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NCT03076125 Clinical Trial

Stroke COunseling for Risk REduction

Stroke Clinical Trial

— SCORRE  

Official title:
Stroke Counseling for Risk Reduction in Young Adult African Americans

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03076125
Other study ID # K01NR015494
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2017
Est. completion date December 20, 2017

Study information
Verified date December 2018
Source Georgia State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to test the efficacy of the Stroke Counseling for Risk Reduction (SCORRE) intervention in increasing accuracy of perceived stroke risk and promoting lifestyle behavior change to reduce stroke risk in young adult African Americans.

Recruitment information / eligibility
Status Completed
Enrollment 116
Est. completion date December 20, 2017
Est. primary completion date December 20, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

- self-identify as African American/Black

- age 20-35 years

- able to complete two study visits lasing 1 1/2- 2 hours and a brief daily diary for 8 weeks

- has a cell phone or email address to receive weekly reminders and tips

- has at least one modifiable risk factor for stroke identified during study visit one screening

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• SCORRE
3 components based on the Health Belief Model
• Attention-Control Activity
sexual health education

Locations
Country Name City State
United States Georgia State University Atlanta Georgia

Sponsors (1)
Lead Sponsor Collaborator
Georgia State University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Accuracy of perceived stroke risk Comparison of perceived versus actual stroke risk immediately post-intervention
Primary Targeted health behaviors Improvements in targeted health behavior (physical activity, diet, or cigarette smoking) 8 weeks
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