Efficacy of Personalized Mobile Cognitive Behavioral Therapy Targeting Anxiety and Depression

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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 magnetic resonance imaging (MRI) and 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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 25
Healthy Volunteers: f
View:

• Age between 18 and 25 years.

• Primary diagnosis of an anxiety, depressive, or bipolar disorder as determined by a score of 4 or greater on the Clinical Severity Rating of the Anxiety Disorders Interview Schedule (ADIS).

• If an individual is diagnosed with bipolar disorder, they must be currently euthymic or experiencing a depressive episode.

• Access to an Apple iPhone

Locations
United States
New York
Weill Cornell Medical College
RECRUITING
New York
Contact Information
Primary
Maddy Schier
mas4019@med.cornell.edu
(646) 289-5271
Backup
Zareen Mir
zam4005@med.cornell.edu
(646)-289-5271
Time Frame
Start Date: 2024-08-02
Estimated Completion Date: 2027-07
Participants
Target number of participants: 100
Treatments
Experimental: Personalized
Participants receive the personalized Maya app intervention for 6 weeks
Active_comparator: General Non-Personalized
Participants receive the general MAYA app intervention for 6 weeks
Related Therapeutic Areas
Sponsors
Collaborators: Children's Health Fund
Leads: Weill Medical College of Cornell University

This content was sourced from clinicaltrials.gov