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Study identifier: NCT07098169 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Randomized Clinical Trial of iTEST: A Blended Intervention Targeting Introspective Accuracy

Condition: Schizophrenia Disorders · Schizoaffective Disorder · Psychotic Disorder  ·  Sponsor: University of California, San Diego

PhaseNA
Planned participants201
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the effectiveness of a psychosocial intervention called iTEST for people with psychotic disorders that targets introspective accuracy, or the ability to accurately gauge ones abilities. iTEST combines daily cognitive training on a mobile device with coaching that addresses recovery goals. In this trial, we will randomize people to one of two interventions conditions, iTEST or a control condition that receives coaching and cognitive training that does not emphasize introspective accuracy. Both interventions will take place over 12 weeks and participants will be asked to complete assessments at baseline, 6 weeks, 12 weeks, and 24 weeks. The primary outcome of the study is community functioning. Participants will be from three metropolitan areas: San Diego, Dallas, or Miami.

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

Talk to the study team

Colin A Depp, Ph.D.  ·  858-822-4251  ·  cdepp@ucsd.edu

Nikki Abaya, MA  ·  (858) 869 0031  ·  niabaya@health.ucsd.edu

Always discuss trial participation with your own doctor first.

Locations (3)

UC San DiegoSan Diego, California, United StatesRecruiting
University of MiamiMiami, Florida, United StatesRecruiting
University of Texas at DallasDallas, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07098169