Mobile Cognitive Behavioral Therapy for Stroke

Part of paid clinical trials in New York, New York.

Sponsor
Weill Medical College of Cornell University
Study ID
NCT06689878
Status
Recruiting
Apply to this trial

Conditions

Eligibility Criteria

Sex
ALL
Age
40 Years - 79 Years
Healthy Volunteers
Not accepted

Interventions

  • Mobile Cognitive Behavioral App — BEHAVIORAL
    A mobile cognitive behavioral therapy (CBT) app called "Maya" that includes modules with educational content and teaching and practice of strategies that address depression and anxiety after stroke.

Study Details

This study aims to assess the feasibility and acceptability of "MAYA", a mobile cognitive behavioral therapy app for anxiety and mood disorders, in adults who have had a stroke.

Key Dates

Start date
Feb 25, 2025
Status verified
Mar 2026
Primary completion
Mar 31, 2028
Completion
Mar 31, 2028

Study Design

Enrollment
10 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Intervention Arm Using the Mobile Cognitive Behavioral Therapy App
    All participants will receive the same intervention arm, a mobile cognitive behavioral therapy (CBT) app that includes modules with educational content and teaching and practice of strategies that address the following: education about anxiety and depression and their association with stroke recovery; awareness and monitoring of emotions; behavioral activation, i.e., increasing engagement in valued and meaningful activities; increasing awareness of thinking errors and reframing negative thoughts; mindfulness; relaxation skills; increasing tolerance of anxiety in anxiety-provoking situations; and problem-solving. The application includes an interactive dashboard to provide the user with statistics for tracking progress toward their goals. Participants will be asked to use the application for 30 minutes per day, 2 days per week, for 8 weeks.

Primary Outcome Measure

Feasibility and Acceptability of MAYA as measured by the Mobile Application Rating Scale-User Version (uMARS) [ Time Frame: Week 4 of treatment ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Weill Cornell MedicineNew YorkNew York10065
Abhishek Jaywant, PhD
[email protected]
212-746-4666
Abhishek Jaywant, PhD (PRINCIPAL_INVESTIGATOR)

Find similar trials in New York, NY

By condition
DepressionStroke
By specialty
PsychiatryMental healthBehavioral healthNeurologyBrain disorders
By research site
Weill Cornell Medicine· New York, NY

Related Studies