Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
100 participants
INTERVENTIONAL
2006-09-30
2007-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Control
assisted appointment with physician
Parish nurse visit
One visit with the parish nurse in 2 weeks
Interventions
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Parish nurse visit
One visit with the parish nurse in 2 weeks
Eligibility Criteria
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Inclusion Criteria
* Patients must be either English or Spanish speaking.
* Patients will be enrolled by blood pressure readings at the screening event. We will be using the JNC 71 criteria for diagnosing hypertension.
* Patients with blood pressures above 140/90 will be defined as hypertensive.
* Diagnosed and previously undiagnosed hypertensive patients will be included in the study.
* The patient must also be able to come to the follow-up appointment in 4 months.
Exclusion Criteria
* Patients who do not speak English or Spanish will be excluded from the study since we do not have the capacity to translate all our materials into multiple languages.
* Those deemed by the research assistant to be incapable to give informed consent (due to intoxication, dementia, or other causes) will also be excluded from the study.
* Patients younger than 18 years old will be excluded from the study.
* Patients who have seen a parish nurse in her office hours in the past 6 months will be excluded from the study. We do not want patients who have an already established relationship with a parish nurse to be enrolled in the study with the chance of being randomized to the physician-only arm, which would interrupt the continuity of care the patient is receiving from the parish nurse.
18 Years
ALL
No
Sponsors
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Robert Wood Johnson Foundation
OTHER
University of California, Los Angeles
OTHER
Principal Investigators
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Arshiya A Baig, MD/MPH
Role: PRINCIPAL_INVESTIGATOR
UCLA RWJ CSP
Other Identifiers
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#G06-08-103-02A
Identifier Type: -
Identifier Source: org_study_id
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