Comparison of Behavioral Activation and Antidepressant Medication in the Treatment of Adolescents With Depression

Stopped early · Not applicable

Conditions studied: Major Depressive Disorder

In brief

This study focuses on treating adolescents with depression. The study has two main purposes. The first is to compare a new form of therapy for depression called Behavioral Activation (BA) to the antidepressant medication fluoxetine. BA therapy helps depressed people get more involved in activities they find enjoyable, which can reduce symptoms of depression. Research shows that both BA and fluoxetine work to reduce depressive symptoms in adolescents. However, unlike previous research, this study examines how well the two treatment options work in comparison to each other. Participants in the study are randomized to receive treatment with either BA or fluoxetine for 18 weeks. The second aim of the study is to examine the brain functions of adolescents in both treatment groups. Participants undergo functional Magnetic Resonance Imaging (fMRI) scans before and after treatment. The data from these scans will be used to compare the brains of participants in the BA condition with those in the fluoxetine condition. Also, the scans may show possible differences between participants' brains before and after treatment. These data may help scientists determine the ideal form of depression treatment for different types of people.

Key facts

Study ID

NCT01740726

Run by

Emory University

People needed

3

Starts

2013-01-01

Expected to finish

2014-03-01

Last updated by the study team

2017-12-20

Who can join

Age: 13 and older, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and female adolescents ages 13-17
• Current diagnosis of Major Depressive Disorder as determined by the Kiddie Schedule for Affective Disorders and Schizophrenia (KSADS-PL), Children's Depression Rating Scale (CDRS-R) raw score > 45 (T-score > 65) at baseline
• Estimated full scale IQ > 80 as determined by the Wechsler Intelligence Scale for Children (WISC)
• Able to receive outpatient care
• Willing to discontinue other psychosocial treatments
• Not taking psychotropic medications in the one month prior to consent, with the exception of psychostimulant medication prescribed for the treatment of attention-deficit/hyperactivity disorder (ADHD)

You may not qualify if…

• Current or past diagnosis of bipolar, schizophrenia, schizophreniform, schizoaffective disorders, or psychosis not otherwise specified
• Current diagnosis of developmental disorder, severe conduct disorder, life-threatening anorexia, obsessive-compulsive disorder, or autism-spectrum disorders
• Taking psychotropic medications prior to entry
• Estimated IQ < 80
• Alcohol/drug dependence or abuse within the last 3 months
• Potential/confirmed neurological disorder or epilepsy
• Claustrophobia
• Presence of a medical condition that precludes fMRI
• Endorsement of imminent and serious suicidality
• Medical conditions for which treatment with fluoxetine is contraindicated or that take precedence over the presence of major depressive disorder (MDD)
• Pregnancy

Where it is running

• Emory Executive Park — Atlanta, Georgia, United States

Full record on ClinicalTrials.gov

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