Using a home ultrasound device for visual biofeedback before labor
Prelabor Maternal Pushing Training Using Visual Biofeedback by a Self-operated Ultrasound Device
This study is testing whether using a home ultrasound device to practice pushing techniques can help expectant mothers feel more confident and satisfied during labor.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 261 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Rabin Medical Center Academic / other |
| Locations | 1 site (Petah Tikva) |
| Trial ID | NCT06049784 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of visual biofeedback prior to labor through a self-operated home ultrasound device aimed at training mothers on pushing techniques. Participants will attend a single training session at the hospital, followed by a two-week home intervention. The study will assess the impact of this training on obstetric and psychological outcomes, including the duration of labor, maternal confidence, and overall satisfaction with the birthing experience. Data will be collected through medical records and self-report questionnaires before and after childbirth.
Who should consider this trial
Good fit: Ideal candidates for this study are nulliparous women with singleton pregnancies who are planning for a vaginal delivery and have low-risk pregnancies.
Not a fit: Patients with multifetal gestation or contraindications for vaginal delivery, as well as those with high-risk pregnancies, may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce fear of childbirth and improve maternal and neonatal outcomes during labor.
How similar studies have performed: Previous studies have shown success with in-hospital visual biofeedback during labor, but this approach using a home ultrasound device is novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Nuliparity * Singleton pregnancy * Planned for vaginal delivery * Low risk pregnancy * Ability to fulfill a questionnaire Exclusion Criteria: * Multifetal gestation * Contraindications for vaginal delivery (Placenta previa, Breech presentation etc.) * High risk pregnancy
Where this trial is running
Petah Tikva
- Rabin Medical Center — Petah Tikva, Israel (Recruiting)
Study contacts
- Principal investigator: Sharon Perlman, MD — Rabin Medical Center, affiliated to the Tel Aviv University, Tel Aviv, Israel
- Study coordinator: Shira Waks
- Email: Shiraw@clalit.org.il
- Phone: 972528557212
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.