Stroke Ready: A Stroke Preparedness Brief Intervention
Overview
This is a randomized controlled behavioral intervention trial to assess the efficacy of a brief intervention to increase stroke preparedness.
Study Type
- Study Type: Interventional
- Study Design
- Allocation: Randomized
- Intervention Model: Crossover Assignment
- Primary Purpose: Health Services Research
- Masking: None (Open Label)
- Study Primary Completion Date: April 23, 2019
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
Interventions
- Behavioral: Stroke preparedness intervention
- Face-to-face interaction with research staff lasting between 5-10 minutes
- Behavioral: Healthy lifestyle stroke risk reduction intervention
- Face-to-face interaction with research staff lasting between 5-10 minutes
Arms, Groups and Cohorts
- Experimental: Stroke Preparedness Intervention
- The stroke preparedness educational intervention was designed with input from the community where it is being tested. It will be delivered in-person by a research team member. The intervention focuses on recognizing stroke symptoms and the importance of calling 911.
- Active Comparator: Healthy lifestyle intervention
- The Healthy lifestyle stroke risk reduction educational intervention is based on patient materials from the American Heart Association. It will be delivered in-person by a research team member. The intervention focuses on stroke risk reduction.
Clinical Trial Outcome Measures
Primary Measures
- Change in Behavioral Intent to Call 911
- Time Frame: Immediately (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.
Participating in This Clinical Trial
Inclusion Criteria
- over 18 years of age Exclusion Criteria:
- none
Gender Eligibility: All
Minimum Age: 18 Years
Maximum Age: N/A
Are Healthy Volunteers Accepted: Accepts Healthy Volunteers
Investigator Details
- Lead Sponsor
- University of Michigan
- Provider of Information About this Clinical Study
- Principal Investigator: Lesli E. Skolarus, MD, Associate Professor of Neurology – University of Michigan
- Overall Official(s)
- Lesli Skolarus, MD, MS, Principal Investigator, University of Michigan
Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.