Skip to content

The Effects of Beta-glucan Enriched Oatcake Consumption on Metabolic Disease Risk Factors

An Investigation of the Effects of Consuming Oatcakes Containing 4g of Oat Beta-glucan on Physiological Parameters in Individuals at Risk of Developing Metabolic Syndrome

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02615444
Enrollment
90
Registered
2015-11-26
Start date
2015-10-31
Completion date
2016-12-31
Last updated
2016-09-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Metabolic Syndrome X

Keywords

Metabolic Syndrome X, Overweight, Waist Circumference, Blood Pressure, Cholesterol, Oat beta glucan

Brief summary

The purpose of this study is to determine whether daily consumption of soluble fibre, oat beta glucan (4g), for six weeks will have any impact on overweight/obese individuals in terms of risk factors used to define metabolic disease.

Detailed description

The purpose of this study is to determine whether daily consumption oat beta glucan (4g) for six weeks will have any impact on overweight/obese individuals in terms of risk factors used to define metabolic disease. Oat beta-glucan has been incorporated into a novel oatcake product manufactured by Nairn's Oatcakes Ltd. Consumption of the oatcake products will deliver enough oat-beta glucan to the diet to meet European Food Safety Authority health claims for lowering blood cholesterol and reducing post-prandial glycaemic responses.

Interventions

DIETARY_SUPPLEMENTBeta-glucan enriched oatcake

5 oatcakes enriched with oat beta-glucan will be consumed daily for six weeks

DIETARY_SUPPLEMENTIsocaloric control

6.5 wheat based control snacks without beta-glucan will be consumed daily for six weeks

Sponsors

Queen Margaret University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Males and females 18 years and older * Waist circumference measurements of ≥94cm for males and 80cm for females, or a body mass index of ≥30kg/m2 * Individuals who are able to provide informed consent

Exclusion criteria

* Postmenopausal females * Smokers * Individuals who suffer from, or taking medication for, cardiovascular or gastro-intestinal disease * Impaired glucose tolerance/Diabetes mellitus * Pregnancy or breastfeeding * Those who have high dietary fibre intakes (\>20g/day) * Known food allergies to oats, wheat, lactose, or sesame seeds

Design outcomes

Primary

MeasureTime frame
Waist Circumference6 weeks

Secondary

MeasureTime frame
Fasting Serum Triglycerides6 weeks
Oral Glucose Tolerance Test6 weeks
Fasting Serum HDL Cholesterol6 Weeks
Blood Pressure6 Weeks
Interleukin-66 weeks
Energy Intakes (kilocalories) and Macronutrient intakes (grams) from food diaries6 weeks
Fasting Serum total Cholesterol6 weeks

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026