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Clinical Trials/NCT05118503
NCT05118503
Completed
N/A

Personalized Patient and Caregiver Education After Stroke

University of Pennsylvania1 site in 1 country120 target enrollmentOctober 20, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stroke, Acute
Sponsor
University of Pennsylvania
Enrollment
120
Locations
1
Primary Endpoint
Stroke Patient Education Retention (SPER) survey
Status
Completed
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 20, 2021
End Date
April 2, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christopher Favilla

Assistant Professor of Neurology

University of Pennsylvania

Eligibility Criteria

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

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

Outcomes

Primary Outcomes

Stroke Patient Education Retention (SPER) survey

Time Frame: 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

Time Frame: Day 90

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

Stroke etiology awareness

Time Frame: Day 90

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

EuroQOL-VAS

Time Frame: Day 90

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

Secondary Outcomes

  • SPER, 30 days(Day 30)
  • Stroke etiology awareness(Day 30)
  • Stroke risk factor awareness. 7 days(Day 7)
  • Stroke risk factor awareness, 30 days(Day 30)
  • Stroke risk factor awareness, 90 days(Day 90)
  • Stroke prevention med awareness, 7 days(Day 7)
  • Stroke prevention med awareness, 30 days(Day 30)
  • Stroke prevention med awareness, 90 days(Day 90)
  • Patient satisfaction, 7 days(Day 7)
  • Patient satisfaction, 30 days(Day 30)
  • SPER, 7 days(Day 7)

Study Sites (1)

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