F32 F33 F34
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Indication for participation in the study is a diagnosis of "depressive disorder" according to ICD-10 (F32.x Depressive Episode, F33.x Recurrent depressive disorder and F34.x Persistent affective disorder), regardless of severity, diagnosed by the doctor on the respective station (only patients of the Division I and II) and regardless of whether a single or a recurrent episode is present. A further condition is a value from the BDI greater 18th.
Exclusion criteria
Exclusion criteria: Exclusion criteria are Orthopaedic, neurological or cardiovascular problems that preclude physical stress and make the processing of the test methods employed impossible. Furthermore, patients are excluded with acute psychotic symptoms from study participation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary target variables: the habitual physical activity is defined as the primary endpoint. We expect that these more highly correlated with the depression as the objective parameters. Questionnaire habitual physical activity (PCA) by Wagner & Singer, 2003: The questionnaire is to all 3 Measurement times (t0 enrollment, t1 after 4 weeks, t2 two months after completion of hospitalization) applied. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome variables: The secondary target variables are the physiological parameters of aerobic endurance and general physical fitness, depressive symptoms, HRQL and the quality of attention. - Test: 2 Km Walking Test after Bos, 2001 and Motor basic diagnostic (MBK) to Wydra, 2000: - Questionnaire: Beck Depression Inventory Audit (BDI-II) after Wintjen & Petermann, 2010: - Questionnaire: Short Form Health Questionnaire (SF-36) according to Bullinger & Kirchberger 1998: - Questionnaire: Mindful Attention Awareness Scale (MAAS) by Brown and Ryan 2003: All tests and questionnaires to all 3 Measurement times (t0 enrollment, t1 after 4 weeks, t2 two months after completion of hospitalization) applied. | — |
Countries
Germany
Contacts
LVR-Klinik Köln