Patients with a primary psychiatric diagnosis according to ICD-10/ICD-11 criteria, including schizophrenia spectrum disorders, substance-induced psychotic disorders, schizoaffective disorder, delusional disorder, unipolar depressive disorders, bipolar disorders, anxiety disorders, and related psychiatric conditions.
Conditions
Interventions
Group 1: Following written informed consent, participants will be enrolled in the study. Initially, patient data will be collected in a standardized manner, including a comprehensive characterization
Sponsors
Technische Universität München, TUM Klinikum, Rechts der Isar
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Inclusion criteria: Primary diagnosis of one of the following psychiatric disorders: schizophrenia, substance-induced psychotic disorder, schizoaffective disorder, delusional disorder, unipolar depressive disorder, bipolar disorder, or anxiety disorder, diagnosed according to ICD-10/ICD-11 criteria. Age = 18 years. Treatment on an open psychiatric ward; patients admitted under court order are excluded. Capacity to provide informed consent (decision-making capacity) and written informed consent. Sufficient language proficiency to understand study information and complete questionnaires. The patient is receiving treatment at the clinic on a voluntary basis.
Exclusion criteria
Exclusion criteria: Exclusion criteria: Physical illnesses that make participation in the study impossible (e.g., delirium, severe intoxication, severe infection, stroke). Acute suicidality. Patients admitted under court order. Severe cognitive impairment/intellectual disability that prevents valid data collection. Insufficient language proficiency despite assistance. Legal or administrative restrictions that exclude participation in research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoints of the study are the number of successfully implemented PRoGO approaches on the ward, measured by the completion of comprehensive Problem Lists and Treatment Plans, as well as the consistent application of the SOAP framework (Subjective, Objective, Assessment, Plan) in progress notes. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include the improvement in scale scores at discharge compared to baseline (admission). | — |
Countries
Germany
Contacts
Public ContactStefan Leucht
Technische Universität München, TUM Klinikum, Rechts der Isar
Outcome results
None listed