Prevention and therapy of lifestyle-dependent disease
Conditions
Interventions
Group 1: Intervention in Healthy participants: restriction of the daily intake of solid food to 8-9 hours is carried out for a period of three months.
Group 2: Intervention in patients with any compon
Sponsors
Institut für Allgemeinmedizin, Universität Ulm
Eligibility
Sex/Gender
All
Age
18 Years to 67 Years
Inclusion criteria
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
Exclusion criteria: Contraindications for fasting
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| 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. | — |
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Germany
Contacts
Public ContactDorothea Kesztyüs
Institut für Allgemeinmedizin, Universität Ulm
Outcome results
None listed