Structured implementation of digital, systematically updated guideline recommendations for enhanced therapeutic adherence in schizophrenia.
Not Applicable
- Conditions
- F20Schizophrenia
- Registration Number
- DRKS00028895
- Lead Sponsor
- Bezirkskliniken Schwaben – Klinik für Psychiatrie, Psychotherapie und Psychosomatik der Universität Augsburg (BKH Augsburg)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 287
Inclusion Criteria
Persons of legal age (female, male, diverse) with employment at one of the 16 participating hospitals as a physician/physician or psychologist/psychologist will be included. Moreover, sufficient knowledge of German (defined by the ability to work with patients) is considered as inclusion criterion.
Exclusion Criteria
No exclusion criteria are defined.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method As a primary outcome, guideline conformity among health care providers will be assessed by means of a Questionnaire on guideline knowledge of the S3 Guideline Schizophrenia. For this purpose, 46 casuistic, i.e. case vignette oriented multiple choice questions are asked. 30 out of 46 items including correctly answered 5 cardinal questions will be operationalized as guideline-compliant and will serve as an evaluation of the effectiveness of the implementation strategies.<br>The primary outcome will be assessed six months after the start of the intervention.
- Secondary Outcome Measures
Name Time Method Secondary outcomes include digital health literacy measured by the eHealth Literacy Scale and usability of the respective formats by the System Usability Scale. We will further assess providers' confidence in decision making using the Provider Decision Process Assessment Instrument, as well as their ability in shared decision making using the Participatory Decision Making Questionnaire (PEF-FB-Doc). Furthermore, attitudes towards and use of the respective formats (traditional print format or MAGICapp) will be recorded. Secondary outcomes will be assessed six months after the start of the intervention.