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Clinical Trial Summary

The primary objective will be to study changes in putamen connectivity and depression severity in depressed teens with meditation training. H1: Putamen node strength will increase in the training group compared to the active controls. H2: This increase in node strength will correlate with practice amount recorded by participants. H3: There will be a significant reduction in self-rated depression symptoms following the training as measured by the Reynolds Adolescent Depression Scale (RADS-2), compared to controls. H4: This reduction will correlate with the increase in putamen node strength. Design and Outcomes: The current research study design will utilize an individually randomized group treatment, open-label, active-controlled clinical trial to test the efficacy and safety of the investigator's innovative mindfulness meditation intervention (Training for Awareness Resilience and Action [TARA]) on the primary outcome (Putamen structural node strength) and secondary outcome (depression symptoms measured using Reynolds Adolescent Depression Scale [RADS-2]) in depressed adolescents between the ages of 14 to 18 years old.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05267340
Study type Interventional
Source University of California, San Francisco
Contact Olga Tymofiyeva, PhD
Phone 4152835406
Email Olga.Tymofiyeva@ucsf.edu
Status Recruiting
Phase N/A
Start date February 8, 2023
Completion date July 2025

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