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临床试验/NCT04307004
NCT04307004已完成不适用

Evaluating Novel Approaches for Estimating Awake and Sleep Blood Pressure - Better BP Study

University of Alabama at Birmingham3 个研究点 分布在 1 个国家目标入组 654 人开始时间: 2019年7月15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
654
试验地点
3
主要终点
Absolute Difference Between Unattended and Attended Blood Pressure

研究概览

简要总结

The purpose of the proposed study is to test whether measuring unattended blood pressure using an automated blood pressure monitor in a clinic setting without staff being present can reduce the need for assessing out-of- clinic awake blood pressure using ambulatory monitoring. Also, the investigators will test whether asleep blood pressure can be accurately measured using a novel home blood pressure monitoring device with less burden compared with ambulatory monitoring.

详细描述

For many people, blood pressure levels differ when measured in a doctor's office versus during normal daily activities. Ambulatory blood pressure monitoring, also called ABPM, involves wearing a blood pressure cuff attached to a device that is programmed to measure participants blood pressure every 30 minutes for a 24-hour period. ABPM can help better estimate a person's true average blood pressure. Although ABPM is recommended for diagnosing high blood pressure and it also measures blood pressure while people sleep, it is not available in many clinics and some people find the procedure to be uncomfortable. The purpose of this research study is to test whether blood pressure measured in a clinic setting without medical staff present is comparable to blood pressure levels measured during the daytime measured using an ABPM device. Also, the investigators will test whether asleep blood pressure can be accurately measured using a home blood pressure monitoring device. These findings may help identify new approaches for diagnosing high blood pressure without the need for ABPM. Each participant will complete four study visits. During the course of the study, participants will:

  • Have their blood pressure measured in the clinic, six times at each of the first two study visits for a total of twelve blood pressure measurements.
  • Complete questionnaires about their demographics, medical history, and participant sleeping habits.
  • Have their blood drawn and provide a urine sample.
  • Wear a Food and Drug Administration-approved ABPM device (Microlife WatchBP O3) for 24 hours.
  • Wear a Food and Drug Administration-approved home blood pressure monitor (Microlife WatchBP Home N) while they sleep for one night.
  • Wear an activity monitor (Actiwatch) for two 24-hour periods. The Actiwatch activity monitor measures activity levels and can be used to identify when they are asleep.
  • Answer some questions about their experience while wearing the ABPM and home blood pressure monitor.
  • Have an echocardiogram performed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
19 Years 至 87 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Mean screening systolic blood pressure of 110 to < 160 mm Hg at most recent visit
  • Mean screening diastolic blood pressure of 70 to <100 mm Hg at most recent visit

排除标准

  • Currently taking antihypertensive medications
  • Known to be currently pregnant
  • History of sleep apnea
  • History of heart attack, stroke, or any cardiovascular disease
  • History of arrhythmia (e.g. - atrial fibrillation or ventricular tachycardia)
  • Completed ambulatory blood pressure monitoring in the past year
  • Second shift, overnight, or jobs that will not allow ambulatory blood pressure device to measure every 30 minutes for 24 hours.

研究组 & 干预措施

ABPM vs HBPM

Other

Participants will be fitted with either the Microlife WatchBP O3 ambulatory blood pressure monitoring device or instructed on how to use the Microlife WatchBP Home N home blood pressure device, depending on which they are assigned to complete first. The order in which participants undergo ambulatory or home blood pressure monitoring will be assigned through a random number generator.

干预措施: Ambulatory blood pressure monitoring (Other)

Unattended vs Attended Blood Pressure

Other

Participants blood pressure will be measured three times attended and three times unattended using the Microlife WatchBP Office AFIB device. Whether investigators measure blood pressure attended first and then unattended or unattended first and then attended will be assigned using a random number generator. At visit 2, clinic blood pressure will be measured three times attended and three times unattended using the Microlife WatchBP Office AFIB device, as at visit 1, but in the reverse order.

干预措施: Unattended blood pressure measurement (Other)

Unattended vs Attended Blood Pressure

Other

Participants blood pressure will be measured three times attended and three times unattended using the Microlife WatchBP Office AFIB device. Whether investigators measure blood pressure attended first and then unattended or unattended first and then attended will be assigned using a random number generator. At visit 2, clinic blood pressure will be measured three times attended and three times unattended using the Microlife WatchBP Office AFIB device, as at visit 1, but in the reverse order.

干预措施: Attended blood pressure measurement (Other)

ABPM vs HBPM

Other

Participants will be fitted with either the Microlife WatchBP O3 ambulatory blood pressure monitoring device or instructed on how to use the Microlife WatchBP Home N home blood pressure device, depending on which they are assigned to complete first. The order in which participants undergo ambulatory or home blood pressure monitoring will be assigned through a random number generator.

干预措施: Home blood pressure monitoring (Other)

结局指标

主要结局

Absolute Difference Between Unattended and Attended Blood Pressure

时间窗: 2 days

The difference between both systolic and diastolic blood pressure measurements when a technician is present versus when they are not present in the room.

Accuracy of Measuring Asleep Blood Pressure Using a Home Blood Pressure Monitor as Compared to Using an Ambulatory Blood Pressure Monitor

时间窗: 2 days

Participants will have their systolic and diastolic blood pressure measured overnight using a home blood pressure monitor and over 24-hours using an ambulatory blood pressure monitor.

Tolerability of Wearing a Home Blood Pressure Monitor Versus an Ambulatory Blood Pressure Monitor: Questionnaires

时间窗: 3 days

Participants will complete questionnaires regarding their experience wearing both the ambulatory and home blood pressure monitors as well as a questionnaire on their willingness to wear the devices again.

次要结局

  • Left Ventricular Mass Index(3 days)
  • Urinary Albumin-to-creatine Ratio(3 days)

研究者

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

Emily B. Levitan

Professor and Vice Chair

University of Alabama at Birmingham

研究点 (3)

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