The Treatment for Adolescents With Depression Study (TADS)
Duke Medical Center · Duke University Hospital
Abstract
To report effectiveness outcomes across 36 weeks of randomized treatment. DESIGN AND SETTING: Randomized, controlled trial conducted in 13 academic and community sites in the United States. Cognitive behavior and combination therapies were not masked, whereas administration of placebo and fluoxetine was double-blind through 12 weeks, after which treatments were unblinded. Patients assigned to placebo were treated openly after week 12, and the placebo group is not included in these analyses by design.
Three hundred twenty-seven patients aged 12 to 17 years with a primary DSM-IV diagnosis of major depressive disorder. INTERVENTIONS: All treatments were administered per protocol. MAIN OUTCOME MEASURES: The primary dependent measures rated blind to treatment status by an independent evaluator were the Children's Depression Rating Scale-Revised total score and the response rate, defined as a Clinical Global Impressions-Improvement score of much or very much improved.
Citation impact
- FWCI
- 51.27
- Percentile
- 100%
- References
- 0
Authors
11Topics & keywords
- Fluoxetine
- Placebo
- Randomized controlled trial
- Major depressive disorder
- Rating scale
- Cognitive behavioral therapy
- Depression (economics)
- Suicidal ideation
- Good health and well-being