EICHORCondition: Anxiety Disorders · Sponsor: Helse Stavanger HF
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The goal of this feasibility study is to test whether a new blended digital intervention for adolescents with anxiety disorders is feasible and acceptable for use, and to help plan future larger scale studies. The main questions it aims to answer are: * A: Can the investigators recruit appropriate participants? * B: How appropriate are the data collection procedures and outcome measures? * C: Are the study procedures and interventions suitable for and acceptable to the participants? * D: Does the research team have the resources and ability to manage the study and intervention? * E: Does the intervention show promise of being successful for adolescents with anxiety disorders? Participants will: * Receive outpatient anxiety treatment, typically every other week or weekly. * Use the Sidekick app as a homework supplement to plan, carry out, and evaluate exposure exercises between treatment sessions. * Complete questionnaires before, during, after, and three months after using the app. * Some participants and therapists will be invited to take part in qualitative interviews following the intervention.
This description comes directly from the study's public registry record.
Pia R Hauge, Master · +47 92877830 · pia.rygg.hauge@sus.no
Aleksander H Erga, PhD · +4751515684 · aleksander.hagen.erga@sus.no
There is no obligation to join — the study team can answer your questions about taking part.
Always discuss trial participation with your own doctor first.
Inclusion Criteria: * 13 to 18 years old * Adequate Norwegian reading, writing and speaking skills * Access to the internett and a smart-phone * Diagnosed anxiety disorder * Receiving outpatient treatment for their anxiety disorder * Exposure therapy included in therapy during the study period * Therapist agrees to incorporate the app as an ad-on to therapy * For patients receiving medication, inclusion requires a stable dose of medication for a psychiatric disorder for six weeks Exclusion Criteria: * Participants with serious mental illness, such as suicidality or poor general functioning may be excluded if participation is considered unfeasible or potentially harmful. Decision will be based on collaborative evaluation by the participants therapist and the research-team.
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| Children and Adolescent Mental Health Outpatient Clinics | Stavanger, Norway | Recruiting |
| Stavanger Universitetssykehus | Stavanger, Norway | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT07145307