Effect of Self-care on the Pregnancy Outcome of Women with Blood Pressure Disorders

Investigating the Effect of the Self-care Training Program Based on the Empowerment Model on the Pregnancy Outcomes of Women with Blood pressure Disorders

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20241013063351N1

Enrollment

100

Registered

2024-11-18

Start date

2024-11-21

Completion date

Unknown

Last updated

2025-01-08

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

Conditions

Blood pressure disorders of pregnancy. Z35-Supervision of high-risk pregnancy

Interventions

Intervention 1: intervention group : women with hypertension disorders will receive self - care educational intervention ( including physical , mental , spiritual self - care , etc. ) depending on the

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Gestational Hypertension and Women at Risk of Preeclampsia Single Pregnancy A Healthy Live Fetus Age 18-45 Years Gestational Age 20 to 30 Weeks Low score of self-care knowledge and performance questionnaire Willingness and Written Consent to Participate in the Research Project Have Physical and Mental Ability to Take Care of Themselves.

Exclusion criteria

Exclusion criteria: Withdrawal From the Study Having Other Pregnancy Complications (Bleeding, Gestational diabetes, etc.) Having Other Chronic Disorders (Asthma, Epilepsy, Diabetes, Heart disease, Thyroid disorders, etc.)

Design outcomes

Primary

Measure	Time frame
Improving self-care behaviors (knowledge score and self-care performance in a researcher-made questionnaire). Timepoint: Before the study and 4 weeks after the intervention. Method of measurement: Researcher-made questionnaire for self-care knowledge and practice.	—

Secondary

Measure	Time frame
Adherence to Treatment. Timepoint: 4 Weeks after the Intervention. Method of measurement: The Questionnaire was Developed by the Researcher.;Number of prenatal care. Timepoint: 4 Weeks after the Intervention. Method of measurement: Questionnaire.;Blood pressure control. Timepoint: At the beginning of the intervention and daily for up to one week after diagnosis and then every week until the end of the intervention. Method of measurement: Sphygmomanometer.;Number of hospitalizations. Timepoint: 4 Weeks after the Intervention. Method of measurement: Questionnaire.;Length of hospitalization. Timepoint: 4 Weeks after the Intervention. Method of measurement: Questionnaire.	—

Measure

Time frame

Adherence to Treatment. Timepoint: 4 Weeks after the Intervention. Method of measurement: The Questionnaire was Developed by the Researcher.;Number of prenatal care. Timepoint: 4 Weeks after the Intervention. Method of measurement: Questionnaire.;Blood pressure control. Timepoint: At the beginning of the intervention and daily for up to one week after diagnosis and then every week until the end of the intervention. Method of measurement: Sphygmomanometer.;Number of hospitalizations. Timepoint: 4 Weeks after the Intervention. Method of measurement: Questionnaire.;Length of hospitalization. Timepoint: 4 Weeks after the Intervention. Method of measurement: Questionnaire.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNehbandani Sanaz

Ahvaz University of Medical Sciences

snehbandani2013@gmail.com+98 61 3311 0000

Outcome results

None listed

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