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临床试验/NCT03228082
NCT03228082已完成不适用

Blood Pressure After PREeclampsia/HELLP by SELF Monitoring

Radboud University Medical Center6 个研究点 分布在 2 个国家目标入组 200 人开始时间: 2017年7月13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
200
试验地点
6
主要终点
Feasibility of HBPM after a previous preeclampsia to evaluate the prevalence of hypertension.

研究概览

简要总结

RATIONALE:

Women with a previous history of preeclampsia (PE)/HELLP have a twofold higher risk of cardiovascular disease (CVD) and a fourfold increased risk to develop hypertension at a relative young age. In the latest 2016 ESC guidelines 'CVD prevention', previous PE has been acknowledged as a serious CVD risk factor in women. In clinical practice, however, these women are still underappreciated for their CVD risk. It has not been established yet how adequate lifelong prevention in these potentially high risk women can optimally be achieved from their childbearing years onwards.

OBJECTIVE:

To evaluate feasibility, usability, acceptance and potential obstacles of blood pressure (BP) home monitoring in high-risk women, aged 40-60 years, after a previous PE in pregnancy. In addition to evaluate the effectiveness of BP home monitoring on the occurrence of hypertension, the efficacy of BP treatment, quality of life (QOL), health-related symptoms, work ability and life-style behaviour.

STUDY DESIGN:

Randomized, open label feasibility study to compare eHealth guided self management of BP monitoring and lifestyle advice with 'usual care'.

STUDY POPULATION:

Approximately 200 women, aged ≥ 40 and ≤ 60 years, with a previous PE in pregnancy will be invited to participate (both early and late PE). Patients will be recruited from the departments of obstetrics/gynaecology in 6 centres in the Euregio Rhein-Waal and from the department of cardiology Radboudumc.

INTERVENTION:

eHealth guided measurements of BP at regular intervals and recurrent lifestyle advice (intervention-group) will be compared with "usual care".

PRIMARY OUTCOME:

Feasibility, usability, acceptance and potential obstacles of BP home monitoring in high-risk women after a previous PE in pregnancy at 1 year of follow-up.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Device Feasibility
盲法
None

入排标准

年龄范围
40 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •previous preeclampsia/HELLP syndrome, defined as diastolic BP≥90 mmHg with proteinuria ≥ 0.3gram/24 h, during one or more pregnancies, more than 1 year ago.
  • •'early' or 'late' PE/HELLP
  • •age ≥40 and ≤ 60 years

排除标准

  • •pregnant women or women wishing for future pregnancie(s)
  • •inability to perform self BP measurements
  • •not having a smartphone (Apple or Android)
  • •already having regular hypertension control by GP or medical specialist
  • •previous cardiovascular events, such as myocardial infarction , stroke, heart failure and symptomatic ischemic heart disease

研究组 & 干预措施

Home Blood Pressure Monitoring (HBPM)

Experimental

Home monitoring of blood pressure will be performed. Blood pressure measurements will be entered automatically through a smartphone application into a patient-controlled medical record ('Patients Know Best'). The data will be available to the study coordinator, who will provide patients within 1 week with feedback on the measurements. If necessary lifestyle advice will be given, in case of hypertension patients will be referred to their GP.

Once monthly a questionnaire on well-being (SF-12) and symptoms will be completed. After 6 months and 1 year patients will also receive a questionnaire on feasibility and usability of the blood pressure device.

干预措施: Home Blood Pressure Monitoring (HBPM) (Device)

Control group

No Intervention

Patients in the control group will be asked to register their blood pressure if measured during a doctor's visit, and to note medication use if applicable. They will also be asked to complete a short questionnaire on well-being (SF-12) once per month, which will be evaluated at the end of the study. No interim contact with the study coordinator is scheduled.

结局指标

主要结局

Feasibility of HBPM after a previous preeclampsia to evaluate the prevalence of hypertension.

时间窗: 1 year

To evaluate feasibility of blood pressure home monitoring to diagnose hypertension at 1 year follow-up, in high-risk women with a previous preeclampsia. Feasibility will be measured using questionnaires (Likert scales).

次要结局

  • Blood pressure values(1 year)
  • Effect HBPM(1 year)
  • Prevalence of hypertension(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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