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Personalized Patient and Caregiver Education After Stroke

Not Applicable
Completed
Conditions
Stroke
Stroke, Ischemic
Stroke, Acute
Interventions
Behavioral: Customized education
Behavioral: 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
Inclusion Criteria
  • 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
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Exclusion Criteria
  • 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
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Customized education appCustomized educationA 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 educationStandard of care discharge educationStandard discharge education is performed by the bedside nurse at the time of hospital discharge.
Primary Outcome Measures
NameTimeMethod
Stroke Patient Education Retention (SPER) surveyDay 90

Validated measure of stroke patient education as it pertains to their stroke etiology and risk factors with scores of 0-10

Patient satisfaction surveyDay 90

Likert-style survey assessing patient satisfaction and perception of the stroke education they received.

Stroke etiology awarenessDay 90

accurate knowledge of stroke etiology (0=incorrect; 1=correct)

EuroQOL-VASDay 90

validated quality of life metric, with scores of 0-100

Secondary Outcome Measures
NameTimeMethod
SPER, 30 daysDay 30

Stroke Patient Education Retention (SPER) survey

Stroke etiology awarenessDay 30

accurate knowledge of stroke etiology (0=incorrect; 1=correct)

Stroke risk factor awareness. 7 daysDay 7

accurate knowledge of stroke risk factors (0=incorrect; 1=correct)

Stroke risk factor awareness, 30 daysDay 30

accurate knowledge of stroke risk factors (0=incorrect; 1=correct)

Stroke risk factor awareness, 90 daysDay 90

accurate knowledge of stroke risk factors (0=incorrect; 1=correct)

Stroke prevention med awareness, 7 daysDay 7

accurate knowledge of stroke prevention medications (0=incorrect; 1=correct)

Stroke prevention med awareness, 30 daysDay 30

accurate knowledge of stroke prevention medications (0=incorrect; 1=correct)

Stroke prevention med awareness, 90 daysDay 90

accurate knowledge of stroke prevention medications (0=incorrect; 1=correct)

Patient satisfaction, 7 daysDay 7

Likert-style survey assessing patient satisfaction and perception of the stroke education

Patient satisfaction, 30 daysDay 30

Likert-style survey assessing patient satisfaction and perception of the stroke education

SPER, 7 daysDay 7

Stroke Patient Education Retention (SPER) survey

Trial Locations

Locations (1)

Hospital of the University of Pennsylvania

🇺🇸

Philadelphia, Pennsylvania, United States

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