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The Effect of Chewing Duration on Blood Glucose Levels

The Effect of Chewing Duration on Blood Glucose Levels

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04648397
Enrollment
26
Registered
2020-12-01
Start date
2020-11-16
Completion date
2020-11-27
Last updated
2021-01-20

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

Conditions

Glucose, High Blood, Glucose, Low Blood

Keywords

Chewing behaviour

Brief summary

This study aims to assess the impact of speed of consumption of two starch-based foods varying in fibre content on blood glucose levels in normal healthy subjects. Furthermore, the mediating roles of salivary amylase and particle size on blood glucose levels will be studied. The study has a randomized cross-over design. Subjects consume two test-lunches (chick peas and brown rice) in duplicate on 8 different test days, at either long or short chewing duration. Glucose responses will be monitored via a continuous glucose monitoring device and expectorated boluses will be collected during each test day for assessments of amylase activity and food particle size.

Detailed description

Research suggests that high glucose level variability and large dips in glucose levels may have a negative impact on cognitive function and self-reported wellbeing. The way food is consumed (e.g. chewing duration) may regulate blood glucose levels. The underlying mechanism that links consumption speed to metabolic responses, satiation and health is largely unknown. This study aims to assess the impact of speed of consumption of two starch-based foods varying in fibre content, on blood glucose levels in normal healthy subjects. Furthermore, the mediating roles of salivary amylase and particle size on blood glucose levels are studied. The study has a randomized cross-over design. Each subject consumes two different test-lunches (chick peas and brown rice) in duplicate at either long or short duration. Their breakfast will be standardized during these 8 test days. For a duration of 12 days, blood glucose levels will be monitored via a continuous glucose device. Furthermore expectorated boluses will be collected for assessment of amylase activity and food particle size.

Interventions

OTHERLow glycaemic load, high fibrous product

Test-lunch of 370 grams of chickpeas, seasoned with a herb- and spice mix to increase palatability. Glycaemic load 18.5. Consumed in duplicate.

OTHERHigh glycaemic load, low fibrous product

Test-lunch of 257 grams of brown rice, seasoned with rice-oil and a herb- and spice mix to increase palatability. Glycaemic load 44.9. Consumed in duplicate.

Sponsors

Wageningen University and Research
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Apparently healthy men and women (based on questionnaire, self-reported) * Aged between 18 - 55 yrs * BMI between 18.5 - 30 kg/m2 * In possession of a Smartphone running on iOS or Android

Exclusion criteria

* Diagnosed with Diabetes mellitus type 1 or 2 * Under treatment for neurological or psychiatric complaints, including eating disorders * History of gastro-intestinal surgery or having (serious) gastro-intestinal complaints * Use of medication/supplements that may influence the study results, such as medicines known to interfere with glucose homeostasis. This will be judged by our medical doctor * Following a diet or gained/lost \>=5kg weight in the previous month. * Coeliac disease or gluten intolerance * Skin allergy, eczema or known sensitivity for plasters * use of drugs * Current smokers * Using \> 14 glasses of alcohol per week * Having a food allergy for the test foods * Participation in another clinical trial at the same time * Suffering from a stomach emptying disorder * Employed by or an intern at the FHCR group of Wageningen Food & Biobased Research.

Design outcomes

Primary

MeasureTime frameDescription
Blood glucose responses in the 3 hrs following lunch12 days in total to cover all test daysmeasured by a continuous glucose monitoring device

Secondary

MeasureTime frameDescription
Particle size of food boluson 4 of the 8 test days, at day 1, day 2, day 3 and day 4 or day 5, day 6, day 7 and day 8 depending on groupmeasured in food boli of the test-lunches by image analysis
Amylase activityat day 1measured in saliva
In vitro starch digestion rates in food boluson 4 of the 8 test days, at day 1, day 2, day 3 and day 4 or day 5, day 6, day 7 and day 8 depending on groupassessed in food boli of the test-lunches by making use of INFOGEST 2.0 protocol

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026