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Study identifier: NCT06273137 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Positive Affect Treatment for Adolescents With Early Life Adversity

Condition: Depression  ·  Sponsor: University of California, Irvine

PhaseNA
Planned participants300
Who can joinAll sexes, 12 Years to 16 Years
Healthy volunteersYes

About this study

Youth exposed to early life adversity (ELA) are known to be at greater risk for depression and suicidality and account for almost half of the youth suffering from psychiatric diseases today. Youth exposed to ELA consistently report symptoms of anhedonia as well as dysregulated positive affect. The present project will test the efficacy of PAT in a sample of ELA-exposed adolescents in order to determine whether PAT increases positive affect, and subsequently symptoms of depression. For the initial pilot phase of the investigation, the investigators will recruit up to 30 adolescents exposed to two or more childhood adversities (ACEs) who do not currently have major depressive disorder, and randomize them (1:1) to either participate in PAT or a waitlist control condition. For the second phase of the investigation, the investigators will recruit up to 300 adolescents exposed to two or more childhood adversities (ACEs) who do not currently have major depressive disorder, and randomize them (1:1) to either participate in PAT or supportive psychotherapy. For both phases, at study enrollment, then 4-, 8, and 12-months thereafter the investigators will measure positive affect and depressive symptoms (including anhedonia and reward sensitivity). The results of this study will be used to inform whether PAT has the potential to prevent major depressive episodes among adversity-exposed youth.

This description comes directly from the study's public registry record.

Talk to the study team

Kate R Kuhlman, Ph.D.  ·  9498245574  ·  krkuhl@uci.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of California IrvineIrvine, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06273137