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Development and Empirical Study of a Discharge Preparation Service Program for Postpartum Women with Hypertensive Disorders of Pregnancy

Development and Empirical Study of a Discharge Preparation Service Program for Postpartum Women with Hypertensive Disorders of Pregnancy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109823
Enrollment
Unknown
Registered
2025-09-25
Start date
2025-02-10
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

Hypertensive Disorders of Pregnancy

Interventions

Intervention group:1. Formation of a Multidisciplinary Team (MDT): Regular training and case discussions are conducted by members including obstetricians, nurses (coordinators), pharmacists, dietitian
Control group:(1) Routine Inpatient Care: Adherence to the current standard nursing procedures in the obstetric ward, including monitoring of vital signs, observation of the condition, routine medicat

Sponsors

The First People's Hospital of Zhaoqing
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosis of HDP (Hypertensive Disorders of Pregnancy) meets the diagnostic criteria in the "Guidelines for the Diagnosis and Treatment of Hypertensive Disorders of Pregnancy (2020)" [19]: Hypertension first appearing after 20 weeks of gestation, with systolic blood pressure >=140 mmHg (1 mmHg = 0.133 kPa) and/or diastolic blood pressure >=90 mmHg; negative urine protein test. Severe hypertensive disorder of pregnancy is defined as systolic blood pressure =160 mmHg and/or diastolic blood pressure >=110 mmHg. 2. Informed consent and voluntary participation in this study. 3. Good language communication and comprehension abilities, no consciousness disorders, and able to answer questions.

Exclusion criteria

Exclusion criteria: 1. Patients who have other chronic diseases or severe organic diseases during hospitalization, such as malignant tumors, heart disease, etc. 2. Patients with a history of mental illness and cognitive impairment. 3. Patients who have developed severe complications before childbirth, such as complete placental abruption, HELLP syndrome, etc. 4. Patients who are participating in other similar clinical intervention research projects during hospitalization.

Design outcomes

Primary

MeasureTime frame
Blood pressure control rate;Unplanned readmission rate;

Secondary

MeasureTime frame
Maternal discharge readiness;Quality of obstetric discharge guidance;Incidence of postpartum depression;

Countries

China

Contacts

Public ContactHe Yunping

The First People's Hospital of Zhaoqing

1018823851@qq.com+86 152 1843 8891

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026