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Clinical Trials in Norway / NCT07346911
Starting soon Not applicable

Digital Interventions for Relapse Prevention in Adolescence

NCT07346911 · tracked via the Priya Life Science Norway tracker
Phase
Not applicable
Started
2026-04-07
Last updated
2026-03-13

Condition(s) studied

Major Depression DisorderANXIETY DISORDERS (or Anxiety and Phobic Neuroses)

Investigational drug(s) / intervention(s)

Transdiagnostic app interventionTransdiagnostic mastery course

Transdiagnostic app intervention: A transdiagnostic, self-guided CBT app, called TankeVirus (literally translated Thought Viruses), consisting of three components: 1. Standardized self-assessment for mental health: 'Test your psychological immune system'. 2. Educational mini-series: A 30-minute, entertaining video series that teaches users to build resilience by addressing essential needs like sleep (psychological immune system), recognizing negative thought patterns (thought viruses), and developing healthier coping mechanisms (psychological vitamins). 3. Daily practice: Over 20 days, users receive a short, 1-2-minute video each morning. These videos provide practical tips, small experiments, or simple tasks designed to help users integrate healthier coping strategies into their daily lives.

Transdiagnostic mastery course: Group-based webinar offering psychoeducation based on principles of CBT.

Study summary

Some adolescents experience periods of anxiety and/or depression, and some find that these periods return over time. The purpose of this study is to examine whether digital interventions-where individuals work systematically with their own thoughts and feelings during periods when they feel well-can help them maintain well-being for longer.

The study includes adolescents aged 16-19 who have previously experienced episodes of depression and/or anxiety to a degree that led them to seek help (e.g., from a school nurse, general practitioner, health clinic, or child and adolescent mental health service). Through a research app on their smartphones, participants complete tasks and answer questionnaires. The study is fully digital. Some participants meet with a therapist in digital group sessions, while others work independently with the digital content.

We will also examine the cost-benefit aspects of offering such interventions. If the study achieves its goals, digital interventions may eventually become a service offered to adolescents recovering from depression and anxiety.

Eligibility

Sex
ALL
Min age
16 Years
Max age
19 Years
Healthy volunteers
No
Inclusion Criteria: * Currently in full or partial remission for a minimum of 2 months from a depressive disorder or an anxiety disorder as defined by self-reported scores on RCADS-47: previous episode(s) of t-score \> 65 and current t-score =\<65. * Native or fluent Scandinavian language skills. * Willingness to take part even when allocated to the non-preferred arm of the trial. Exclusion Criteria: * Ongoing depressive disorder, ongoing anxiety disorder as defined by current t-score =\<65 on RCADS-47. * Recent completion of one of the interventions in the two interventional arms. * no available smartphone.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Oslo Oslo Norway

More University of Oslo trials in Norway

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07346911 on ClinicalTrials.gov ↗ ← All trials in Norway