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Awareness, Preconception, and Fear of Epidural Analgesia Among Childbearing Women in Saudi Arabia.

Awareness, Preconception, and Fear of Epidural Analgesia Among Childbearing Women in Saudi Arabia.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05596604
Enrollment
202
Registered
2022-10-27
Start date
2022-08-01
Completion date
2022-10-10
Last updated
2022-10-27

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

Conditions

Assess Women Awareness and Fear About EDA for Labor

Keywords

Awareness, preconception, fear, epidural analgesia, labor pain

Brief summary

The aim of our study is to measure the level of awareness, preconceptions, and level of fear regarding epidural analgesia among childbearing women in KKUH in Riyadh.

Detailed description

This research was designed as a hospital-based observational cross-sectional study conducted at King Khalid University Hospital, using a self-administered questionnaire based on previous research.22-24-26 approved by the Institutional Review Board at King Saud University, College of Medicine, Riyadh, Saudi Arabia on 08.August.2022 Ref. No. 22/0592/IRB. The sample included pregnant women attending an obstetrical clinic for routine antenatal follow-up, and the data collection was conducted during the month of August 2022. The questionnaire included five parts (sociodemographic, preconception, awareness, fear, and desirability). a total of 26 questions with multiple-choice answers. The sample size was determined using the Comrey and Lee criterion Comrey and Lee (1992) stated that a 200-sample size is acceptable. The questionnaire was completed by 202 participants who met the inclusion criteria that is being a pregnant woman and completing the survey, and the exclusion criteria were non-pregnant women and an incomplete survey. The data collectors made it clear to the participants that taking part in the study was completely optional, and the participants signed anonymous consent forms.

Interventions

OTHERsurvey- no intervention

survey- no intervention

Sponsors

King Saud University
CollaboratorOTHER
King Khalid University Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* pregnant woman * completing the survey

Exclusion criteria

* non-pregnant women * incomplete survey

Design outcomes

Primary

MeasureTime frameDescription
Awarenessmonthassess awareness among participants

Countries

Saudi Arabia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026