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Mobile Cognitive Behavioral Therapy App for Anxiety and Depression

N/A
Recruiting
Led By Jennifer Bress, Ph.D.
Research Sponsored by Weill Medical College of Cornell University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to end of active learning phase [week 4 for personalized intervention and week 6 for the general intervention]
Awards & highlights

Summary

This trial aims to compare two mobile CBT programs for anxiety/depression. Participants use Maya app 2 days/wk, 20 min/day. Assessments include questionnaires & optional MRI/EEG. Investigators think personalized program can be just as effective.

Who is the study for?
This trial is for young adults aged 18-25 with anxiety, depression, or bipolar disorder (currently in a depressive episode), who haven't started new psychotherapy or changed medication doses in the last 12 weeks. It's not for those with psychotic disorders, current manic episodes, or immediate suicide risk.
What is being tested?
The study compares two mobile apps delivering cognitive behavioral therapy: a standard version and a personalized one that introduces skills faster. Participants will use an app twice weekly for six weeks and undergo assessments including questionnaires and optional brain scans.
What are the potential side effects?
Since this trial involves non-invasive therapy through an app, there are no direct physical side effects like you'd expect from medication. However, discussing mental health can sometimes cause emotional discomfort.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to end of active learning phase [week 4 for personalized intervention and week 6 for the general intervention]
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline to end of active learning phase [week 4 for personalized intervention and week 6 for the general intervention] for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in anxiety symptoms from pre-intervention to post-intervention as measured by the HAM-A.
Change in anxiety symptoms from pre-intervention to post-intervention as measured by the anxiety subscale of the DASS.
Change in depressive symptoms from pre-intervention to post-intervention as measured by HAM-D.
+1 more
Secondary study objectives
Bipolar symptoms from pre-intervention to post-intervention as measured by ISS.
Change in Negative affect from pre-intervention to post-intervention as measured by PANAS
Change in anhedonia from pre-intervention to post-intervention as measured by TEPS.
+7 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: PersonalizedExperimental Treatment1 Intervention
Participants receive the personalized Maya app intervention for 6 weeks
Group II: General Non-PersonalizedActive Control1 Intervention
Participants receive the general MAYA app intervention for 6 weeks

Find a Location

Who is running the clinical trial?

Weill Medical College of Cornell UniversityLead Sponsor
1,077 Previous Clinical Trials
1,320,567 Total Patients Enrolled
4 Trials studying Bipolar Disorder
543 Patients Enrolled for Bipolar Disorder
Children's Health FundUNKNOWN
Jennifer Bress, Ph.D.Principal InvestigatorWeill Medical College of Cornell University
1 Previous Clinical Trials
60 Total Patients Enrolled

Media Library

General MAYA Mobile App Clinical Trial Eligibility Overview. Trial Name: NCT05699525 — N/A
Bipolar Disorder Research Study Groups: Personalized, General Non-Personalized
Bipolar Disorder Clinical Trial 2023: General MAYA Mobile App Highlights & Side Effects. Trial Name: NCT05699525 — N/A
General MAYA Mobile App 2023 Treatment Timeline for Medical Study. Trial Name: NCT05699525 — N/A
~67 spots leftby Jan 2025
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