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The Chewing study: The effects of chewing duration on blood glucose levels

The Chewing study: The effects of chewing duration on blood glucose levels - The Chewing study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON50095
Enrollment
26
Registered
2020-10-01
Start date
2020-10-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

gezonde voedselkeuze healthy food choice

Interventions

Test subjects will consume two testlunches (rice and chickenpeas) in duplicate following a short and long chewing protocol.

Sponsors

Wageningen UR; Stichting DLO
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: * Apparently healthy men and women (based on questionnaire, self-reported) * Aged between 18 * 55 yrs * BMI between 18.5 and 30

Exclusion criteria

Exclusion criteria: Participants will be excluded if: * Employed by the FHCR group of Wageningen Food & Biobased Research. * BMI > 30.0 en =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/week * Having food allergies * Participation in another clinical trial at the same time * Gastric emptying disorder. * Problems with chewing and/or swallowing

Design outcomes

Primary

MeasureTime frame
Primaire study parameter is bloodglucose levels during the 3-hours following a test lunch consumed following a long/short chewing protocol. Blood glucose parameters are: time-to-peak, maximum value and area under the curve.

Secondary

MeasureTime frame
Secondary study parameters are salivary amylase and particle sizes of the food boli at the moment of swallowing.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)