Obesity (various ICDs)
Conditions
Interventions
Group 1: Application of the interdisciplinary, holistic, science-based program HAPpEN in obesity prevention and therapy within the existing guidelines
Group 2: Comparative data from population-based s
Sponsors
Universität Bayreuth
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: - Voluntary and written consent to use the parameters collected in primary care over a period of 12 months - Confirmed diagnosis of obesity or overweight at the time of recruitment (BMI = 30 kg/m²) - Sufficient knowledge of German - Motivation to use a digital self-observation diary
Exclusion criteria
Exclusion criteria: - State of inability to bear stress, e.g. after a serious surgical intervention - Patients with urgency for serious surgical intervention - Patients with convulsions or seizure disorders - Dementia/cognitive deficit that conflicts with the application example - Psychiatric illness that conflicts with the application example - Participation in another study (up to one month before the survey period) - Heart failure from NYHA III - Uncontrollable arterial hypertension - Severe pulmonary comorbidity (severe asthma, COPD, mMRC >2/ CAT >10, pulmonary fibrosis) - Serious psychiatric eating disorders - Other serious illness that makes physical exertion impossible
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoints include BMI, body weight, waist circumference, heart rate, blood pressure, and metabolic parameters. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include quality of life, well-being and disease burden, as well as nutritional competence, physical activity and health, social interaction and digital therapy support. | — |
Countries
Germany
Contacts
Public ContactReiner Hofmann
Universität Bayreuth
Outcome results
None listed