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Study identifier: NCT05699525 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Personalized Mobile Cognitive Behavioral Therapy Application

Condition: Anxiety Disorders and Symptoms · Depression · Bipolar Disorder  ·  Sponsor: Weill Medical College of Cornell University

PhaseNA
Planned participants100
Who can joinAll sexes, 18 Years to 25 Years
Healthy volunteersNo

About this study

This study aims to compare the effectiveness of a standard mobile cognitive behavioral therapy program to a personalized mobile cognitive behavioral therapy program that introduces new skills over a shorter period of time. Participants will use the Maya app for two days per week, at least 20 minutes per day, for six weeks. Assessments will include a weekly check in with a member of the research team, questionnaires, and optional electroencephalographic (EEG) recordings at the beginning and end of the 6-week intervention. The investigators think that that the less burdensome personalized program will be just as effective at improving symptoms of anxiety and depression as the general program.

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

Talk to the study team

Maddy Schier  ·  (646) 289-5271  ·  mas4019@med.cornell.edu

Zareen Mir  ·  (646)-289-5271  ·  zam4005@med.cornell.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Weill Cornell Medical CollegeNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05699525