Time-Restricted Feeding for the Prevention and Therapy of Lifestyle-dependent Disease
Not Applicable
- Conditions
- Prevention and therapy of lifestyle-dependent disease
- Registration Number
- DRKS00015057
- Lead Sponsor
- Institut für Allgemeinmedizin, Universität Ulm
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 104
Inclusion Criteria
Arm 1: Employees of the University/University Hospital Ulm, no known metabolic diseases, no known eating disorders.
Arm 2: Patients of the GP's practice with characteristics of metabolic syndrome without eating disorders, no insulin-dependent diabetes, no hyperthyroidism
Exclusion Criteria
Contraindications for fasting
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome measure is the achievement of the target period of 8-9 hours of food intake (recorded in a diary: time of first and last meal). For this purpose, the percentage of days with the achievement of the target over the entire study period is calculated for each participant.
- Secondary Outcome Measures
Name Time Method Secondary outcome measures are longitudinal changes in anthropometric parameters (height, weight, waist circumference) and laboratory parameters (fasting glucose, IGF-1, triglycerides, cholesterol, HDL, LDL, cortisol, LDH, CRP) as well as health-related quality of life (VAS from EQ-5D), sleep duration and quality. These data are collected at the two measurement points before and after the intervention.