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The BP2 (Blood Pressure Postpartum) study: a 3-arm, randomised trial of follow-up and lifestyle behaviour change strategies in the first 12 months after hypertensive disorders of pregnancy

Not Applicable
Completed
Conditions
Preeclampsia
Gestational Hypertension
Chronic Hypertension in pregnancy
Cardiovascular - Hypertension
Public Health - Health promotion/education
Reproductive Health and Childbirth - Fetal medicine and complications of pregnancy
Registration Number
ACTRN12618002004246
Lead Sponsor
Dr Amanda Henry
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
484
Inclusion Criteria

Have given birth at one of the study hospitals during the study period.
The index pregnancy was complicated by a hypertensive disorder of pregnancy: preeclampsia (PE), gestational hypertension (GH), chronic hypertension ± superimposed PE

Exclusion Criteria

Plan to move out of study area/known unavailability to follow-up during study period
Active severe mental health condition or developmental disability precluding informed consent.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in systolic blood pressure measured using the average of three measurements from a validated automated blood pressure device; the Omron HEM-907<br><br><br>[At 12 months postpartum (comparison between 6 month and 12 months postpartum values).];Maternal lifestyle behaviour change (LBC) as assessed by decrease in weight (4kg or more) measured by research staff using digital scales.[At 12 months postpartum (comparison between 6 month and 12 months postpartum values).<br><br>];Maternal lifestyle behaviour change (LBC) as assessed by a decrease in waist circumference (2cm or more) measured with a measuring tape around the narrowest part of the torso.<br>[At 12 months postpartum (comparison between 6 month and 12 months postpartum values).]
Secondary Outcome Measures
NameTimeMethod
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