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

Eligibility Criteria

Sex
ALL
Age
18 Years - 25 Years
Healthy Volunteers
Not accepted

Interventions

  • Personalized MAYA Mobile App — BEHAVIORAL
    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.
  • General MAYA Mobile App — BEHAVIORAL
    New 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: 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

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

Locations (1)

FacilityCityStateZIPSite coordinators
Weill Cornell Medical CollegeNew YorkNew York10065
Jennifer Bress, Ph.D
914.997.8683
Maddy Schier
(646) 289-5271
Jennifer Bress, Ph.D (PRINCIPAL_INVESTIGATOR)

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