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Effects of Lentil Consumption on Post-prandial Blood Glucose and Insulin

The Love of Lentils (LoL) Study: The Effects of Acute Consumption of Common Lentil Varieties on Post-prandial Blood Glucose and Insulin Levels in Healthy Adult

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02426606
Enrollment
48
Registered
2015-04-27
Start date
2014-11-30
Completion date
2016-02-29
Last updated
2016-10-25

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

Conditions

Healthy

Keywords

Lentils, Post-prandial, Glycemic response, Insulin response, Diabetes, Mixed meal, Glycemia, Slowly digestible starch, Post-prandial glycemia

Brief summary

The purpose of this study is to assess the effects of consuming various lentil varieties in mixed-meals (containing either white rice or white potato) on post-prandial blood glucose and insulin as compared to white rice or white potato alone.

Detailed description

Eligible participants will undergo a total of 6 study visits. During each visit, a fasted blood sample will be taken by fingerprick, and approximately 500µL of blood will be dripped into a collection tube. The participant will then consume a meal of either: white bread, white rice (or white potato), or white rice with lentils (or white potato with lentils). White bread will be consumed on the first study visit and the rest of the meals will take place in random order in the visits following. Each meal will provide a total of 50g available carbohydrate. Six more blood samples will be taken by fingerprick at 15, 30, 45, 60, 90 and 120 minutes after the beginning of the meal.

Interventions

OTHERVarious lentil varieties (varying in slow digested starch content)

Randomized, cross-over block design. Comparison of glycemic and insulinemic responses following meals composed of: * white rice or white rice combined with 1 of 3 different lentil varieties or * white potato or white potato combined with 1 of 3 different lentil varieties Participants with be assigned to either the white rice or white potato group. Meals will provide 50g available carbohydrate (AC). In meals containing lentils, whole cooked lentils will provide 25g AC either white rice or white potato will provide 25g AC. Meals will be randomly consumed across 6 study visits, with 2 white bread control meals (one of which will take place on the first visit).

Sponsors

Agriculture and Agri-Food Canada
CollaboratorOTHER_GOV
Pulse Canada
CollaboratorOTHER
Saskatchewan Pulse Growers
CollaboratorOTHER
University of Guelph
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy men and women * Age 18-40 years * BMI 20-30 kg/m2

Exclusion criteria

* Tobacco use * Pregnant or breastfeeding * Fasting blood glucose ≥ 7.0 mmol/L * Any major medical condition including a history of AIDS or hepatitis * Medical or surgical event requiring hospitalization within 3 months of randomization * Any medications except a stable dose (3 months) of oral contraceptives, blood pressure or statin medications * Blood pressure \>140/90 mm Hg * Natural health products (NHPs) used for glycemic control * Probiotic supplements * Dietary fibre supplements * Consumption of \>4 servings of pulses per week * Food allergy or non-food life threatening allergy * Shift workers * Alcohol consumption \>14 drinks/week or \>4 drinks/sitting * Recent or intended significant weight loss or gain (\>4 kg in previous 3 months) * Elite athletes

Design outcomes

Primary

MeasureTime frameDescription
Postprandial blood glucoseAcute- 2 hours following mealDifferent meals will be consumed on separate occasions over 3-6 week period.
Postprandial blood insulinAcute- 2 hours following mealDifferent meals will be consumed on separate occasions over 3-6 week period.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026