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临床试验/NCT03116815
NCT03116815已完成不适用

The Feasibility of a Web-based Application to Monitor Home Blood Pressure

Loyola University2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2017年5月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
试验地点
2
主要终点
The total number of patients who provide written informed consent to participate in the study

研究概览

简要总结

Control of hypertension remains one of the most important interventions available to clinicians to reduce risk of cardiovascular disease, kidney disease and stroke. Self-measured home blood pressure monitoring plus additional support has been shown to reduce blood pressure in adults with previously uncontrolled hypertension. Most previous studies have utilized healthcare personnel to facilitate communication of home blood pressure levels to physicians and did not provide methods to directly transmit self-measured blood home blood pressure levels to physicians via the electronic health record. Emerging technology now provides the ability for patient's to upload self-measured blood pressure levels into their own medical record which may eliminate the need for additional health personnel. This study will examine the feasibility, patient adherence and physician and patient perceptions of a web-based application which will facilitate direct input of self-measured home blood pressure levels and patient reported symptoms directly into the electronic health record with message alerts to the provider for hypertension management. Up to 10 Loyola primary care physicians and 20 of their respective patients age 50 years and older who have a smart phone device or home computer and have treated hypertension will be enrolled. The study will utilize the existing web-application called MyChart. MyChart is the name of the web-based application and it is not an acronym. Enrolled patients will download the existing MyChart web-based application on their smart phone device or home computer and will record home blood pressure measurements using their home blood pressure machine into their smart phone application. The MyChart application is available to all patients receiving care in the Loyola Health Care System. The blood pressure readings and patient reported symptoms will then be available for their physicians to review within the electronic health record. After using the web-based application for two months, both patients and physicians will be asked to participate in focus groups and interviews, respectively, to determine their perceptions and satisfaction with the web-based application. Data from this feasibility study may be used to guide a future clinical trial of hypertension management that examines the effectiveness of the MyChart web-based application for frequent blood pressure monitoring compared to standard care.

详细描述

Observational studies and clinical trials have demonstrated that clinicians fail to intensify therapy in hypertensive management despite patients not meeting goal. For this reason, patient centered tools can help facilitate meeting goals with the provider. Web-based communication combined with provider care management successfully lowered blood pressure to <140/90 mm Hg in prior studies of patients with hypertension. Emerging technology now provides the ability for patients to upload self-measured home blood pressure information into their own medical record which may eliminate the need for additional health personnel. This study will investigate the feasibility of health informatics to facilitate better compliance and safety for both provider and patient for hypertension management. The home blood pressure readings along with patient reported symptoms will be recorded using the MyChart, a web-based tool available to all patients receiving care at Loyola University Medical Center. MyChart can be accessed with a hand-held device or home computer. After enrollment, patients will receive a notice every two weeks via MyChart to upload home blood pressure values and patient reported symptoms. This information entered into MyChart by patients will be placed into the electronic health record in a home vital signs flow sheet, which will be separate from the flow sheet of vital signs measured in the clinic. Physicians will receive an alert message when patients upload the blood pressure data. The alert message will provide physicians with the average blood pressure value over the two weeks and will provide simple guidance on whether actions, such as titrating existing medication should be taken (based on whether BP is ≥ 140/90 mmHg). Patients will also be able to track their own home blood pressure values using the MyChart application. As a first step, we are first examining the feasibility of this web-based application and determining the perceptions of both patients and physicians.

研究设计

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

入排标准

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

入选标准

  • Inclusion Criteria:
  • Willing to participate in all study procedures
  • Potential subject owns a personal device and is able to run the web-application
  • Physician directed blood pressure goal is < 140/90 mmHg

排除标准

  • No use of blood pressure lowering medications
  • Arm circumference too large or small to allow accurate blood pressure measurement
  • A medical condition likely to limit survival to less than 6 months, or a cancer diagnosed and treated within the past two years that, in the judgment of clinical study staff, would compromise a participant's ability to complete the study
  • Inability to give informed consent
  • History of systolic heart failure (ejection fraction < 35%)
  • History of stroke
  • History of proteinuria ≥ 1 gram in a 24 hour urine collection or a random urine albumin/creatinine ratio ≥ 300 mg/g or a random urine protein/creatinine ratio ≥ 300 mg/g

结局指标

主要结局

The total number of patients who provide written informed consent to participate in the study

时间窗: 30 days

The total number of patients who enroll in the study and provide written informed consent

Adverse events

时间窗: 60 days

Total number of patient reported adverse events and all hospitalizations and emergency room visits

Patient reported outcomes

时间窗: 60 days

The percentage quality of life questionnaires completed by the study participants

The total number of patients screened for the study

时间窗: 30 days

The total number of patients who were examined for study eligibility

Change in systolic blood pressure

时间窗: 60 days

Change in systolic blood pressure

The total number of patients who meet study eligibility

时间窗: 30 days

The total number of patients who are screened for the study and meet study eligibility

The number of home blood pressure readings submitted by patients to the MyChart web-based application

时间窗: 60 days

The actual number of home blood pressure readings that are recorded in the electronic health record as submitted via MyChart

Change in diastolic blood pressure

时间窗: 60 days

Change in diastolic blood pressure

Correlation between office and home blood pressure readings

时间窗: one day

Correlation between the office blood pressure measurement using the clinic Omron machine and the patient's home blood pressure cuff

Physician actions based on home blood pressure readings

时间窗: 60 days

Total number of times a physician escalates or de-escalates blood pressure lowering medications for a study participant

次要结局

未报告次要终点

研究者

发起方
Loyola University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Holly J. Mattix-Kramer

Professor

Loyola University

研究点 (2)

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