Postpartum Hypertension Self-Management App (PHSMA) / Postpartum Hypertension / Hypertensive Disorders of Pregnancy (HDP) · Interventional Study
ClinicalTrials.gov · September 11, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a completed but unpublished randomized controlled trial of a postpartum hypertension self-management app in 99 women with hypertensive disorders of pregnancy. The study was designed to assess effects on blood pressure control, perceived stress, postpartum stress, and depression over 6 weeks postpartum, but results are not yet available in this registry record.
Interventional, Randomized, Parallel, Open label, Treatment purpose. Postpartum Hypertension, Hypertensive Disorders of Pregnancy (HDP); Female; age from 20 Years. Intervention: Self-Management App Group. Compared with: Usual Care Group — No Intervention. n = 99. 1 site: Taiwan.
This is a completed but unpublished randomized controlled trial of a postpartum hypertension self-management app in 99 women with hypertensive disorders of pregnancy. The study was designed to assess effects on blood pressure control, perceived stress, postpartum stress, and depression over 6 weeks postpartum, but results are not yet available in this registry record.
This is a registry record only; no efficacy, safety, or outcome data are reported.
The source did not state who this applies to in practice.
This is a completed trial registration with no results posted; the study design and planned outcomes are described but efficacy data are not yet available.
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 (NCT07486375). This is a study registration, not published results. Lead sponsor: National Cheng-Kung University Hospital. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 99 participants (ACTUAL). Conditions: Postpartum Hypertension, Hypertensive Disorders of Pregnancy (HDP). Interventions: BEHAVIORAL: Postpartum Hypertension Self-Management App (PHSMA). Primary outcome measures: Blood Pressure Control , Baseline to 6 weeks postpartum; Perceived Stress , Baseline to 6 weeks postpartum; Postpartum Stress , Baseline to 6 weeks postpartum; Postpartum depression , Baseline to 6 weeks postpartum. Brief summary: Hypertensive disorders of pregnancy (HDP) are a major cause of maternal morbidity and may continue to affect women after childbirth. Effective postpartum self-management is important for controlling blood pressure (BP) and improving overall health. eHealth applications may provide convenient tools to support self-monitoring and promote healthy behaviors. The purpose of this randomized controlled trial is to evaluate the effectiveness of a self-management application for postpartum women with hypertensive disorders of pregnancy (HDP). Participants are randomly assigned to either a self-management app intervention group or a usual care group. The study assesses whether the application improves blood pressure (BP)control, psychological well-being (stress and depression), and health-promoting lifestyle behaviors among postpartum women.
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