Personalized Patient and Caregiver Education After Stroke
- Conditions
- StrokeStroke, IschemicStroke, Acute
- Interventions
- Behavioral: Customized educationBehavioral: Standard of care discharge education
- Registration Number
- NCT05118503
- Lead Sponsor
- University of Pennsylvania
- Brief Summary
This is a randomized pilot trial to evaluate the impact of a customizable stroke education app (vs standard of care discharge education) on patient satisfaction and education retention. The impact of the intervention will be assessed 7, 30, and 90 days post-discharge.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 120
- Admitted for ischemic stroke
- At least 18 years old
- Patient or caregiver has access to a smart phone, tablet or computer
- Being discharged to either home or acute rehab
- Patient or caregivers unable or unwilling to access the customized app with a smartphone, tablet, or computer
- Being discharged to a skilled nursing facility
- moderate-to-severe aphasia at the time of enrollment (as per NIHSS scoring) if patient is being enrolled without a caregiver
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Customized education app Customized education A customized URL-based platform will present brief education videos addressing a patients stroke etiology, risk factors, stroke prevention medications, and post-stroke lifestyle issues. This URL will be made available to the patient and caregiver. Standard of care discharge education Standard of care discharge education Standard discharge education is performed by the bedside nurse at the time of hospital discharge.
- Primary Outcome Measures
Name Time Method Stroke Patient Education Retention (SPER) survey Day 90 Validated measure of stroke patient education as it pertains to their stroke etiology and risk factors with scores of 0-10
Patient satisfaction survey Day 90 Likert-style survey assessing patient satisfaction and perception of the stroke education they received.
Stroke etiology awareness Day 90 accurate knowledge of stroke etiology (0=incorrect; 1=correct)
EuroQOL-VAS Day 90 validated quality of life metric, with scores of 0-100
- Secondary Outcome Measures
Name Time Method SPER, 30 days Day 30 Stroke Patient Education Retention (SPER) survey
Stroke etiology awareness Day 30 accurate knowledge of stroke etiology (0=incorrect; 1=correct)
Stroke risk factor awareness. 7 days Day 7 accurate knowledge of stroke risk factors (0=incorrect; 1=correct)
Stroke risk factor awareness, 30 days Day 30 accurate knowledge of stroke risk factors (0=incorrect; 1=correct)
Stroke risk factor awareness, 90 days Day 90 accurate knowledge of stroke risk factors (0=incorrect; 1=correct)
Stroke prevention med awareness, 7 days Day 7 accurate knowledge of stroke prevention medications (0=incorrect; 1=correct)
Stroke prevention med awareness, 30 days Day 30 accurate knowledge of stroke prevention medications (0=incorrect; 1=correct)
Stroke prevention med awareness, 90 days Day 90 accurate knowledge of stroke prevention medications (0=incorrect; 1=correct)
Patient satisfaction, 7 days Day 7 Likert-style survey assessing patient satisfaction and perception of the stroke education
Patient satisfaction, 30 days Day 30 Likert-style survey assessing patient satisfaction and perception of the stroke education
SPER, 7 days Day 7 Stroke Patient Education Retention (SPER) survey
Trial Locations
- Locations (1)
Hospital of the University of Pennsylvania
🇺🇸Philadelphia, Pennsylvania, United States