Acceptance of fibre-enriched products: Freisinger Fibre Intervention Study
Not Applicable
- Conditions
- metabolic syndrome
- Registration Number
- DRKS00013058
- Lead Sponsor
- ehrstuhl für Ernährungsmedizin der Technischen Universität München
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 115
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
- lack of declaration of consent
- current intervention study participation
- pregnancy
- current desease
- symptomatic intolerance (Gluten, Laktose, Fruktose)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method primary endpoint is to reduce the riskfactors for metabolic syndrome (measurements after 4 weeks and after 12 weeks intervention):<br>- Reduction of waist circumference (tape measure)<br>- Decrease of blood preasure (blood preasure monitor)<br>- Decrease of blood-triglycerol (blood sampling, laboratory test)<br>- Increase of blood HDL-Cholesterol (blood sampling, laboratory test)<br>- Decrease of blood glucoselevel (blood sampling, laboratory test)
- Secondary Outcome Measures
Name Time Method Secondary outcome will be measured after 4 weeks and after 12 weeks intervention:<br>- Acceptance of fiber-enriched products (questionnaires)<br>- Less energy intake by consumption of fiber-entriched products (dietary questionnaires)<br>- Changes in the microbiome (16S-sequencing)