214
Participants
Start Date
December 31, 2015
Primary Completion Date
July 31, 2022
Study Completion Date
December 31, 2022
Escitalopram
Youth in the MED condition will be given the USFDA approved antidepressant, escitalopram for the treatment of depression or anxiety in youth and follow a standard dose titration schedule of 5 mg/day for 1 week, 10mg/day for 1 week, then with a target dose of 20-30 mg/day by 4 weeks. Titration will be no faster than 5mg/week. This titration guideline was drawn from the escitalopram package insert for pediatric dosing, which states that target doses may be achieved by 4 weeks.
Cognitive behavioral Psychotherapy
All participants (No MED and MED) will be assigned a study-trained therapist who will provide hour-long weekly individual cognitive behavioral psychotherapy (CBT) based on current evidence-based practices for the treatment of anxiety and depressive symptoms for youth.
University of Cincinnati, Cincinnati
Stanford University, Stanford
National Institute of Mental Health (NIMH)
NIH
University of Cincinnati
OTHER