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Acute Effects of Dietary Fiber on Blood Glucose and Satiety Considering the Dose–Response Relationship – A Randomized Controlled Intervention Study

Acute Effects of Dietary Fiber on Blood Glucose and Satiety Considering the Dose–Response Relationship – A Randomized Controlled Intervention Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00039384
Enrollment
20
Registered
2026-06-11
Start date
2026-06-02
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

The study investigates the rise in blood glucose following sugar intake and its potential modulation by dietary fiber. Pronounced or repeatedly elevated postprandial blood glucose levels are considered a risk factor for the development of metabolic diseases such as type 2 diabetes. The aim of the study is to improve the understanding of preventive nutritional strategies and to examine whether different amounts of dietary fiber contribute to stabilizing blood glucose levels.

Interventions

Group 1: Intake of water without chia seeds, followed by a standard oral glucose tolerance test (75 g glucose). Group 2: Single intake of 10 g chia seeds dissolved in water prior to the oral glucose t

Sponsors

Universitätsklinikum Frankfurt am Main
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Eligible for inclusion are adults (= 18 years) in good general health without known metabolic disorders and with a body mass index between 18.5 and 29.9 kg/m². Participants must be willing to attend all scheduled study visits and provide written informed consent after receiving appropriate information about the study. Adequate German language proficiency is required to ensure full understanding of the study information and questionnaires.

Exclusion criteria

Exclusion criteria: Individuals with known metabolic disorders, particularly diabetes mellitus or impaired glucose tolerance, as well as chronic diseases affecting glucose metabolism or digestion, are excluded from participation. Persons taking medications that influence glucose metabolism, those with known allergies or intolerances to chia seeds or components of the test solutions, pregnant or breastfeeding women, and individuals with acute illnesses at the time of assessment are also excluded from the study.

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the postprandial glucose response, defined as the area under the glucose curve (AUC0–120) within 120 minutes following an oral glucose tolerance test, measured using continuous glucose monitoring (CGM) and capillary blood glucose measurements.

Secondary

MeasureTime frame
Secondary endpoints include the maximum postprandial glucose concentration and the time to peak within the 120-minute period, subjective satiety, well-being, and gastrointestinal symptoms (assessed using standardized self-report measures), as well as diurnal and nocturnal interstitial glucose profiles during the test days.

Countries

Germany

Contacts

Public ContactTobias Engeroff

Institut für Arbeitsmedizin, Sozialmedizin und Umweltmedizin

engeroff@sport.uni-frankfurt.de+49 (0)69 798 24543

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 29, 2026