MyStroke in Chronic Stroke
Personalized Video-based Education for Chronic Stroke Survivors: A Randomized Clinical Trial
1 other identifier
interventional
100
1 country
1
Brief Summary
This is a single-center randomized control trial assessing the impact of a personalized video-based educational platform on patients satisfaction and stroke knowledge in the context of chronic stroke.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable stroke
Started Oct 2023
Typical duration for not_applicable stroke
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 22, 2023
CompletedFirst Posted
Study publicly available on registry
September 28, 2023
CompletedStudy Start
First participant enrolled
October 17, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 15, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2026
CompletedFebruary 13, 2026
February 1, 2026
12 months
August 22, 2023
February 10, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Patient satisfaction with stroke education (90 days)
5-point Likert-scale (Q: I am satisfied with the quality of my stroke education; Answers range from strongly disagree to strongly agree)
90 days
Stroke etiology recognition (90 days)
The proportion of patients who correctly identify their stroke etiology
90 days
Stroke risk factor recognition (90 days)
The proportion of patients who correctly identify at least one of their vascular risk factors
90 days
Secondary Outcomes (12)
Stroke prevention medication recognition (7 days)
7 days
Stroke prevention medication recognition (90 days)
90 days
Patient satisfaction with stroke education (7 days)
7 days
Stroke etiology recognition (7 days)
7 days
Stroke risk factor recognition (7 days)
7 days
- +7 more secondary outcomes
Study Arms (2)
Standard Education
NO INTERVENTIONStandard stroke patient education as per the medical providers
MyStroke
EXPERIMENTALAccess to a personalized video-based stroke educational platform
Interventions
Eligibility Criteria
You may qualify if:
- History of ischemic stroke between 1 and 10 years prior to enrollment
- Receiving outpatient stroke care at the Hospital of the University of Pennsylvania
- At least 18 years old
- Access to a smart phone, tablet, or computer
- Willingness to complete 2 follow-up surveys (7 days and 90 day post-enrollment)
You may not qualify if:
- Unwilling or unable to access the customized app with a smartphone, tablet, or computer
- Complete dependence on caregiver for all activities of daily living
- Stroke occurred less than 1 year or greater than 10 years prior to screening/enrollment
- Patient has severe aphasia (score of greater than or equal to 2 on National Institutes of Health Stroke Scale item 9)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Hospital of the University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor of Neurology
Study Record Dates
First Submitted
August 22, 2023
First Posted
September 28, 2023
Study Start
October 17, 2023
Primary Completion
October 15, 2024
Study Completion
April 1, 2026
Last Updated
February 13, 2026
Record last verified: 2026-02