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Evaluation of the online community Between The Lines

Evaluation of the online community Between The Lines - BTL Online Community

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00038611
Enrollment
164
Registered
2025-12-09
Start date
2026-02-02
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

The study is aimed at children, adolescents, and young adults without a necessary clinical diagnosis. Participation is possible regardless of whether a mental illness is present. However, the study focuses on individuals with psychological stressors, such as stress, worries, or stressful situations, regardless of a formal diagnosis.

Interventions

Group 1: Intervention group: Access to the online community “Between The Lines,” a digital platform for psychosocial support for children, adolescents, and young adults (aged 12–21) for a period of 12

Sponsors

Klinische Psychologie, Institut für Experimentelle Psychologie Heinrich-Heine-Universität Düsseldorf
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 21 Years

Inclusion criteria

Inclusion criteria: - Confident use of smartphone/tablet/computer - Stable internet access - Informed consent - Sufficient knowledge of German - Participants in the intervention group: confirmation of community rules during the onboarding process (required for access to the online community)

Exclusion criteria

Exclusion criteria: - Acute suicidality (suicide item > 1 in the Beck Depression Inventory (BDI), a standardized, self-reported screening instrument) - Children and adolescents aged 22 years - If their consent or that of their legal guardians is lacking. - Children and adolescents who are in an acute mental health crisis at the time of recruitment that requires immediate therapeutic intervention. - Non-acceptance of the community rules (leads to exclusion from the intervention condition; participants may remain in the control group)

Design outcomes

Primary

MeasureTime frame
Psychosocial well-being (WHO-5 questionnaire): baseline, 6 and 12 weeks, follow-up 24 weeks Stress experience (PSS-10 questionnaire): baseline, 6 and 12 weeks, follow-up 24 weeks Perceived social support (F-SozU-K 14 questionnaire): baseline, 6 and 12 weeks, follow-up 24 weeks Perceived stigmatization (STIG-9 questionnaire): baseline, 6 and 12 weeks, follow-up 24 weeks

Countries

Germany

Contacts

Public ContactSusanne Becker

Klinische Psychologie, Institut für Experimentelle Psychologie Heinrich-Heine-Universität Düsseldorf

sbecker@hhu.de+49 211 81 14722

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026