🏛️ Verified NIH Record • Updated 2026-07-31

Mobile Cognitive Behavioral Therapy for Stroke (NCT06689878)

🟢 Recruiting Observational / Diagnostic ⚙️ Medical Device Protocol Sponsor: Weill Medical College of Cornell University

🩺 Plain-English Summary (8th-Grade Level)

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.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (9 items) and avoid the listed exclusions (9 items).

Location: Weill Cornell Medicine — New York, New York

Age range: 40 Years to 79 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Usually NOT eligible if any of the following apply:

  • 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

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (1 Sites)

  • Weill Cornell Medicine — New York, New York

📞 Contact the Study Coordinator

Phone: (212) 746-4666

Email: abj2006@med.cornell.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Anxiety clinical trials

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗