Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
65 participants
INTERVENTIONAL
2008-03-31
2013-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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1
Group cognitive intervention (the Adolescent Coping with Stress)
the Adolescent Coping with Stress
A group cognitive intervention, manualized and highly structured. Includes 8 sessions (á 1.5 hours) and a booster session 6 months after termination of the actual intervention. Groups leaders are specifically trained for this course.
2
Treatment as usual
Treatment as usual
The usual treatment received by the adolescent with mild to moderate self-reported depressive symptoms in school health care.
3
Healthy controls, receive usual health education in school health care
usual health education
usual health education given by the school nurses, targeted for healthy controls with no depressive symptoms according to the self-report scale
Interventions
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the Adolescent Coping with Stress
A group cognitive intervention, manualized and highly structured. Includes 8 sessions (á 1.5 hours) and a booster session 6 months after termination of the actual intervention. Groups leaders are specifically trained for this course.
Treatment as usual
The usual treatment received by the adolescent with mild to moderate self-reported depressive symptoms in school health care.
usual health education
usual health education given by the school nurses, targeted for healthy controls with no depressive symptoms according to the self-report scale
Eligibility Criteria
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Inclusion Criteria
* adequate knowledge of the Finnish language
* informed consent from the adolescent (all) and his/her parent (under 15 years)
* healthy controls comprise subjects with no depressive symptoms
Exclusion Criteria
* ongoing other severe psychiatric illness precluding group participation
* mental retardation
14 Years
16 Years
ALL
No
Sponsors
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University of Helsinki
OTHER
University of Eastern Finland
OTHER
Kuopio University Hospital
OTHER
City of Vantaa
OTHER_GOV
City of Kuopio
OTHER_GOV
City of Turku
OTHER_GOV
Finnish Institute for Health and Welfare
OTHER_GOV
Responsible Party
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Linnea Karlsson
senior researcher
Principal Investigators
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Mauri J Marttunen, Professor
Role: STUDY_DIRECTOR
National Institute for Health nd Welfare, Dept of Mental Health and Substance Abuse Services
Locations
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Kuopio University Hospital and Kuopio University
Kuopio, , Finland
Turku Primary Health care and Adolescent Psychiatric clinic
Turku, , Finland
Vantaa Primary Health Care
Vantaa, , Finland
Countries
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Other Identifiers
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KTL423-0
Identifier Type: -
Identifier Source: org_study_id
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