E78 E11 I10
Conditions
Interventions
Group 1: intervention group:
Lifestyle intervention program: 1 coaching session on the individual health situation, 12 seminar units in 12 weeks, followed by monthly seminars, total duration 1 year
G
Sponsors
FH Münster
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: The study will include adults (> 18 years) who are mentally and linguistically capable of fulfilling the study requirements. Written informed consent must be obtained before the start of the study. For the analysis of the cortisol concentration, only participants with a hair length of at least 3 cm at the back of the head can be included.
Exclusion criteria
Exclusion criteria: Patients suffering from a serious acute or chronic illness according to their own statement or at the discretion of the attending physician and who cannot reasonably be expected to participate will be excluded from the study. Subjects suffering from hypercortisolism (e.g. Cushing's disease) or being treated or substituted with glucocorticoids will also be excluded from the cortisol concentration study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| body weight (kg) measurement time points: baseline (t0), after 8 weeks (t1), after 6 months (t2), after 12 months (t3) | — |
Secondary
| Measure | Time frame |
|---|---|
| Anthropometric parameters: Waist circumference Vital signs: systolic and diastolic blood pressure, resting pulse Clinical parameters: Lipids (total cholesterol, triglycerides), fasting glucose, HbA1c (%), cortisol concentration in scalp hair Questionnaires: perceived stress level, dietary behavior, physical activity, social-cognitive variables, mindful eating behavior, mindfulness assessment measurement time points: baseline (t0), after 8 weeks (t1), after 6 months (t2), after 12 months (t3) | — |
Countries
Germany
Contacts
Public ContactHeike Englert
FH Münster
Outcome results
None listed