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临床试验/NCT00626041
NCT00626041Unknown不适用

U-CHAMP: Urban Cardiovascular Health Assessment and Management Program

University of Calgary4 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2008年2月最近更新:
适应症

试验速览

阶段
不适用
入组人数
110
试验地点
4
主要终点
Change in systolic blood pressure between baseline (average of visits one and two) and program end (final visit).

研究概览

简要总结

High blood pressure, elevated blood glucose and high cholesterol are related to the increased risk of stroke and heart disease. Many studies have shown that this risk can be significantly reduced by lowering blood pressure, blood glucose and cholesterol levels.

Through a collaborative effort between Calgary Safeway pharmacists and Calgary Health Region family physician PCN's, U-CHAMP will deliver a program to assist in the identification and management of people with elevated blood pressure, blood glucose and cholesterol and through this effort, reduce the risk of heart disease and stroke in the urban Calgary population aged 18-85 years.

详细描述

Hypertension (HBP) has long been correlated with risk of stroke and other adverse cardiovascular outcomes. Randomized controlled trials of blood pressure lowering have demonstrated at least 30% reductions in stroke incidence and improved mortality. Despite being such a readily modifiable risk, HBP remains under diagnosed and under treated. To address this gap, the A-CHAMP (Airdrie Community Hypertension Awareness and Management Program) was successfully piloted in Airdrie, a community of 20,000 north of Calgary, Alberta. Trained volunteers held BP screening sessions for seniors in local pharmacies and referred hypertensive participants to their GP's and trained pharmacists for blood pressure management. Of the 408 screened participants (40% of all Airdrie seniors), 36.5% had uncontrolled HBP. By program end, systolic BP was decreased by 16.8 mm (+/- 14.6. P <.05) and 56.2% of hypertensive participants had reached the 2006 Canadian Hypertension Guideline targets. Airdrie now holds annual blood pressure screenings organized and run by volunteers, demonstrating the sustainability of this approach to population screening and risk factor management in this setting.

In order to fully realize the benefits of cardiovascular risk reduction, U-CHAMP will be expanded to include a more global risk assessment and management protocol including assessments for dyslipidemias and diabetes in an urban setting.

The purpose of this project is:

  • To expand the rural scope of A-CHAMP into a larger urban setting (Calgary).
  • To include a more global risk assessment (for both coronary artery disease and stroke) and management including: cholesterol (total and HDL cholesterol) and diabetes (capillary HgA1c when appropriate).
  • To effect fully sustainable practice change in the management of hypertension, diabetes and dyslipidemias by establishing collaborative partnerships between pharmacists, Calgary Health Region (CHR) physicians (Primary Care Networks: PCN's), the CHR Chronic Disease Management Program (CDM), and selected hypertensive patients.

Components of U-CHAMP are as follows:

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Screening
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults 18-85 years
  • Signed consent

排除标准

  • 未提供

结局指标

主要结局

Change in systolic blood pressure between baseline (average of visits one and two) and program end (final visit).

时间窗: 12 months

次要结局

  • Proportion of screened participants identified as being above blood pressure, cholesterol and blood glucose targets at visit two(12 months)
  • Proportion of participants that achieve published blood pressure (lipid and diabetes when appropriate) targets by program end(12 months)
  • Proportion of individuals that obtain both a baseline and end of program full lipid panel(12 months)
  • Change in Framingham Global Cardiovascular Risk score (in those participants that do not have known vascular disease or diabetes and have a recorded baseline and end-of-study full lipid panel).(12 months)
  • Proportion of individuals that have changes in drug therapy (new medication and/or dosage increase).(12 months)

研究者

申办方类型
Other

研究点 (4)

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