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CompletedNCT06763562Updated Oct 16, 2026

Food Orders on Blood Glucose and Fuel Use at Rest

An interventional study of Carbohydrate-first meal and Carbohydrate-last meal in Glucose Metabolism Disorders, Hunger and Fat Burn, sponsored by Old Dominion University. Completed at 1 site in United States. Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-16.

Sponsored by Old Dominion University · Not applicable, Interventional, and Basic science

Updated Oct 16, 2026Now CompletedPrimary completion moved+2 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Consuming a carbohydrate-rich food as the final food in a meal, as compared to the first food in a meal, has been shown to reduce blood glucose levels after eating in both diabetes patients and in healthy controls. However, gaps remain in the literature in this area of research, and currently little is known about how substrate (fuel) use is impacted by altering food order. In addition, most studies to date have used a mix of meat and plant foods, while little research has focused exclusively on vegetarian foods. This randomized experiment will examine how altering the order of foods eaten in a vegetarian meal impacts blood glucose and fuel utilization at rest.

02

Conditions studied

  • Glucose Metabolism Disorders
  • Hunger
  • Fat Burn
03

In context

Glucose Metabolism Disorders

361 studies on the registry are indexed under Glucose Metabolism Disorders; 38 are open to participants now.

This study's enrollment of 50 is below the median of 60 across 308 interventional studies indexed under Glucose Metabolism Disorders.

Browse Glucose Metabolism Disorders studies →

Lead sponsor

Old Dominion University is the lead sponsor of 27 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 18-70 years old
  • Free from any allergy or condition that precluding consumption of edamame, butter, and rice
  • Not currently pregnant
  • Free of any medical conditions requiring the use of insulin
  • Have no history of bariatric surgery
  • Have no implanted electrical devices such as a pacemaker

Exclusion criteria

Exclusion Criteria:

  • Younger than 18 and older than 70 years old
  • Having an allergy or condition that precludes consumption of edamame, butter, and rice
  • Currently pregnant
  • Any medical conditions requiring the use of insulin
  • A history of bariatric surgery
  • Having an implanted electrical device such as a pacemaker
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (actual)

Study arms

  • Experimental
    Carbohydrate-first meal

    Other: Carbohydrate-first meal

  • Experimental
    Carbohydrate-last meal

    Other: Carbohydrate-last meal

Interventions

  • OtherCarbohydrate-first meal

    Rice eaten first (150 grams), followed by edamame (150 grams) and butter (10 grams)

  • OtherCarbohydrate-last meal

    Edamame (150 grams) and butter (10 grams) eaten first, followed by rice (150 grams)

06

What researchers measure

Primary outcomes

  1. Respiratory exchange ratio

    Ratio of carbon dioxide production and oxygen consumption for determination of fuel use

    Time frame: 90 minutes (baseline/premeal and at 30, 60, and 90 minutes postmeal)

Secondary outcomes

  1. Fat use

    Fat utilization will be estimated from respiratory gas exchange

    Time frame: 90 minutes (baseline/premeal and at 30, 60, and 90 minutes postmeal)

  2. Carbohydrate use

    Carbohydrate utilization will be estimated from respiratory gas exchange

    Time frame: 90 minutes (baseline/premeal and at 30, 60, and 90 minutes postmeal)

  3. Blood glucose

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

    Time frame: 90 minutes (baseline/premeal and 30, 60, and 90 minutes postmeal)

  4. Hunger-satiety perceptions

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

    Time frame: 90 minutes (baseline/premeal and 30, 60, and 90 minutes postmeal)

07

Study locations

1 site
  • Old Dominion University Human Performance Laboratory
    Norfolk, Virginia 23529, United States
08

References and documents

Individual participant data

Plan to share: Yes — De-identified IPD will be shared as supplementary material associated with the published peer-reviewed publication or through a publicly available repository (depending on the journal's preference).

Time frame: Data will become available once the associated article is officially published. The data will be made available indefinitely.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Recruiting→Completed
changed Oct 16, 2026
Primary completion
Jun 30, 2026→Nov 26, 2025 (actual)
Oct 16, 2026
Study completion
Jun 30, 2026→Nov 26, 2025 (actual)
Oct 16, 2026
Enrollment
60 (estimated)→50 (actual)
Oct 16, 2026
Show all 1 update
  1. Oct 16, 2026
    Recruiting→Completed
    Primary completion Jun 30, 2026→Nov 26, 2025 (now actual)
    Study completion Jun 30, 2026→Nov 26, 2025 (now actual)
    Enrollment 60 (estimated)→50 (actual)
    + 6 other changes: identifiers, verification date, oversight details, contact details, site details and index terms

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT06763562
Lead sponsor
Old Dominion University
Responsible party
Patrick Wilson, PhD (Associate Professor of Exercise Science, Old Dominion University) — Principal investigator
First posted
Jan 8, 2025
Start date
Jan 5, 2025
Primary completion
Nov 26, 2025
Completion
Nov 26, 2025
Last update
Oct 16, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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