metabolic syndrome
Conditions
Interventions
Group 1: Intervention with 10g fiber in food per day. Stratification with yes/no of gender and metabolic syndrome.
Group 2: Placebogroup: food contains no fiber (study duration: 12 weeks). Stratificat
Sponsors
Lehrstuhl für Ernährungsmedizin der Technischen Universität München
Eligibility
Sex/Gender
All
Age
40 Years to 65 Years
Inclusion criteria
Inclusion criteria: - middle aged Cohort enable central project - 40-65 years old - written declaration of consent - waist circumference women > 88 cm and > men 102 cm (for the persons with metabolic risk) - 50% men, 50% women - Caucasian
Exclusion criteria
Exclusion criteria: - lack of declaration of consent - current intervention study participation - pregnancy - current desease - symptomatic intolerance (Gluten, Laktose, Fruktose)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| primary endpoint is to reduce the riskfactors for metabolic syndrome (measurements after 4 weeks and after 12 weeks intervention): - Reduction of waist circumference (tape measure) - Decrease of blood preasure (blood preasure monitor) - Decrease of blood-triglycerol (blood sampling, laboratory test) - Increase of blood HDL-Cholesterol (blood sampling, laboratory test) - Decrease of blood glucoselevel (blood sampling, laboratory test) | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome will be measured after 4 weeks and after 12 weeks intervention: - Acceptance of fiber-enriched products (questionnaires) - Less energy intake by consumption of fiber-entriched products (dietary questionnaires) - Changes in the microbiome (16S-sequencing) | — |
Countries
Germany
Contacts
Public ContactRachel Rennekamp
Technische Universität München, Lehrstuhl für Ernährungsmedizin, enable Stundienzentrum
Outcome results
None listed