F20-F29 F30-F39 F40-F48 F50-F59 F60-F69 F90-F98 F99
Conditions
Interventions
Group 1: The Intervention Group (IG)
is granted access to the online intervention ProTransition right after the baseline screening. The participants will complete 15 Modules and have unrestricted access to the toolkits. Meanwhile, they c
will have access to the unguided version of ProTransition after t(2) (10 weeks after randomization). In addition, participants have unlimited access to standardized medical care (TAU).
*All participa
Sponsors
Universität Ulm
Eligibility
Sex/Gender
All
Age
17 Years to 25 Years
Inclusion criteria
Inclusion criteria: Participants must: - have a treatment history of for a psychiatric disorder(s) - not have transitioned to an adult mental healthcare service - be diagnosed with at least one of the following ICD diagnoses: F2, F3, F4, F5, F6, and F9 - have enough internet access and possess a smartphone or a tablet/ laptop/ PC - have a basic knowledge of the German language, - give their informed consent to participate in the study
Exclusion criteria
Exclusion criteria: Participants will not be considered eligible for the study if they: - lack the necessary cognitive and/or attentional skills to participate in the online intervention and the assessments.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Feasibility: Sociodemographic data, Drop-out rate Client Satisfaction Questionnaire; CSF-8 Working Alliance Inventory (WAI-SF) Acceptance of psychological interventions (APOI) Negative Effects Questionnaire (NEQ) | — |
Secondary
| Measure | Time frame |
|---|---|
| Potential Effectiveness: Self-Management Self-Test (SMST) Mental Health Self Efficacy Scale (MHSES) Transition Readiness and Appropriateness Measure (TRAM-Barriers to functioning subscale) Patient Health Questionnaire (PHQ-8) Generalized Anxiety Disorder (GAD-7) Well-Being Index (WHO-5) Potential Mediators and Moderators: Brief COPE Cognitive Emotion Regulation Questionnaire (CERQ)- Blaming Others Subscale Internalized stigma of mental illness scale (ISMI) Chapman Social Anhedonia Scale Negative Effects of Relationships Scale (NERS) Measurement Points: t(0): Baseline t(1): 5 weeks after randomisation t(2): 10 weeks after randomisation (The primary measurement point to test the potential effectiveness) t(3): 15 weeks after randomisation t(4): 20 weeks after randomisation | — |
Countries
Germany
Contacts
Public ContactAyca;Fiona Ilgaz;Orban
Abteilung für Klinische Psychologie und Psychotherapie, Institut für Psychologie und Pädagogik, Universität Ulm;Abteilung für Klinische Psychologie und Psychotherapie, Institut für Psychologie und Pädagogik, Universität Ulm
Outcome results
None listed