Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT07000240

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

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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

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

UOC Ostetricia e Patologia Ostetrica

Rome, RM, Italy, 00168

Actively Recruiting

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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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