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N/A N=101 Other

A Community Partnership to Treat Stroke

Stroke

Enrolled (actual)
101
Serious AEs
0.0%
Results posted
Sep 2017
Primary outcome: Primary: Completion — 64 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Stroke Preparedness Intervention (Behavioral)
Age
Pediatric, Adult, Older Adult · 10+ yrs
Sex
All
Sponsor
University of Michigan
Primary completion
Aug 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Completion
64
SECONDARY
Mean Change in Behavioral Intent to Call 911
4.4; 5.2 <0.01 sig
SECONDARY
Mean Change in Stroke Recognition
5.9; 6.0 0.34
SECONDARY
Perception of Social Norms Clustered Within Churches Across Multiple Time Points
-0.5; 0.2; -0.9; 0.1
SECONDARY
Perception of Self-efficacy Clustered Within Churches Across Multiple Time Points
1.2; .8; .8; .3
SECONDARY
Perception of Stroke Attitude Clustered Within Churches Across Multiple Time Points
.05; 0.3; -0.07; -0.5

Summary

Getting to the hospital quickly is the key to treating stroke. African Americans suffer more strokes with worse outcomes and receive stroke treatments less often than European Americans. This project will work to reduce these health disparities by creating and testing the feasibility of a peer-led faith-based behavioral intervention in an African American community with a goal to increase calls to 911 so stroke patients can be treated quickly.

Eligibility Criteria

Inclusion Criteria

To meet participant eligibility criteria, individuals must be 18 years of age or older (adult intervention) or between 10-17 years of age (youth intervention), a resident of the Flint or greater Flint community, and English speaking.

Exclusion Criteria

We will attempt to exclude those who cannot read English because they will not be able to benefit from the intervention materials. These criteria will be confirmed during assessment procedures prior to enrollment.

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01499173). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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