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Trial of a Secondary Stroke Prevention Program

Development of a Stroke Prevention Program for an Underserved Minority Community

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01071408
Enrollment
54
Registered
2010-02-19
Start date
2010-03-31
Completion date
2012-05-31
Last updated
2012-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic Stroke, Transient Ischemic Attack

Keywords

chronic care model, stroke prevention, health services research

Brief summary

The purpose of this study is to determine whether an outpatient program can reduce the risk of recurrent stroke.

Detailed description

Stroke is a major cause of death and disability. A history of stroke is the strongest predictor of a future stroke. Control of risk factors lowers the risk of future stroke, yet most persons with stroke do not have their risk factors controlled. In this randomized-controlled trial, we will test whether an outpatient stroke prevention program consisting of group clinics, patient self-management, and telephone care coordination can lower the risk of recurrent stroke by improving patient knowledge, medication adherence, and lifestyle habits. If successful, this program may be adapted to other settings.

Interventions

OTHERStroke prevention care program

Stroke prevention care program consists of group clinics, telephone coordination of care, and tracking of care through registries in the first 7 months after stroke or TIA presentation. A nurse practitioner will follow algorithms to adjust medications and to motivate patients to improve lifestyle habits.

Sponsors

National Institute of Neurological Disorders and Stroke (NINDS)
CollaboratorNIH
Sepulveda Research Corporation
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* ischemic stroke within the past 30 days * transient ischemic attack within the past 30 days * person receiving care at VA Long Beach Healthcare System

Exclusion criteria

* unable to understand informed consent * already enrolled in another research study

Design outcomes

Primary

MeasureTime frame
Blood pressure controlbaseline, 3 months, 7 months

Secondary

MeasureTime frameDescription
patient perceptions of care qualitybaseline, 3 months, 7 months
medication adherencebaseline, 3 months, 7 months
control of other stroke risk factors including lipids, smoking, and exercisebaseline, 3 months, 7 months
Stroke knowledgebaseline, 3 months, 7 monthsOpen ended questions about the warning signs about stroke. Open ended questions about the risk factors of stroke. These questions evaluate the effectiveness of the didactic portion of the group sessions.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026