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
Group Intervention Description The Friends program The Friends program Youth 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
Name Time Method 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
Name Time Method 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 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
Trial Locations
- Locations (1)
Fjell municipality
🇳🇴Bergen, Norway