Record Updates

Last Update Posted (Actual)

April 3, 2024

Last Update Submitted That Met QC Criteria

April 1, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 24-003

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-identified IPD will be shared upon reasonable request. Requests should be made to the corresponding author.

IPD Sharing Time Frame

The data will be made available upon the study's publication and will remain available for at least 5 years

IPD Sharing Access Criteria

Researchers with a justified reason for wanting access to the data

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.

Clinical Trials on Glucose Metabolism Disorders

Clinical Trials on Carbohydrate-first meal

3
Subscribe