RECRUITING

Mobile Cognitive Behavioral Therapy for Stroke

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Mobile Cognitive Behavioral Therapy for Stroke

Quick Facts

Study Start:2025-02-25
Study Completion:2028-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06689878

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:40 Years to 79 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 40-79
  2. * Presence of clinically-significant anxiety and/or depression (as determined by an eligibility evaluation)
  3. * Stroke that occurred 1 month or more prior to study initiation
  4. * Capacity to provide consent
  5. * No greater than mild cognitive difficulties based on an eligibility evaluation conducted as part of the study
  6. * If taking medication for depression and/or anxiety, must be on a stable dose for a minimum of 8 weeks prior to study initiation
  7. * Ability to use iPhone or iPad independently
  8. * Home internet access
  9. * Willingness to participate in the full study duration.
  1. * Aphasia of moderate or greater severity (as determined during an eligibility evaluation)
  2. * Non-fluency in English
  3. * History of a bipolar or psychotic disorder
  4. * Current alcohol or substance use disorder
  5. * Active suicidal ideation
  6. * Current engagement in psychotherapy is not grounds for exclusion unless the individual's psychotherapy is primarily focused on CBT
  7. * 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
  8. * Any other clinical or medical reason in the study doctor's initial screening evaluation that suggests the study is not appropriate for the participant

Contacts and Locations

Study Contact

Abhishek Jaywant, PhD
CONTACT
212-746-4666
abj2006@med.cornell.edu

Principal Investigator

Abhishek Jaywant, PhD
PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University

Study Locations (Sites)

Weill Cornell Medicine
New York, New York, 10065
United States

Collaborators and Investigators

Sponsor: Weill Medical College of Cornell University

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

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-02-25
Study Completion Date2028-03

Study Record Updates

Study Start Date2025-02-25
Study Completion Date2028-03

Terms related to this study

Keywords Provided by Researchers

  • stroke recovery
  • stroke rehabilitation
  • cognitive behavioral therapy
  • CBT

Additional Relevant MeSH Terms

  • Anxiety
  • Stroke
  • Depression