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

NCT ID: NCT05145998

Last Updated: 2021-12-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

19 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-05-23

Study Completion Date

2020-02-29

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Type2 Diabetes Mellitus Metabolic Syndrome

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Glycemic response Glucose Type 2 diabetes Legumes Metabolic Syndrome

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

5 x 5 crossover study with 4 treatments and one control
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Control - Glucola

Glucola control beverage

Group Type ACTIVE_COMPARATOR

Glucola

Intervention Type DIETARY_SUPPLEMENT

50 grams of Glucola sugar beverage

Whole peas

Whole cooked peas in a 50 gram carbohydrate meal dose

Group Type EXPERIMENTAL

Whole pea meal

Intervention Type DIETARY_SUPPLEMENT

Whole cooked peas with spaghetti sauce and a slice of bread.

Pea Flour

Pea flour in a 50 gram carbohydrate meal dose

Group Type EXPERIMENTAL

Pea flour meal

Intervention Type DIETARY_SUPPLEMENT

Pea flour with spaghetti sauce and a slice of bread.

Whole lentils

Whole cooked lentils in a 50 gram carbohydrate meal dose

Group Type EXPERIMENTAL

Whole lentils

Intervention Type DIETARY_SUPPLEMENT

Whole cooked lentils with spaghetti sauce and a slice of bread.

Lentil flour

Lentil flour in a 50 gram carbohydrate meal dose

Group Type EXPERIMENTAL

Lentil flour

Intervention Type DIETARY_SUPPLEMENT

Lentil flour with spaghetti sauce and a slice of bread.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Glucola

50 grams of Glucola sugar beverage

Intervention Type DIETARY_SUPPLEMENT

Whole pea meal

Whole cooked peas with spaghetti sauce and a slice of bread.

Intervention Type DIETARY_SUPPLEMENT

Pea flour meal

Pea flour with spaghetti sauce and a slice of bread.

Intervention Type DIETARY_SUPPLEMENT

Whole lentils

Whole cooked lentils with spaghetti sauce and a slice of bread.

Intervention Type DIETARY_SUPPLEMENT

Lentil flour

Lentil flour with spaghetti sauce and a slice of bread.

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

24 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

USA Dry Pea & Lentil Council

UNKNOWN

Sponsor Role collaborator

Iowa State University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Donna Winham

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Donna Winham, DrPH

Role: PRINCIPAL_INVESTIGATOR

Iowa State University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Iowa State University, Food Science and Human Nutrition Department

Ames, Iowa, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

17-191

Identifier Type: -

Identifier Source: org_study_id