Purpose

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.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 25 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 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

Exclusion Criteria

  • History of neurologic disorder that may affect the neural systems of interest or participant's ability to participate - Lifetime diagnosis of a psychotic disorder. - Current hypomanic or manic episode. - Currently in cognitive behavior therapy. - Change in dose of a psychiatric medication in the past 12 weeks. - Initiation of psychotherapy in the past 12 weeks. - Intent or plan to attempt suicide.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Single (Investigator)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Personalized
Participants receive the personalized Maya app intervention for 6 weeks
  • Behavioral: Personalized MAYA Mobile App
    All new material in the personalized condition will be introduced within the first four weeks and will contain modules targeting participant's personal symptom profiles. The remaining two weeks in the personalized condition will consist of practicing previously learned skills.
  • Behavioral: General MAYA Mobile App
    New material will be introduced to participants over all the six weeks of the intervention and will include all application modules.
Active Comparator
General Non-Personalized
Participants receive the general MAYA app intervention for 6 weeks
  • Behavioral: General MAYA Mobile App
    New material will be introduced to participants over all the six weeks of the intervention and will include all application modules.

Recruiting Locations

More Details

Status
Recruiting
Sponsor
Weill Medical College of Cornell University

Study Contact

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

Detailed Description

Growing evidence suggests a need for anxiety and mood interventions that can be disseminated easily to adolescents and young adults. The goal of this study is to optimize a mobile application that teaches well-established, research-supported psychotherapeutic techniques to adolescents and young adults who are experiencing symptoms of anxiety, depression, and/or bipolar disorder. The study aims to compare the efficacy of a personalized mobile cognitive behavioral therapy program to a more general mobile cognitive behavioral therapy program. Study participants will randomly receive one of two versions of Maya, a mobile cognitive behavior therapy (CBT) app for adolescents and young adults: either a standard version that includes a variety of skills typically used in CBT, or a personalized version with skills matched to the participant's symptom profile. In contrast to the general condition, which may introduce new material over all six weeks of the intervention, all new material in the personalized condition will be introduced within the first four weeks. The remaining two weeks in the personalized condition will consist of practicing previously learned skills. Participants will use the Maya app for two days per week, at least 20 minutes per day for six weeks and will complete assessments at baseline, week 4, week 6 (end of intervention), and a follow-up assessment at week 12. Participants may also choose to complete an optional magnetic resonance imaging (MRI) and/or electroencephalographic (EEG) recording at the baseline and end of intervention (week 6).

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.