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FRIENDS as an Indicative Prevention Program in Norway

The FRIENDS-program as Indicative Prevention for Children and Adolescents With Symptoms of Anxiety and Depression

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01802424
Enrollment
80
Registered
2013-03-01
Start date
2012-02-29
Completion date
2014-12-31
Last updated
2015-12-07

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

Conditions

Anxiety

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

NORCE Norwegian Research Centre AS
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 15 Years
Healthy volunteers
No

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

MeasureTime 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

MeasureTime frame
Changes in life-quality (measured by KINDL)from baseline to 12 months after completing the FRIENDS programWhen 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 programWhen 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 programWhen completing the intervention and 3months and 12 months after having completed the intervention

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026