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Dietary Fiber
Cereal with Beta Glucan for Healthy Subjects
N/A
Waitlist Available
Led By Thomas Wolever, DM, PhD
Research Sponsored by Société des Produits Nestlé (SPN)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up glucose will be measured over 2 hours postprandially (timepoints: -5, 0, 15, 30, 45, 60, 90, and 120 minutes)
Awards & highlights
Study Summary
This trial will test whether 1.4g of either oat or barley beta-glucan can significantly reduce postprandial glycemic response compared to no beta-glucan.
Who is the study for?
This trial is for non-pregnant, non-lactating individuals aged 20-65 with a BMI of 18.0 to 29.9 kg/m² and normal fasting glucose levels. Participants should be nonsmokers, willing to follow the study protocol, abstain from certain activities before study days, and provide informed consent. They must not have had major medical events recently or plan COVID-19 vaccination during the study.Check my eligibility
What is being tested?
The trial tests if cereals enriched with lower amounts of β-glucan (1.4-1.5g) from barley or oats can significantly reduce blood sugar spikes after eating compared to regular cereal without β-glucan in healthy adults.See study design
What are the potential side effects?
Since the intervention involves dietary fiber enrichment in cereals, side effects may include digestive changes such as bloating or gas but are generally expected to be minimal given that β-glucan is a natural component found in common foods.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ glucose will be measured over 2 hours postprandially (timepoints: -5, 0, 15, 30, 45, 60, 90, and 120 minutes)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~glucose will be measured over 2 hours postprandially (timepoints: -5, 0, 15, 30, 45, 60, 90, and 120 minutes)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Postprandial Glucose Incremental Area under the Curve (iAUC) from 0-2 hours
Secondary outcome measures
Glucose
Gmax
Imax
+6 moreTrial Design
3Treatment groups
Experimental Treatment
Placebo Group
Group I: OBG CerealExperimental Treatment1 Intervention
A portion of cereal (25g available carbohydrate) that contains approximately 1.4g of oat beta-glucan (OBG)
Group II: BBG CerealExperimental Treatment1 Intervention
A portion of cereal (25g available carbohydrate) that contains approximately 1.4g of barley beta-glucan (BBG)
Group III: Control CerealPlacebo Group1 Intervention
A portion of cereal (25g available carbohydrate) that contains no beta-glucan
Find a Location
Who is running the clinical trial?
INQUIS Clinical Research Ltd.Industry Sponsor
7 Previous Clinical Trials
253 Total Patients Enrolled
Société des Produits Nestlé (SPN)Lead Sponsor
337 Previous Clinical Trials
62,519 Total Patients Enrolled
INQUIS Clinical ResearchIndustry Sponsor
9 Previous Clinical Trials
283 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have a history of significant health issues.I am not on medications that affect sugar levels or are considered unsafe.I have recently changed the doses of my medications or supplements.I have not had cancer, except for non-melanoma skin cancer, in the last 2 years.I am between 20 and 65 years old and not pregnant or breastfeeding.I have not had a major injury or health issue in the last 3 months.
Research Study Groups:
This trial has the following groups:- Group 1: Control Cereal
- Group 2: OBG Cereal
- Group 3: BBG Cereal
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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