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Improve Awarness of Preeclampsia Among Pregnant Women

Awarness of Preeclampsia and Its Associated Factors Among Pregnant Women in Sohag University Hospital

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07805239
Enrollment
160
Registered
2026-09-04
Start date
2026-09-01
Completion date
2027-09-01
Last updated
2026-09-04

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

Conditions

Preeclampsia Awarness

Brief summary

Preeclampsia is a major pregnancy-related hypertensive disorder and a leading cause of maternal and perinatal morbidity and mortality worldwide, particularly in developing regions. Adequate maternal awareness of preeclampsia symptoms and risk factors is crucial for early detection and timely medical intervention. Objectives: This study aims to assess the level of awareness regarding preeclampsia, its warning signs, and its associated risk factors among pregnant women attending the antenatal care (ANC) clinic at Sohag University Hospital, and to identify socio-demographic factors associated with their awareness levels.

Interventions

OTHERQuestionnaire

Data will be collected by the researcher through personal interviews with the PE admitted inpatient at the Obstetric and Gynecology department and those attending outpatient clinic at Sohag University Hospital using standardized questionnaire.

Sponsors

Aya Magdy Mohamed Amin
Lead SponsorOTHER
Sohag University
CollaboratorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Pregnant women aged 18 years or older. 2. women at high risk of PE ( previous history of PE , Diabetes , chronic hypertension , kidney disease , Autoimmune disorders as Antiphospholipid syndrome ). 3. Ability to communicate effectively and provide informed consent, with no cognitive or psychiatric conditions that would interfere with participation or questionnaire completion.

Exclusion criteria

1. Women with severe medical or obstetric emergencies requiring immediate management at the time of data collection. 2. Women with cognitive impairment, severe psychiatric illness, or communication difficulties that prevent reliable completion of the questionnaire. 3. Incomplete questionnaire responses. \-

Design outcomes

Primary

MeasureTime frameDescription
Preeclampsia Knowledge scoreBaseline (at admission to the department or attendance at the outpatient clinic)Assessed using an investigator-administered, validated, close-ended questionnaire covering preeclampsia awareness, risk factors, signs/symptoms, and complications. Each correct response receives 1 point, while incorrect or "don't know" responses receive 0 points. Scores are expressed as percentages and categorized into adequate knowledge (≥60%) and inadequate knowledge (\<60%).

Contacts

CONTACTSalah Roshdy Ahmed, Professor
salahroshdy@yahoo.com+201153008891

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 5, 2026