The feasibility study of an online training for young adults transitioning from child and adolescent mental health care services to adult care: a randomized controlled trial of the ProTransition-App

Not Applicable

• Conditions: F50-F59; F60-F69; F20-F29; F30-F39; F40-F48; F90-F98; F99; Schizophrenia, schizotypal and delusional disorders; Mood [affective] disorders; Neurotic, stress-related and somatoform disorders

• Registration Number: DRKS00025486
• Lead Sponsor: niversität Ulm

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-06-02
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 47

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

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.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Feasibility: <br>Sociodemographic data, Drop-out rate<br>Client Satisfaction Questionnaire; CSF-8<br>Working Alliance Inventory (WAI-SF)<br>Acceptance of psychological interventions (APOI)<br>Negative Effects Questionnaire (NEQ)<br>

Secondary Outcome Measures

Name	Time	Method
Potential Effectiveness:<br>Self-Management Self-Test (SMST)<br>Mental Health Self Efficacy Scale (MHSES)<br>Transition Readiness and Appropriateness Measure (TRAM-Barriers to functioning subscale)<br>Patient Health Questionnaire (PHQ-8)<br>Generalized Anxiety Disorder (GAD-7)<br>Well-Being Index (WHO-5)<br><br>Potential Mediators and Moderators:<br>Brief COPE<br>Cognitive Emotion Regulation Questionnaire (CERQ)- Blaming Others Subscale<br>Internalized stigma of mental illness scale (ISMI)<br>Chapman Social Anhedonia Scale<br>Negative Effects of Relationships Scale (NERS)<br><br>Measurement Points: <br>t(0): Baseline <br>t(1): 5 weeks after randomisation <br>t(2): 10 weeks after randomisation (The primary measurement point to test the potential effectiveness)<br>t(3): 15 weeks after randomisation <br>t(4): 20 weeks after randomisation