Training with Pecha Kucha to reduce anxiety and improve birth satisfaction in first-time pregnant women
The Effect of the Training Given Using the Pecha Kucha Technique on the Anxiety and Birth Satisfaction of the First Pregnant Women Followed in Labor.
NA · Kocaeli University · NCT06435988
This study tests whether a special training program can help first-time pregnant women feel less anxious and more satisfied with their birth experience.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 45 Years |
| Sex | Female |
| Sponsor | Kocaeli University (other) |
| Locations | 1 site (Gebze, Kocaeli̇) |
| Trial ID | NCT06435988 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of Pecha Kucha training on anxiety levels and birth satisfaction among first-time pregnant women. A total of 50 participants will be randomly assigned to either an experimental group receiving the training or a control group. The training aims to provide structured birth information to help manage anxiety and enhance the overall birth experience. After the intervention, participants will complete surveys assessing their satisfaction and anxiety levels related to childbirth.
Who should consider this trial
Good fit: Ideal candidates for this study are first-time pregnant women aged 18 and over who are in the latent phase of labor and do not have perinatological risks.
Not a fit: Patients who are in the active phase of labor or have any obstetric complications may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce anxiety and improve birth satisfaction for first-time mothers.
How similar studies have performed: While the specific use of Pecha Kucha in this context may be novel, similar educational interventions have shown promise in reducing anxiety and improving patient satisfaction in other healthcare settings.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Primary pregnant women, * Pregnant women aged 18 and over, * Pregnant women in the latent phase of labor * Pregnant women who do not have perinatological risk, * Pregnant women who can understand and speak Turkish Exclusion Criteria: * • Risky pregnant women, * Pregnant woman in active phase, * Pregnant women who develop an obstetric complication during labor follow-up (Fetal distress, Cord prolapse, Uterine hyperstimulation, non-progressive labor, malpresentation, etc.). * There is a problem that prevents communication
Where this trial is running
Gebze, Kocaeli̇
- Kocaeli Üniversitesi — Gebze, Kocaeli̇, Turkey (Türkiye) (RECRUITING)
Study contacts
- Study coordinator: Gamze Reçber
- Email: gamzerecber147@gmail.com
- Phone: 905330921269
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.
Conditions: First Pregnancy