Viewing Study NCT05976633



Ignite Creation Date: 2024-05-06 @ 7:20 PM
Last Modification Date: 2024-10-26 @ 3:05 PM
Study NCT ID: NCT05976633
Status: COMPLETED
Last Update Posted: 2024-03-18
First Post: 2023-07-17

Brief Title: Glycemic Response to Wild Rice and Wild Rice Blends in Humans Study
Sponsor: University of Manitoba
Organization: University of Manitoba

Study Overview

Official Title: Evaluating the Factors That Influence Glycemic Response to Wild Rice and Wild Rice Blends in Humans EFGW Study
Status: COMPLETED
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: EFGW
Brief 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 25 hours each
come to each visit fasted for at least 10-12 hours
complete a Motivation to Eat VAS following each blood measure
Detailed 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 Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None