- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06242015
Ordered Eating and Acute Exercise
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
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Patrick Wilson, PhD
- Phone Number: 757-683-4783
- Email: pbwilson@odu.edu
Study Locations
-
-
Virginia
-
Norfolk, Virginia, United States, 23529
- Recruiting
- ODU Human Performance Laboratory
-
Contact:
- Patrick Wilson
- Phone Number: 757-683-4783
- Email: pbwilson@odu.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Sponsor
Investigators
- Principal Investigator: Patrick Wilson, Old Dominion University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 24-003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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