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Postpartum Period / Bundle Intervention / Hypertension · Interventional Study
ClinicalTrials.gov · August 12, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a registry record for an ongoing postpartum intervention trial in women with prior preeclampsia, powered to detect changes in blood pressure and weight over 9 months. No results are yet reported; the trial is actively recruiting and outcomes have not been assessed.
Interventional, Randomized, Parallel, Double masking, Prevention purpose. Preeclampsia, Postpartum Period, Hypertension, Cardiovascular Diseases, Overweight, Obesity; Female; age from 18 Years. Intervention: Bundle Intervention. Compared with: Standard Care — No Intervention. n = 356. 2 sites: Sweden.
This is a registry record for an ongoing postpartum intervention trial in women with prior preeclampsia, powered to detect changes in blood pressure and weight over 9 months. No results are yet reported; the trial is actively recruiting and outcomes have not been assessed.
This is a registry record with no reported results; no efficacy, safety, or outcome data are available.
The source did not state who this applies to in practice.
This is a clinical trial registry record describing a planned interventional study with no results reported; enrollment is ongoing and primary outcomes have not yet been assessed.
As stated by the source record.
Quoted from the source exactly as published.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07199283). This is a study registration, not published results. Lead sponsor: Karolinska Institutet. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 356 participants (ESTIMATED). Conditions: Preeclampsia, Postpartum Period, Hypertension, Cardiovascular Diseases, Overweight, Obesity. Interventions: OTHER: Bundle Intervention. Primary outcome measures: Change in systolic (sBP) blood pressure (mmHg) , From baseline to end of study at 9 months follow-up; Change in diastolic blood pressure (mmHg) , From baseline to end of study at 9 months follow-up. 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 pregnancy. The main questions it aims to answer are: * Does the 9-month intervention reduce systolic and diastolic blood pressure? * Does the intervention promote postpartum weight loss? * Does the intervention affect weight and blood pressure depending on early pregnancy BMI? Researchers will compare the bundle intervention to standard care to see if the intervention improves cardiometabolic health and lifestyle outcomes. All participants will attend clinical visits for outcome assessments. Participants in the intervention group will: * Receive online targeted screening and group meetings with study personnel * Use the trial-specific PEPP app to access self-monitoring tools for blood pressure and weight, lifestyle modification, and health education * Follow the intervention in two phases: starting after inclusion (≈8 weeks postpartum) with a Light phase (baseline-3 months) and progressing to an Intensive phase (3-9 months)
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.