Additional Study for High-Risk Groups in the Child and Youth Welfare System Within the Main Study 'Res@t: Resource-Enhancing Training for Adolescents with Media-Related Disorders and Their Parents'
Not Applicable
- Conditions
- ICD-11 6C51/6C5Y Gaming disorder/other digital-media-associated disorders
- Registration Number
- DRKS00033379
- Lead Sponsor
- niversitätsklinikum Hamburg-Eppendorf
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 32
Inclusion Criteria
receipt of child or youth welfare
- cut-off for disordered or hazardous media use in GADIS-A/-P, SOMEDIS-A/-P, or STREDIS-A/P is reached
- fulfilled criteria for pathological or hazardous media use according to ICD-11 criteria (6C51, GC5Y, QE22, QE2Y)
Exclusion Criteria
- acute severe psychiatric disorders with a symptom burden that prevents participation in the study (i. e. psychotic disorders or disorders due to substance use)
- pervasive developmental disorders (i. e. autism spectrum disorder)
- acute suicidality
- inability to understand the study instructions (i. e. severe disorders of speech or language, intelligence or lack of german language skills)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is the difference in change in the severity of MBS within 20 weeks after enrolment. It is assumed that the group using the App shows bigger decreases in MBS compared to the TAU group. In case an individual shows more than one MBS, severity will be operationalized with the most severe kind of MBS (Gaming, Social Media or Streaming). This is assessed using the following questionnaires: Gaming Disorder Scale for Adolescents/Parents (GADIS-A/-P), Social Media Use Disorder Scale for Adolescents/Parents (SOMEDIS-A/-P) and Streaming Disorder Scale for Adolescents/Parents (STREDIS-A/-P). The data is collected at 5-week intervals at 5 measurement points: Baseline, mid-training (+5 weeks), end of training (+10 weeks), catamnesis 1 (+15 weeks) and catamnesis 2 (+20 weeks). Due to the high-risk sample, the measurement times were set more closely in comparison to the main study.
- Secondary Outcome Measures
Name Time Method