Biopsychosocial model |
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Clinical Trial: A Team Model of Hypertension Care in African Americans
This study is not yet open for patient recruitment.
Verified by University of Wisconsin September 2005
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Purpose
This study will evaluate the cost-effectiveness of an organizational-level intervention in a randomized controlled trial involving 900 treated hypertensive African American patients in the Milwaukee and Chicago areas. The study will involve 36 community pharmacies (18 intervention, 18 control) owned by a pharmacy corporation that operates over 2,000 pharmacies nationwide. The intervention will include: a) redefinition of pharmacist and pharmacy technician roles, b) implementation of a pharmacy-based “refill clinic” and tools for enhanced monitoring and collaboration with patients and physicians, and c) special training/certification of pharmacy personnel in blood pressure measurement, collaborative skills, and cultural competency.
| Condition | Intervention |
|---|---|
| hypertension in African Ammericans | Behavior: educational |
MedlinePlus consumer health information
Study Type: Interventional
Study Design: Educational/Counseling/Training, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study
Further Study Details:
Primary Outcomes: the cost-effectiveness of an organizational-level intervention in treating hypertensive African Americans in Milwaukee and Chicago
Secondary Outcomes: how did the intervention affect the process of care (including pharmacists behavior, patient-reported barriers, prescribed regimens, patient adherence)
Expected Total Enrollment: 900
Secondary Outcomes: how did the intervention affect the process of care (including pharmacists behavior, patient-reported barriers, prescribed regimens, patient adherence)
Expected Total Enrollment: 900
Study start: September 2005
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
- african american
- 18 y/o or older
- obtain all prescribed drugs at the study pharmacy
Exclusion Criteria:
- history of organ transplant
- kidney dialysis
- terminal illness
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00205153
Bonnie L Svarstad, PhD 608-265-2128 blsvarstad@pharmacy.wisc.edu
Wisconsin
University of Wisconsin, Madison, Wisconsin, 53792, United States
Bonnie L Svarstad, PhD 608-265-2128 blsvarstad@pharmacy.wisc.edu
Study chairs or principal investigators
Bonnie L Svarstad, PhD, Principal Investigator, University of Wisconsin
More Information
Study ID Numbers: M-2000-0284; NIH R01 HL78580
Last Updated: September 19, 2005
Record first received: September 13, 2005
ClinicalTrials.gov Identifier: NCT00205153
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-09-20
Last Updated: September 19, 2005
Record first received: September 13, 2005
ClinicalTrials.gov Identifier: NCT00205153
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-09-20

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