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FRIENDS as an Indicative Prevention Program in Norway

Not Applicable
Completed
Conditions
Anxiety
Interventions
Behavioral: The Friends program
Registration Number
NCT01802424
Lead Sponsor
NORCE Norwegian Research Centre AS
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
The Friends programThe Friends programYouth with increased levels of anxiety are thought to regulate their fear by recognizing bodily cues, learning relaxation, regulating thoughts and feelings and expose themselves to situations and objects that activate their anxiety.
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
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
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

Trial Locations

Locations (1)

Fjell municipality

🇳🇴

Bergen, Norway

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