Actively Recruiting
Personalized Mobile Cognitive Behavioral Therapy Application
Led by Weill Medical College of Cornell University · Updated on 2026-03-25
100
Participants Needed
1
Research Sites
151 weeks
Total Duration
On this page
Sponsors
W
Weill Medical College of Cornell University
Lead Sponsor
C
Children's Health Fund
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to compare the effectiveness of a standard mobile iPhone cognitive behavioral therapy program to a personalized mobile iPhone 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.
CONDITIONS
Official Title
Personalized Mobile Cognitive Behavioral Therapy Application
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 25 years.
- Primary diagnosis of anxiety, depressive, or bipolar disorder with a score of 4 or greater on the Anxiety Disorders Interview Schedule (ADIS).
- If diagnosed with bipolar disorder, must be currently euthymic or experiencing a depressive episode.
- Access to an Apple iPhone, iPad, or Android device.
You will not qualify if you...
- History of neurologic disorder affecting neural systems or ability to participate.
- Lifetime diagnosis of a psychotic disorder.
- Current hypomanic or manic episode.
- Currently receiving cognitive behavioral therapy.
- Change in psychiatric medication dose within the past 12 weeks.
- Started psychotherapy in the past 12 weeks.
- Intent or plan to attempt suicide.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Weill Cornell Medical College
New York, New York, United States, 10065
Actively Recruiting
Research Team
M
Maddy Schier
CONTACT
Z
Zareen Mir
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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