NCT05699525Recruiting
Personalized Mobile Cognitive Behavioral Therapy Application
Efficacy of Personalized Mobile Cognitive Behavioral Therapy Targeting Anxiety and Depression
Source: ClinicalTrials.gov · Last updated 22 May 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- First submitted
- 17 Jan 2023
- Start date
- 2 Aug 2024
- Primary completion date
- Jul 2027
- Lead sponsor
- Weill Medical College of Cornell University
- Diseases
- Bipolar disorder
- NCT number
- NCT05699525
What you commit to
- Study type: Interventional
- Planned participants: 100
- From 2 Aug 2024 to the primary completion date, Jul 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Currently in cognitive behavior therapy.
Other illness
- History of neurologic disorder that may affect the neural systems of interest or participant's ability to participate
- Lifetime diagnosis of a psychotic disorder.
- Change in dose of a psychiatric medication in the past 12 weeks.
Other
- Current hypomanic or manic episode.
- Initiation of psychotherapy in the past 12 weeks.
- Intent or plan to attempt suicide.
Who the study is looking for
- 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, iPad, or Android device.
Age in the registry: 18 years to 25 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Weill Cornell Medical College Coordinator of this site? Confirm its status | New York | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.