Cephalic Phase Responses to Nutritive and Non-Nutritive Sweeteners

Not Applicable

Active, not recruiting

• Conditions: Pre Diabetes
• Interventions: Other: No Oral Stimulation; Other: Oral water stimulation; Other: Oral Sucralose Stimulation; Other: Oral Salt Stimulation; Other: Oral Sucrose stimulation

• Registration Number: NCT06387316
• Lead Sponsor: Purdue University

Brief Summary

This study will focus on changes in blood sugar in response to tasting different types of sweeteners using continuous glucose monitoring (CGM) technology.

Detailed Description

Participants will be recruited through posting of advertisements about the study. Flyers will be posted on and off campus. Individuals interested in the study will contact the researchers and an initial appointment will be scheduled.

First Lab Visit (Day 1):

Consent and Instruction: Researchers will explain the study procedures, including the use of continuous glucose monitoring (CGM), home-based taste testing and wearing the Fitbit activity tracker. Participants will complete a short questionnaire (screening questionnaire) that elicits demographic, health and activity information. Participants can choose to decline to answer any questions they prefer not to answer. Researchers will determine if participants meet eligibility criteria and participants will then decide if they want to participate. A CGM device will be placed on the participant's arm to monitor glucose levels continuously. Placing the monitor involves putting an egg-shaped plastic container (about the size of a golf ball) on the back of one arm and a button is pushed and this presses the sensor on the arm. It is held on by adhesive. It is like applying a band aid though there is a hair-like flexible fiber that is pressed into the skin (not into a vein). The participant feels little more than mild pressure - far less than a needle stick. Participants will be given individually portioned, labeled sample solutions including a nutritive sweetener, non-nutritive sweetener, a non-sweet control stimulus (salt) and just water along with commercially available no sodium rice cakes (cut to bite-size pieces). Participants will be instructed to place one rice cake sample in their mouth and sip a 5ml oral solution sample and masticate for 15 seconds and expectorate. This will be repeated 3 additional times. With about 15 seconds between samples. This exposure will require about 2 minutes. This will be repeated 4 times a day (before breakfast, before lunch, before dinner and at 8PM) on 8 days. There will be no oral stimulation for 2 days. Participants will be provided with activity recall sheets and instructed to record their sleep patterns, and physical activity for 10 days. This form will only contain an identification code, no personally identifiable information be on the form. Participants will also be asked to wear a Fitbit to monitor activity. This is exactly like wearing a wristwatch.

Study Timeline

• Study Start: 2024-03-26
• Study First Submitted: 2024-03-27
• Status Verified: 2024-04
• Primary Completion: 2024-04-17
• Study First Submitted QC: 2024-04-24
• Last Update Submitted: 2024-04-24
• Study First Posted: 2024-04-29
• Last Update Posted: 2024-04-29
• Study Completion: 2025-03-30

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Adults aged between 18 to 70 years old will be eligible to participate.
• Good health and without known medical conditions, including but not limited to, diabetes, cardiovascular diseases, metabolic disorders, and any other chronic conditions that could significantly affect glycemia.
• No history of major surgeries, organ transplantations, or significant medical interventions that might impact glycemia.
• No medications that could interfere with glucose metabolism or sweet taste perception. Use of vitamins or contraceptives will be permissible if continued for the 12 days of study participation.
• No dietary restrictions or sensitivities that prevent them from tasting or swishing sweeteners and rice cakes provided during the study.

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Exclusion Criteria

Not provided

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
No Oral Stimulation	No Oral Stimulation	No oral stimulation is provided.
Oral Sucrose stimulation	Oral Sucrose stimulation	Oral stimulation with sucrose.
Oral Sucrose stimulation	No Oral Stimulation	Oral stimulation with sucrose.
Oral Water Stimulation	Oral water stimulation	Oral stimulation with water.
Oral Sucralose Stimulation	Oral Sucralose Stimulation	Oral stimulation with sucralose.
Oral Salt Stimulation	Oral Salt Stimulation	Oral stimulation with salt.

Primary Outcome Measures

Name	Time	Method
Blood glucose concentration	10 days	blood glucose concentration measured by continuous glucose monitoring

Trial Locations

Locations (1)

Purdue University; 🇺🇸 West Lafayette, Indiana, United States