F32.2 F41.1
Conditions
Interventions
Group 1: The participating subjects are assigned to control or intervention group in random order after checking inclusion and exclusion criteria. The interventions take place in a group setting as pa
Sponsors
Psychiatrische Klinik Charité Berlin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with a mental illness from the group of affective illnesses, anxiety disorders as well as psychotic illnesses and personality disorders.
Exclusion criteria
Exclusion criteria: Suicidality, acute danger to oneself or others, severe psychotic experiences or severe physical illness that contradicts participation in the intervention.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint should be the subjects' psychovegetative activation in the form of a measurement of the activity of the pituitary-hypothalamus-adrenal system (“stress axis”) and the activation of the sympathetic nervous system. In particular, the parameters salivary cortisol and salivary amylase are to be measured and the heart rate variability will be examined. The measurements will be taken immediately before and after the intervention/control-condition. | — |
Secondary
| Measure | Time frame |
|---|---|
| Subjectively perceived anxiety and stress symptoms before and after the intervention are to be measured using standardized questionnaires - the State-Trait-Anxiety-Depression-Inventory (Laux et al., 2016), the State-Trait-Anxiety-Inventory (Spielberger et al., 2001) and the Positive Mental Health Scale (Lukat et al ., 2016). The measurements will be taken immediately before and after the intervention/control-condition. | — |
Countries
Germany
Contacts
Public ContactAnna Brabeck
Charité Berlin Klinik für Psychiatrie und Psychotherapie
Outcome results
None listed