Personalized Video-based Education for Chronic Stroke Survivors: A Randomized Clinical Trial
Overview
- Phase
- Not Applicable
- Intervention
- Standard Education
- Conditions
- Stroke
- Sponsor
- University of Pennsylvania
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- Patient satisfaction with stroke education (90 days)
- Status
- Active, not recruiting
- Last Updated
- 2 months ago
Overview
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.
Investigators
Christopher Favilla
Assistant Professor of Neurology
University of Pennsylvania
Eligibility Criteria
Inclusion Criteria
- •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)
Exclusion Criteria
- •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)
Arms & Interventions
Standard Education
Standard stroke patient education as per the medical providers
MyStroke
Access to a personalized video-based stroke educational platform
Intervention: MyStroke
Outcomes
Primary Outcomes
Patient satisfaction with stroke education (90 days)
Time Frame: 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)
Stroke risk factor recognition (90 days)
Time Frame: 90 days
The proportion of patients who correctly identify at least one of their vascular risk factors
Stroke etiology recognition (90 days)
Time Frame: 90 days
The proportion of patients who correctly identify their stroke etiology
Secondary Outcomes
- Stroke patient education retention (SPER) survey (90 days)(90 days)
- Patient satisfaction with stroke education (7 days)(7 days)
- Stroke etiology recognition (7 days)(7 days)
- Stroke patient education retention (SPER) survey (7 days)(7 days)
- Stroke prevention medication recognition (90 days)(90 days)
- Stroke prevention medication recognition (7 days)(7 days)
- EuroQOL - visual analog scale (7 days)(7 days)
- Medication adherence (7 days)(7 days)
- Stroke risk factor recognition (7 days)(7 days)
- EuroQOL - visual analog scale (90 days)(90 days)
- modified Rankin Scale(90 days)
- Medication adherence (90 days)(90 days)