Skip to content

Second Meal Effects of a Wholegrain Cereal Product on Blood Glucose Response

Second Meal Effects of a Wholegrain Cereal Product on Blood Glucose Response

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05291806
Enrollment
17
Registered
2022-03-23
Start date
2022-03-17
Completion date
2022-06-13
Last updated
2022-07-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Glucose Response

Brief summary

The aim of this study is to investigate second meal effects of a wholegrain cereal product on blood glucose response. The wholegrain cereal product will be consumed in the evening and blood glucose analyzed after a standardized breakfast meal the following morning.

Interventions

OTHERReference Product

This intervention is based on white rice.

OTHERWholegrain product Dose A

This wholegrain intervention contains whole cereal kernels.

OTHERWholegrain product Dose B

This wholegrain intervention contains whole cereal kernels.

OTHERWholegrain product Dose A, cut kernels

This wholegrain intervention contains cut cereal kernels.

Sponsors

Aventure AB
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
35 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. Male or Female, 35 to 65 years of age 2. BMI 18.5-29.9 kg/m2 3. Agree to maintain consistent dietary habits and physical activity levels for the duration of the study. 4. Healthy as determined by medical history and information provided by the volunteer. 5. Willingness to complete questionnaires and follow instructions associated with the study and to complete all visits. 6. Has given voluntary, written, informed consent to participate in the study.

Exclusion criteria

1. Elevated fasting blood glucose (above 6.1 mmol/L at fasting on visit 1, 2, 3 or 4) 2. Women who are pregnant or breast feeding 3. Any medical condition(s) or medication(s) known to significantly affect glucose metabolism. Significance to be assessed by the QI 4. Use of medication, over-the-counter medication, natural health products or dietary supplements/probiotics that may affect glucose metabolism is prohibited during this study. Significance to be assessed by the QI. Participants who are taking allowed prescribed medications must agree to maintain their current method and dosing regimen during the course of the study unless other is recommended by their physician. 5. Known Type I or Type II diabetes, including women who previously have had gestational diabetes. 6. Use of antibiotics within 2 weeks of enrollment 7. Metabolic diseases and/or chronic gastrointestinal diseases (IBS, Crohns etc.) 8. Allergy to ingredients included in investigational product, reference, or standardized meal 9. Participants restricted to a vegetarian or vegan diet 10. Intolerance to gluten 11. Individuals who are averse to venous catheterization or capillary blood sampling 12. Currently active smokers (or using other tobacco products, and e-cigarettes) 13. Unstable medical conditions as determined by QI 14. Participation in other clinical research trials 15. Individuals who are cognitively impaired and/or who are unable to give informed consent 16. Acute infection 17. Any other condition which in the QI's opinion may adversely affect the individual's ability to complete the study or its measures or which may pose significant risk to the individual \-

Design outcomes

Primary

MeasureTime frameDescription
Postprandial capillary blood glucose iAUC (0-120 min)Outcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in capillary blood glucose between wholegrain products and reference in the total incremental area under the curve iAUC(0-120 min) after the standardized breakfast meal.

Secondary

MeasureTime frameDescription
Fasting capillary blood glucoseOutcome measures will be assessed just before the standardized meal is consumed.The change in fasting capillary blood glucose the morning after consuming either wholegrain products or reference.
Postprandial capillary blood glucose iAUC (0-60 min)Outcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in capillary blood glucose between wholegrain products and reference in the 1-hour incremental area under the curve iAUC(0-60 min) after the standardized breakfast meal.
Postprandial capillary blood glucose 2-hour iPeak(0-120 min) (incremental maximum value)Outcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in capillary blood glucose between wholegrain products and reference in the 2-hour iPeak(0-120 min) (incremental maximum value) after the breakfast meal.
Postprandial Insulin iAUC(0-120 min)Outcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in venous blood insulin between wholegrain products and reference in the total incremental area under the curve iAUC(0-120 min) after the standardized breakfast meal.
Postprandial Insulin CmaxOutcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in venous blood insulin between wholegrain products and reference in Cmax after the standardized breakfast meal.
Postprandial Insulin TmaxOutcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in venous blood insulin between wholegrain products and reference in Tmax after the standardized breakfast meal.
Fasting InsulinOutcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in fasting venous blood insulin the morning after consuming either wholegrain products or reference.
Postprandial insulin iAUC (0-60 min)Outcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in venous blood insulin between wholegrain products and reference in the 1-hour incremental area under the curve iAUC(0-60 min) after the standardized breakfast meal.
Postprandial venous blood insulin 2-hour iPeak(0-120 min) (incremental maximum value)Outcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in venous blood insulin between wholegrain products and reference in the 2-hour iPeak(0-120 min) (incremental maximum value) after the breakfast meal.
Postprandial capillary blood glucose CmaxOutcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in capillary blood glucose between wholegrain products and reference in 2-hour Cmax(0-120 min) (maximum concentration) after the breakfast meal.
Postprandial capillary blood glucose TmaxOutcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in capillary blood glucose between wholegrain products and reference in 2-hour Tmax(0-120 min) (the time to maximum concentration) after the breakfast meal.

Other

MeasureTime frameDescription
GLP-1 iAUC(0-60 min)Outcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in GLP-1 between wholegrain products and reference in the1-hour incremental area under the curve iAUC(0-60 min) after the standardized breakfast meal.
GLP-1 CmaxOutcome measures will be assessed just before and immediately after the standardized meal is consumed.The changein GLP-1 between wholegrain products and reference in Cmax after the standardized breakfast meal.
GLP-1 TmaxOutcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in GLP-1 between wholegrain products and reference in Tmax after the standardized breakfast meal.
Fasting PYYOutcome measures will be assessed just before the standardized meal is consumed.The change in fasting PYY the morning after consuming either wholegrain products or reference.
PYY 2-hour mean concentrationOutcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in PYY between the wholegrain products and the reference in the 2-hour mean concentration after the breakfast meal.
PYY 1-hour mean concentrationOutcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in PYY between the wholegrain products and the reference in the 1-hour mean concentration after the breakfast meal.
Fasting GLP-1Outcome measures will be assessed just before the standardized meal is consumed.The change in fasting GLP-1 the morning after consuming either wholegrain products or reference.
GLP-1 iAUC(0-120 min)Outcome measures will be assessed just before and immediately after the standardized meal is consumed.The change in GLP-1 between wholegrain products and reference in the total incremental area under the curve iAUC(0-120 min) after the standardized breakfast meal.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026