E11.9 I51.6
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - participants either suffer from pre-diabetes, type 2 diabetes or are at high risk of developing diabetes (FINDRISK°>11) and/or cardiovascular diseases (being overweight/obese, being affected by hypertension, elevated blood lipid- and glucose levels, unfavourable nutrition habits, physical inactivity and smoking); - persons 18 years of age and older; - persons who are physically and mentally able to participate in the study; - written informed consent.
Exclusion criteria
Exclusion criteria: -persons with severe acute or chronic diseases who are not able to participate in the study at the discretion of their treating physician; -minors under the age of 18 years.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intervention group: -Body weight at baseline, after 8 weeks and after 6 and 12 months, compared to controls; -Blood glucose values at baseline, after 8 weeks and after 6 and 12 months, compared to controls; -Long-term improvement of the diabetes risk (risk score FINDRISK) at baseline and after 12 months, compared to controls. | — |
Secondary
| Measure | Time frame |
|---|---|
| Intervention group: blood lipids, body mass index,waist circumference, systolic and diastolic blood pressure, eating habits (questionnaire, 3-day food log), level of physical activity (questionnaire), mental wellbeing (wellbeing questionnaire), health-related quality of life (SF-12) and self-efficacy (questionnaire) at baseline, after 8 weeks and after 6 and 12 months, compared to controls. | — |
Countries
Germany
Contacts
Vinzenzkrankenhaus Hannover