Personalized Mobile Cognitive Behavioral Therapy Application
Part of paid clinical trials in New York, New York.
- Sponsor
- Weill Medical College of Cornell University
- Study ID
- NCT05699525
- Status
- Recruiting
Conditions
- Anxiety Disorders and Symptoms
- Bipolar Disorder
- Depression
- Symptoms
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 25 Years
- Healthy Volunteers
- Not accepted
Interventions
- Personalized MAYA Mobile App — BEHAVIORALAll 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.
- General MAYA Mobile App — BEHAVIORALNew material will be introduced to participants over all the six weeks of the intervention and will include all application modules.
Study Details
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.
Key Dates
- Start date
- Aug 2, 2024
- Status verified
- May 2026
- Primary completion
- Jul 31, 2027
- Completion
- Jul 31, 2027
Study Design
- Enrollment
- 100 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: PersonalizedParticipants receive the personalized Maya app intervention for 6 weeks
- Active Comparator: General Non-PersonalizedParticipants receive the general MAYA app intervention for 6 weeks
Primary Outcome Measure
Change in anxiety symptoms from pre-intervention to post-intervention as measured by the HAM-A. [ Time Frame: Baseline to endpoint [Week 6] ]
Central Contacts
- Maddy Schier(646) 289-5271
- Zareen Mir(646)-289-5271
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Weill Cornell Medical College | New York | New York | 10065 | Jennifer Bress, Ph.D (PRINCIPAL_INVESTIGATOR) |
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