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Educational and Counseling Program for Pregnant Women at Risk of Preeclampsia

Assessing the Effects of an Education and Counseling Program on Health-Promoting Lifestyle in Pregnant Women at Risk of Preeclampsia

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221109056451N4
Enrollment
108
Registered
2024-10-09
Start date
2024-09-30
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

O14 is "Preeclampsia.". Health-promoting lifestyle aspects are not classified under ICD-10 codes and will not be documented.

Interventions

Intervention 1: Control group: Pregnant women in the control group receive standard and routine prenatal care. Intervention 2: Intervention group:.

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Pregnant women should be between 12 to 16 weeks of pregnancy. Be at risk for preeclampsia (at least one high-risk factor or at least two moderate-risk factors). Have the ability to read and write in Persian. Be willing to participate in the research.

Exclusion criteria

Exclusion criteria: Lack of planning for follow-up care and delivery in the hospital indicates. Unwillingness to continue participation in the research.

Design outcomes

Primary

MeasureTime frame
Improvement in health-promoting lifestyle scores. Timepoint: Data will be collected at two points: Baseline (12-16 weeks): Assessment of lifestyle behaviors. Follow-up (35-40 weeks): Evaluation of pregnancy-induced hypertension (PIH) and maternal-fetal outcomes through medical records. Method of measurement: Assessment of lifestyle behaviors using Health-Promoting Lifestyle Questionnaire by Walker and colleagues.

Secondary

MeasureTime frame
Evaluation of pregnancy-induced hypertension. Timepoint: At the time of delivery and the postpartum period. Method of measurement: Medical records.;Maternal-fetal outcomes through medical records. Timepoint: At the time of delivery and the postpartum period. Method of measurement: Medical records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Bakouei

Babol University of Medical Sciences

bakouei2004@yahoo.com4717647745

Outcome results

None listed

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