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Stroke Ready: A Stroke Preparedness Brief Intervention

Not Applicable
Completed
Conditions
Stroke
Registration Number
NCT03831451
Lead Sponsor
University of Michigan
Brief Summary

This is a randomized controlled behavioral intervention trial to assess the efficacy of a brief intervention to increase stroke preparedness.

Detailed Description

This is a randomized controlled behavioral intervention trial to assess the efficacy of a brief intervention to increase stroke preparedness. Subjects will be randomized to a brief face-to-face stroke preparedness intervention compared to a healthy lifestyle stroke risk reduction intervention. The primary outcome is behavioral intent to call 911 using a self-administered survey

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
129
Inclusion Criteria
  • over 18 years of age
Exclusion Criteria
  • none

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
Change in Behavioral Intent to Call 911Immediately (up to 10 minutes) before the brief intervention and then immediately (up to 10 minutes) after completing the brief intervention

Change in Behavioral intent to call 911 using a self-administered survey. The survey is the Stroke Action test which was modified based on community input. Scores range from 0-12 for stroke. A higher score means greater stroke behavioral intent to call 911 for a stroke while a low score means lower behavioral intent to call 911 for a stroke.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

Hamilton Community Health Network

🇺🇸

Flint, Michigan, United States

Hasselbring Senior Center

🇺🇸

Flint, Michigan, United States

Hamilton Community Health Network
🇺🇸Flint, Michigan, United States

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