Mobile app for cognitive behavioral therapy in stroke recovery
Official title: Mobile Cognitive Behavioral Therapy for Stroke
Run by Weill Medical College of Cornell University · NCT06689878 · Data updated 2026-11-12
This study tests a mobile app called 'MAYA' to see if it can help adults recovering from a stroke manage anxiety and depression through cognitive behavioral therapy.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 40 Years to 79 Years |
| Sex | All |
| Enrollment | 10 (estimated) |
| Sponsor | Weill Medical College of Cornell University Academic / other |
| Locations | 1 site (New York, New York) |
| Status | Recruiting |
| Started | February 25, 2025 |
| Main results expected | March 2028 |
| Study ends | March 2028 |
| Registry record updated | August 4, 2026 |
| Trial ID | NCT06689878 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 40-79 who have experienced a stroke at least one month prior and have clinically significant anxiety or depression.
✕Probably not a fit
Patients with moderate to severe aphasia, active suicidal ideation, or those currently engaged in psychotherapy focused on CBT may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the feasibility and acceptability of 'MAYA', a mobile cognitive behavioral therapy app designed for adults who have experienced a stroke. Participants will use the app for at least two days a week over an 8-week period, with weekly check-ins to monitor adherence and mood symptoms. The study will assess the number of sessions completed and gather qualitative feedback, as well as preliminary efficacy on anxiety and depression symptoms using standardized measures.
Why it matters
Potential benefit: If successful, this intervention could improve mental health outcomes for stroke survivors dealing with anxiety and depression.
How similar studies have gone: Other studies have shown promise in using mobile CBT applications for mental health, suggesting potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 40-79 * Presence of clinically-significant anxiety and/or depression (as determined by an eligibility evaluation) * Stroke that occurred 1 month or more prior to study initiation * Capacity to provide consent * No greater than mild cognitive difficulties based on an eligibility evaluation conducted as part of the study * If taking medication for depression and/or anxiety, must be on a stable dose for a minimum of 8 weeks prior to study initiation * Ability to use iPhone or iPad independently * Home internet access * Willingness to participate in the full study duration. Exclusion Criteria: * Aphasia of moderate or greater severity (as determined during an eligibility evaluation) * Non-fluency in English * History of a bipolar or psychotic disorder * Current alcohol or substance use disorder * Active suicidal ideation * Current engagement in psychotherapy is not grounds for exclusion unless the individual's psychotherapy is primarily focused on CBT * Severe depression and/or anxiety based on the initial evaluation and clinical judgment of the study doctor, which warrants a higher level of care and/or immediate referral to psychiatric services * Any other clinical or medical reason in the study doctor's initial screening evaluation that suggests the study is not appropriate for the participant
Where it's running
-
Weill Cornell Medicine
New York, New York, United States Recruiting
Study contacts
- Principal investigator: Abhishek Jaywant, PhD — Weill Medical College of Cornell University
- Study coordinator: Abhishek Jaywant, PhD
- Email: abj2006@med.cornell.edu
- Phone: 212-746-4666
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Pharmacy-led intervention to improve medication adherence after hospital discharge
This study tests a pharmacy-led program to help low-income patients with multiple chronic conditions take their medications correctly after leaving the hospital.
-
Mindful Smartphone Use: A Mindfulness-Based Program for Teens with Sleep and Mood Challenges
This study tests Mindwire, a mindfulness-based program, to see if it helps teens with problematic phone use who also have depression or anxiety.
-
Tele-based wellbeing centres for women's mental health in Bangladesh
A randomized trial tests whether tele-counselling for depression and anxiety in Bangladeshi women is as effective as in-person counselling.
-
HBOT to see if it helps cognition and well‑being in first responders with prior brain injury
This study tests whether 40 hyperbaric oxygen therapy sessions can improve thinking skills and post-concussion symptoms in current or former first responders with a history of brain injury.
-
Focused ultrasound for mood and anxiety disorders
This study tests whether repeated low-intensity focused ultrasound using the ATTN201 device can help people with subsyndromal to moderate depression, anxiety, or OCD.
-
An Ultra-Brief ICBT Intervention with Personal Feedback for Depression and Anxiety
This trial tests whether adding personalized feedback about a person’s recent healthy actions to the Things You Do ultra-brief online CBT program helps adults with depression and anxiety do more healthy activities and feel better.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.