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Metabolic Effects of Pulse Consumption on Biomarkers in Adults With Type 2 Diabetes or Met Syn

Not Applicable
Completed
Conditions
Metabolic Syndrome
Type2 Diabetes Mellitus
Interventions
Dietary Supplement: Lentil flour
Dietary Supplement: Whole pea meal
Dietary Supplement: Pea flour meal
Dietary Supplement: Whole lentils
Dietary Supplement: Glucola
Registration Number
NCT05145998
Lead Sponsor
Iowa State University
Brief Summary

The purpose of this study is to determine glycemic response of four different meals containing either whole green peas, whole lentils, powdered green peas, or powdered lentils in comparison to Glucola. Participants are adults with type 2 diabetes mellitus or metabolic syndrome.

Detailed Description

The 5 test treatments (Glucola, whole green peas, green pea flour, whole lentils, and lentil flour) will be administered randomly over five weeks. The test Participants will be required to consume the entire test treatment meal in 12 minutes while being observed. Venous blood samples will be collected for blood glucose and insulin levels at time 0 (fasting) and at 30, 60, 90, 120, and 180 minutes post-treatment (timing of the post-treatment blood draws started at time 0 \[post-treatment\], which is when the participant finishes consuming the treatment meal). During the first visit blood was drawn for a lipid panel and HbA1C values. Thyroid stimulating hormone (TSH) and complete blood count (CBC) values were analyzed during the second visit, and vitamin D levels analyzed during the final visit. Blood analysis was completed by a reputable biomarker diagnostics laboratory, Quest Diagnostics. Anthropometric measures such as weight, height, waist circumference, and blood pressure were collected at screening and at the start of each test day. Thirteen hours before testing, participants consumed a standardized frozen meal to reduce the potential variation in glycemic responses on test day due to varying pre-evening dietary intakes. This control meal was selected by each participant before the start of the study. Each participant was provided the same frozen meal every time, since the subjects serve as their own controls. The day before test day, participants completed a 24 hour food recall, satiety, and gastrointestinal questionnaires. The morning of each test day participants completed the International Physical Activity Questionnaire (IPAQ), satiety, and gastrointestinal questionnaires. Test meal and blood glucose results at the 5 test points were entered into SPSS statistical software (V. 25) for data cleaning and analysis. Physical activity and the 24 hour dietary recall data were used to classify individuals on activity and dietary quality. Satiety responses were compared against each of the 5 test meals for each participant as well as the gastrointestinal responses using SPSS.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
19
Inclusion Criteria
  • Age 24-70 years
  • BMI between 22-40
  • Medical diagnosis of type 2 diabetes
  • HbA1C <10%)
  • OR have 3+ indicators of metabolic syndrome (high triglycerides, low HDL-cholesterol, high blood pressure) plus prediabetes HbA1c.
Exclusion Criteria
  • Uncontrolled hypertension or other health issues, e.g., gastrointestinal disease
  • Weight changes of >10% of participants body weight within a 6 month period
  • Pregnant or breastfeeding
  • Allergy to peas, lentils, tomatoes, gluten, or latex
  • HgbA1c level of >10% at screening
  • Unwillingness or inability to follow study protocol.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Lentil flourLentil flourLentil flour in a 50 gram carbohydrate meal dose
Whole peasWhole pea mealWhole cooked peas in a 50 gram carbohydrate meal dose
Pea FlourPea flour mealPea flour in a 50 gram carbohydrate meal dose
Whole lentilsWhole lentilsWhole cooked lentils in a 50 gram carbohydrate meal dose
Control - GlucolaGlucolaGlucola control beverage
Primary Outcome Measures
NameTimeMethod
Change in baseline blood glucose over 3 hours (glycemic response)Time 0 (fasting) then every 30 minutes for 3 hours

Venous blood samples were collected via venous catheter. Whole blood samples were analyzed for glucose content and insulin at Quest Diagnostics.

Secondary Outcome Measures
NameTimeMethod
Change in gastrointestinal symptoms3 hours postprandial, and 12 hours postprandial

Gastrointestinal concerns and changes were noted on a descriptive questionnaire

Change in satiety sensationTime 0 (fasting) then every 30 minutes for 3 hours

Satiety level measured using a visual analog scale (0-100) every 30 minutes postprandially. A higher score indicates greater satiety.

Trial Locations

Locations (1)

Iowa State University, Food Science and Human Nutrition Department

🇺🇸

Ames, Iowa, United States

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