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Birth plan and fear of childbirth, self-efficacy and childbirth experiences in primiparous women

Investigating the effect of implementing a birth plan on fear of childbirth, self-efficacy and childbirth experiences among Primiparous Women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110621006854N7
Enrollment
65
Registered
2023-04-20
Start date
2023-03-11
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

None listed

Interventions

Intervention 1: At first, researcher explained the importance and method of writing the birth plan to the participants, and then they will write the birth plan, which includes writing down the des

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Being in the age range of 18 to 45 years Being Iranian Having a first child Being in the range of 28 to 41 weeks of pregnancy Having singleton and low-risk pregnancy Wanted pregnancy literacy and understanding of Persian language Desire to give birth in hospitals affiliated to Tehran University of Medical Sciences

Exclusion criteria

Exclusion criteria: Participating in another study Pregnancy being complicated

Design outcomes

Primary

MeasureTime frame
Fear of childbirth(primary outcome). Timepoint: 1At the end of the intervention and 4-6 weeks after delivery. Method of measurement: Questionnaires of fear of childbirth.;Childbirth self efficacy(Secondary outcome). Timepoint: Immediately after finishing the study. Method of measurement: vijma standard questionnaire.;Childbirth satisfaction(secondary outcome). Timepoint: after finishing the study. Method of measurement: standard questionnaire of childbirth satisfaction.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Ebrahimi

Tehran University of Medical Sciences

ebrahimi_308@yahoo.com+98 912 646 4211

Outcome results

None listed

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