Status:

NOT_YET_RECRUITING

The PreEclampsia Postpartum Prevention Trial

Lead Sponsor:

Karolinska Institutet

Conditions:

Preeclampsia

Postpartum Period

Eligibility:

FEMALE

18+ years

Phase:

NA

Brief Summary

The goal of this clinical trial is to learn if a postpartum bundle intervention can improve cardiometabolic health and lifestyle-related factors in women who have had preeclampsia during their first p...

Detailed Description

PURPOSE AND AIMS: The overall aim of this 9-month multicentre, two-arm, single-blind, parallel-group RCT across several regions in Sweden is to improve cardiometabolic health in women after a first p...

Eligibility Criteria

Inclusion

  • Inclusion Criteria
  • First-time mothers postpartum
  • Preeclampsia during first pregnancy
  • Age ≥ 18 years
  • Singleton live birth (infant still alive)
  • Ability to understand and speak Swedish, English, Arabic, Somali, Dari, Persian, or Spanish
  • Having a smartphone (Android or iOS)
  • Ability to provide informed consent
  • Exclusion Criteria:
  • Pre-pregnancy hypertension
  • Diabetes mellitus type I or II
  • Cardiovascular disease
  • Kidney disease
  • Systemic lupus erythematosus
  • Antiphospholipid syndrome
  • Previous or current eating disorders
  • Ongoing new pregnancy

Exclusion

    Key Trial Info

    Start Date :

    November 1 2025

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ESTIMATED

    End Date :

    May 1 2029

    Estimated Enrollment :

    760 Patients enrolled

    Trial Details

    Trial ID

    NCT07199283

    Start Date

    November 1 2025

    End Date

    May 1 2029

    Last Update

    September 30 2025

    Active Locations (1)

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    Karolinska Institutet

    Stockholm, Stockholm County, Sweden, 17177