Clients of the Centre Interlude Bien-être, where a week of fasting is done voluntarily Not Applicable
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Informed consent 2. Participating in a fasting week at the Centre Interlude Bien-être 3. Age = 20 years, = 70 years
Exclusion criteria
Exclusion criteria: 1. Diabetes mellitus or taking glucose-lowering medication 2. BMI <18kg/m2 3. Known eating disorders (orthorexia, anorexia, bulimia) 4. Known metabolic pathologies that contraindicate fasting (e.g. deficiencies gluconeogenesis) 5. Pregnant women or during the lactation period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plasma LDL cholesterol (laboratory analysis in mmol/l) measured at the onset of fasting and two months after the beginning of the fasting week, in the group selected for blood sampling | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Total cholesterol (mmol/l), HDL cholesterol (mmol/l), triglycerides (mmol/l), blood glucose (mmol/l), CRP (mg/l) and IGF-1 (ng/ml), in the group selected for blood sampling (laboratory analysis), and variation in BMI (kg/m2), CA (cm), TA (mmHg), heart rate (/min), temperature (°C), measured at the beginning of the fast and 2 months after 2. The same measures (and LDL cholesterol) at the beginning and at the end of the fast 3. Fat-free mass measured by bioelectrical impedance analysis at 50 kHz with Nutrigard MS performed at the beginning, end and 2 months after the beginning of the fast | — |
Countries
Switzerland