Anxiety
Conditions
Keywords
Open trial, Indicative prevention, Youth anxiety, Cognitive behavioral therapy
Brief summary
The purpose of this pilot-study is to evaluate a cognitive behavioral program, the Friends-program, as indicated prevention for anxious youth. The youths are recruited by school nurses who will also lead the intervention groups applying the Friends-manual.
Interventions
The Friends program is a ten weeks group interventions based on principles from Cognitive Behavioural Therapy aimed at ameliorating symptoms of anxiety and depression in children and adolescents. There are age-specific versions of the manual, one for children 8-12 years and one for adolescents 12-15 years.
Sponsors
Study design
Eligibility
Inclusion criteria
* subclinical to clinical symptoms of anxiety with or without comorbid symptoms of depression
Exclusion criteria
* previously diagnosed with conduct disorder, major life-crises that needs to be attended to, serious school refusal, Obsessive Compulsive Disorder, mental retardation or autism.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in anxiety symptoms from baseline to 12 months after completing the FRIENDS program, measured by the Spence Children Anxiety Scale (SCAS) | When completing the intervention and 3months and 12 months after having completed the intervention |
Secondary
| Measure | Time frame |
|---|---|
| Changes in life-quality (measured by KINDL)from baseline to 12 months after completing the FRIENDS program | When completing the intervention and 3months and 12 months after having completed the intervention |
| Changes in depressive symptoms (measured by the Short Mood and Feeling questionnaire)from baseline to 12 months after completing the FRIENDS program | When completing the intervention and 3months and 12 months after having completed the intervention |
| Changes in psychosocial functioning (measured by the Strengths and difficulties questionnaire)from baseline until 12 months after having completed the FRIENDS program | When completing the intervention and 3months and 12 months after having completed the intervention |
Countries
Norway