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临床试验/NCT03291535
NCT03291535已完成不适用

Virtual Hypertension Management Pilot: Randomized Evaluation of Electronic Health Record-connected Blood Pressure Cuffs in a Clinical Pharmacist Panel.

Stanford University2 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2017年7月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
75
试验地点
2
主要终点
Change in blood pressure over time in control group vs. the intervention group

研究概览

简要总结

Investigators are examining the quality improvement impact of providing patients with a an electronic health record-connected blood pressure cuff. Investigators will give half of patients already eligible for hypertension management within a clinical pharmacist panel, the ability to upload their blood pressure data into Stanford's electronic health record.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • •Hypertension as defined by clinical pharmacist usual care panel (2 or more readings of blood pressure >140/90)

排除标准

  • •Pregnancy
  • •Chronic kidney disease III or IV
  • •Systolic heart failure with ejection fraction <35%
  • •Current use of 3 or more anti-hypertension drugs

研究组 & 干预措施

Control

Placebo Comparator

This arm will consist of the usual care of management of hypertension by a clinical pharmacist.

干预措施: Usual care (Other)

Intervention

Active Comparator

This arm will consistent of usual care plus the addition of a blood pressure cuff that will allow patients to upload data to the electronic health record via a secure portal.

干预措施: Connected-device (Other)

结局指标

主要结局

Change in blood pressure over time in control group vs. the intervention group

时间窗: From enrollment to 6 months later

Difference in the change in blood pressure between the control group and intervention group.

次要结局

  • Blood pressure control(From enrollment to 6 months later)
  • Patient remote interactions(From enrollment to 6 months later)
  • Medication changes(From enrollment to 6 months later)
  • Patient visits(From enrollment to 6 months later)

研究者

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

N. Lance Downing, MD

Clinical Assistant Professor of Medicine

Stanford University

研究点 (2)

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