ClinicalTrials.Veeva

Menu

Stroke COunseling for Risk REduction (SCORRE)

Georgia State University logo

Georgia State University

Status

Completed

Conditions

Stroke

Treatments

Behavioral: SCORRE
Behavioral: Attention-Control Activity

Study type

Interventional

Funder types

Other

Identifiers

NCT03076125
K01NR015494

Details and patient eligibility

About

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.

Enrollment

116 patients

Sex

All

Ages

20 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

116 participants in 2 patient groups

SCORRE group
Experimental group
Description:
Stroke risk factor brochure, stroke champions video, counseling on accuracy of perceived stroke risk and strategies to reduce stroke risk, weekly motivational health behavior tips (for physical activity, diet, or smoking cessation) text messages for 8 weeks.
Treatment:
Behavioral: SCORRE
Attention Control Group
Sham Comparator group
Description:
Sexual health education brochure and Safe in the City video, weekly sexual health tips text messages for 8 weeks.
Treatment:
Behavioral: Attention-Control Activity

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems