Education for first-time pregnant women with fear of childbirth
The Effects of Education Given to Primiparous Pregnant Women Who Have Fear of Childbirth According to Joyce Travelbee's Human-to-Human Relationship Model on Fear of Childbirth, Readiness for Childbirth and Acceptance of the Maternal Role
This study is testing if educational support can help first-time pregnant women who are afraid of childbirth feel more prepared and confident about becoming mothers.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 70 (estimated) |
| Sex | Female |
| Sponsor | Hasan Kalyoncu University Academic / other |
| Locations | 1 site (Kilis, Merkez) |
| Trial ID | NCT06947369 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effects of educational interventions based on Joyce Travelbee's Human-to-Human Relationship Model on first-time pregnant women experiencing fear of childbirth. Conducted as a randomized controlled experimental study, it will involve collecting data from participants at Kilis Prof.Dr.Alaeddin Yavaşca State Hospital between March and July 2025. The study will assess changes in fear of childbirth, readiness for childbirth, and acceptance of the maternal role among the participants. Various assessment tools, including the Wijma Birth Anticipation/Experience Scale, will be utilized to measure outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are first-time pregnant women between 28-40 weeks of gestation who experience a moderate to high level of fear regarding childbirth.
Not a fit: Patients who may not benefit from this study include those with chronic health issues, high-risk pregnancies, or those who have received infertility treatment.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce fear of childbirth and improve maternal readiness and acceptance of the maternal role for first-time mothers.
How similar studies have performed: Other studies have shown positive outcomes with educational interventions for pregnant women, suggesting that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria:1. The pregnant woman's first pregnancy. 2. A mid-level or above score on the Wijma Childbirth Expectation/Experience Scale Version A. 3\. The pregnant woman is between 28-40 weeks of gestation (third trimester). 4. The pregnant woman does not have a chronic health problem. 5. The pregnant woman has a single fetus. 6. The pregnant woman has not received infertility treatment. 7. The pregnant woman has not received a psychiatric diagnosis. 8. The pregnant woman does not have a high-risk pregnancy. 9. The pregnant woman's acceptance to participate in the study. Exclusion Criteria:1. Not willing to participate in the study 2. Not speaking Turkish 3. Illiterate, having communication difficulties 4. Not meeting the study criteria \-
Where this trial is running
Kilis, Merkez
- Kilis Prof.Dr.Alaeddin Yavaşca State Hospital — Kilis, Merkez, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Funda G BİLGEN
- Email: fundabilgen@kilis.edu.tr
- Phone: +905052381003
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.