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临床试验/NCT02898584
NCT02898584已完成不适用

Utilizing Consumer Health Informatics to Support Management of Hypertension by Clinical Pharmacists in Primary Care

University of Michigan2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2016年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
2
主要终点
Change in blood pressure

研究概览

简要总结

The purpose of this research study is to test the feasibility, acceptability, and preliminary effectiveness of the use of a mobile pharmacist-led intervention that incorporates home BP monitoring and medication reminders with patients recruited from a primary care setting, as well as identify challenges and potential solutions to broader implementation of a mobile pharmacist-led home-based BP monitoring intervention in primary care clinics through key stakeholder interviews.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Have a smart phone compatible with mobile intervention
  • Have been previously diagnosed with hypertension
  • Have uncontrolled hypertension (systolic blood pressure > 140 and/or diastolic blood pressure > 90 on repeat measurement)
  • Be under the care of a primary care physician at the recruitment clinic
  • Be taking at least one antihypertensive medication
  • Be English speaking

排除标准

  • Patients under the care of a clinical pharmacist for hypertension management, or under the care of a cardiologist
  • Pregnant patients and anyone with the following unrelated, but serious medical conditions will also be excluded, as they may make blood pressure control difficult or necessitate frequent hospitalization: previous diagnosis of resistant hypertension; steroid dependent asthma or emphysema; cirrhosis or hepatic failure; stage C or D chronic heart failure; stage IV or V chronic kidney disease; and cancer (terminal or undergoing active chemotherapeutic or radiation therapy)
  • Patients with other serious medical conditions (e.g., stroke, dementia) that may affect their ability to self-monitor blood pressure

结局指标

主要结局

Change in blood pressure

时间窗: from baseline to 12 weeks

次要结局

  • Change in medication adherence as measured by the Adherence to Refills and Medications Scale (ARMS)(from baseline to 12 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lorraine Buis

Assistant Professor of Family Medicine, Medical School and Assistant Professor of Information, School of Information

University of Michigan

研究点 (2)

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