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Glucose Metabolism DisordersNCT06242015

Ordered Eating and Acute Exercise

A study testing Carbohydrate-first meal and Carbohydrate-last meal in people with Glucose Metabolism Disorders and Hunger, run by Old Dominion University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 18 to 60 yearsHealthy volunteers can take part
Conditions the study is for
Glucose Metabolism Disorders, Hunger
What is being tested?
Carbohydrate-first meal and Carbohydrate-last meal
Could I receive a placebo?
No, everyone receives an active treatment
How many people
23 participants
Where
1 siteUnited States
Study dates
6 Feb 2024to 30 Jul 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 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

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • ODU Human Performance Laboratory

    Norfolk, Virginia, 23529

Other trials in United States

About this study

Official title: 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.

Being tested
Carbohydrate-first meal, Carbohydrate-last meal
Keywords
Exercise, Glucose, Fat metabolism, Hunger
Medical subject headings
Glucose Metabolism Disorders, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Carbohydrate-first mealOther

    Rice (150 grams) eaten first, followed by broccoli (150 grams) and chicken (100 grams)

  • Carbohydrate-last mealOther

    Broccoli (150 grams) and chicken (100 grams) eaten first, followed by rice (150 grams)

Study groups in NCT06242015
Study groupRoleWhat they receive
Carbohydrate-first mealExperimentalNot described
Receives: Other: Carbohydrate-first meal
Carbohydrate-last mealExperimentalNot described
Receives: Other: Carbohydrate-last meal

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Postprandial glucose

    Blood glucose will be measured with fingerstick samples and a portable glucometer

    Measured: 2 hours (premeal and 30, 60, 90, and 120 minutes after eating)

Secondary outcomes (4)
  1. Carbohydrate use

    Carbohydrate utilization will be estimated from respiratory gas exchange

    Measured: 100 minutes (premeal and continuously for 90 minutes after eating)

  2. Fat use

    fat utilization will be estimated from respiratory gas exchange

    Measured: 100 minutes (premeal and continuously for 90 minutes after eating)

  3. Hunger-satiety perceptions

    Hunger, appetite, satiety, and fullness on a 0-10 Likert scale

    Measured: 2 hours (Premeal and at 15, 30, 45, 60, 68, 78, 88, 120 minutes after eating)

  4. Rating of perceived exertion

    Rating of effort during 30-minute exercise bout

    Measured: 30 minutes (at 8, 18, 28 minutes of exercise)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Feb 2024
  2. Study start6 Feb 2024
  3. Primary completion30 Jul 2024
  4. Study completion30 Jul 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
23 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06242015
Sponsor's protocol ID
24-003
Status last verified
Jul 2025
First submitted
28 Jan 2024
Last updated
1 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified IPD will be shared upon reasonable request. Requests should be made to the corresponding author.

Questions about this trial

What is this clinical trial studying?

A study testing Carbohydrate-first meal and Carbohydrate-last meal in people with Glucose Metabolism Disorders and Hunger, run by Old Dominion University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Postprandial glucose (time frame: 2 hours (premeal and 30, 60, 90, and 120 minutes after eating)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Aug 2025.

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