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BloodPressure after PREeclampsia/HELLP by SELF monitoring study

BloodPressure after PREeclampsia/HELLP by SELF monitoring study - BP-PRESELF study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON43149
Enrollment
300
Registered
2017-05-08
Start date
2017-06-13
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hoge bloeddruk elevated blood pressure hypertension

Interventions

eHealth guided measurements of BP at regular intervals and recurrent lifestyle advice will be compared with *usual care*.

Sponsors

cardiologie
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to be eligible for participation in this study, a subject must meet all of the following criteria: - 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

Exclusion criteria

Exclusion criteria: -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

Design outcomes

Primary

MeasureTime frame
Mean systolic and diastolic BP levels, prevalence of hypertension and medication use for hypertension at baseline, during study period and after 1 year of follow-up

Secondary

MeasureTime frame
- QOL measures (questionnaires) - ability to work and work-related obstacles - cardiac/ hypertensive symptoms and well-being - cost-effectiveness and feasibility of BP self monitoring program

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)