Predictors of Clinical Course and Treatment Response in DBT Programmes
Sponsor: Oslo University Hospital • ClinicalTrials.gov ID: NCT04318899
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The project is a collaboration between The National Centre for Suicide Research and Prevention (NSSF) and clinical units with Dialectical Behaviour Therapy (DBT) programmes. A methodological and technological platform has been established that enables clinicians to deliver high quality treatments over extended periods of time, to evaluate their own performance and productivity and to report it in a uniform and systematic way that will enable comparison across clinical settings and programmes. The collected data constitute the basis for conducting the clinical study with the overall aim to study predictors of the clinical course and treatment response in patients admitted to DBT programmes in Norway.
Interventions
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Dialectical Behaviour Therapy adapted for adolescents (DBT-A)
(Behavioral)
DBT developed by Marsha Linehan (Linehan 1993a; 1993b) and adapted for adolescents (DBT-A) by Miller, Rathus \& Linehan, 2007 consisting of 20 weeks of weekly individual therapy (60 minutes), multifamily skills training (120 minutes), family therapy sessions as needed and telephone coaching outside therapy sessions.
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Dialectical Behaviour Therapy - Standard version (DBT)
(Behavioral)
DBT developed by Marsha Linehan (Linehan 1993a, 1993 b) consisting of 1 weekly session of individual therapy (60 minutes), 1 weekly session of skills training (120 minutes), and telephone coaching with individual therapists outside therapy sessions as needed.
Eligibility criteria
Conditions
Locations
- Søndre Oslo DPS/Oslo Universitetssykehus HF — Oslo, Oslo, Norway
- Moss DPS/Østfold sykehus HF — Moss, Norway
- Psykiatrisk senter ytre Helgeland/Helgelandssykehuset HF — Sandnessjøen, Norway
- Bjerketun behandlingshjem/Vestreviken HF — Sandvika, Norway
- BUP Lian/St Olavs Hospital HF — Trondheim, Norway
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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