Actively Recruiting
Pushing Using Real-time Sonographic Ultrasound Education
Led by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Updated on 2025-08-22
136
Participants Needed
1
Research Sites
44 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study aims to assess whether the use of ultrasound during a pushing lesson can facilitate easier and safer childbirth. The research will be conducted at a single hospital and will involve pregnant women in their second trimester who enroll in an online childbirth course. Participants will be randomly assigned to one of two groups: One group will receive standard pushing instructions from a midwife. The other group will receive the same instructions along with a brief ultrasound session to visually support correct pushing techniques. The primary outcome is a potential reduction in the duration of the second stage of labor (when the baby is being delivered). Secondary outcomes include improved coordination of pelvic floor muscles, fewer perineal tears, a higher rate of vaginal births, reduced postnatal urinary incontinence, and greater maternal satisfaction. Approximately 136 women will be enrolled in the study (accounting for potential dropouts). The expectation is that this integrated teaching approach will enhance the effectiveness, safety, and overall experience of pushing during labor for both mothers and their newborns.
CONDITIONS
Official Title
Pushing Using Real-time Sonographic Ultrasound Education
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Nulliparous women in their second trimester (approximately 14-28 weeks of gestation)
- Willing to participate in a pushing techniques training program
- Singleton pregnancy
- Age 18 years or older
- Able to understand and provide informed consent in Italian
- Plan to deliver at Fondazione Policlinico Agostino Gemelli IRCCS
You will not qualify if you...
- Multifetal pregnancies (e.g., twins, triplets)
- Known obstetric complications or conditions preventing vaginal delivery (e.g., placenta previa)
- Medical or psychiatric conditions preventing participation or adherence
- History of pelvic floor surgery or severe pelvic floor dysfunction
- Unable to understand study requirements or provide informed consent
- Currently enrolled in conflicting clinical trials or interventions
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UOC Ostetricia e Patologia Ostetrica
Rome, RM, Italy, 00168
Actively Recruiting
Research Team
G
Gloria Anderson, PhD in Public Health
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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