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NCT07639606

Mobile Cognitive Behavioral Therapy in Early Stroke Recovery

Not Yet Recruiting
NAAges 18–79InterventionalTreatment
Weill Medical College of Cornell University
~10 participants
Updated 2026-06-30 on ClinicalTrials.gov
What's tested:Mobile Cognitive Behavioral Therapy App

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Feasibility and Acceptability of Maya as measured by the Mobile Application Rating Scale-User Version (uMARS)
Measured over Week 5 of treatment
+2 more outcomes measured

Conditions

Anxiety
Stroke
Depression - Major Depressive Disorder

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NCT07639606

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Weill Cornell Medicine

    New York, New Yorkstudy coordinator listed

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Study leadership

  • Abhishek Jaywant, PhD · PRINCIPAL_INVESTIGATOR · Weill Medical College of Cornell University

Who to contact

Abhishek Jaywant, PhD
[email protected]
212-746-4666
Email the study team

Opens a ready-to-send draft in your own email app — review before sending.

Want this trial checked against your situation?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Age 18-79
Positive screen on the Hospital Anxiety and Depression Scale (HADS), either the HADSD (depression, score \>= 8) and/or HADS-A (anxiety, score \>= 8).
Stroke that occurred within 1 month prior to study initiation.
Capacity to provide consent as determined by the UCSD Brief Assessment for Capacity to Consent (UBACC)
Montreal Cognitive Assessment (MoCA) score greater than or equal to 18, indicating no more than mild cognitive difficulties
Ability to use iPhone or iPad independently or through the assistance of a caregiver (participants will use their own iPhone if they have one, otherwise they will be loaned an iPad by the study team)
Able to adhere to all study requirements and willingness to participate in the full study duration

Exclusion

Aphasia or neglect that would interfere with use of the app, as determined through evaluation by speech-language pathology and occupational therapy conducted as part of standard clinical care
Non-fluency in English
History of a major neurologic disorder or of serious mental illness (bipolar or psychotic disorder, alcohol or substance use disorder as assessed through chart review)
Active suicidal ideation requiring a higher level of care
Severe depression and/or anxiety based on the initial evaluation and clinical judgment of the PI, which warrants a higher level of care and/or immediate referral to psychiatric services
Any other clinical or medical reason in the initial evaluation that suggests the study is not appropriate for the participant

What this trial measures

  • Feasibility and Acceptability of Maya as measured by the Mobile Application Rating Scale-User Version (uMARS)Week 5 of treatment

    Feasibility and acceptability will be measured by the scores collected on the uMARS by assessing the sub scores of Engagement, Functionality, Aesthetics, and Information of the app to measure the perceived quality of the app. The outcome is the mean of the individual items, ranging from 1 to 5, with 1 denoting minimal satisfaction/rating of app quality and 5 denoting maximum satisfaction and highest rating of app quality

  • Percent of Sessions completed over study time periodFrom Week 1 to Week 5 of treatment

    Feasibility will be assessed by the percentage of possible sessions completed

  • Percent of homework exercises completedFrom Week 1 to Week 5 of treatment

    Feasibility will be assessed by the percentage of assigned homework exercises that are completed