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Glycemic Response to Wild Rice and Wild Rice Blends in Humans Study — EFGW  

Blood Glucose Clinical Trial

Official title:
Evaluating the Factors That Influence Glycemic Response to Wild Rice and Wild Rice Blends in Humans (EFGW) Study.

Clinical Trial Summary

The goal of this clinical trial is to test the effects of wild rice and wild rice blends compared to other rice on glycemic control and evaluating factors that influence glycemic response to wild rice in healthy individuals. The main questions aim to answer: 1. Is there an effect of wild rice on blends on glycemic control and response? 2. Does cooking wild rice via stovetop or microwave change its glycemic response? 3. Is the wild rice blend product palatable? 4. What is the subjective appetite when consuming the treatment? Participants will: - consent to attend 5 study visits being 2.5 hours each - come to each visit fasted for at least 10-12 hours. - complete a Motivation to Eat VAS following each blood measure

Clinical Trial Description

This study will be a crossover randomized trial consisting of 5 sessions. The wild rice products will be provided by the Myera group. Participants will fast and arrive at the Richardson Centre for Food Technology and Research (RCFTR) between 7am - 11am on the session day. They will be provided either of the study treatments based on randomization sequence. Baseline blood glucose (0 min) will be measured twice via finger stick blood sample right before their first bite of the study product, and at 15, 30, 45, 60, 90 and 120 mins after baseline in duplicate. VAS will be completed following consumption of the treatments to measure palatability and subjective appetite at baseline (0 min), and at 15, 30, 45, 60, 90, and 120 minute time points. The primary objective is to test the effects of wild rice and wild rice blends compared to other rice on glycemic control and evaluating factors that influence glycemic response to wild rice in humans performed via the finger stick blood glucose that will be measured throughout each session as outlined above. Secondly, to test whether wild rice glycemic response is affected based on cooking method. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05976633
Study type Interventional
Source University of Manitoba
Contact
Status Completed
Phase N/A
Start date July 14, 2023
Completion date February 29, 2024
View Details
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