Actively Recruiting

All Genders
Healthy Volunteers
NCT05463536

Improvings: Implementing a Protocol to Improve Intrapartum Sonography Skills.

Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2024-07-03

20

Participants Needed

1

Research Sites

181 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Prospective observational cohort study on the learning curve for the sonographic assessment of labor progress (fetal head position and station) amongst obstetric caregivers. Study participants: convenience sample of 20 obstetric caregivers working in the department of obstetrics and gynecology at the University Hospital of Leuven - recruited over a 12-month period. Format of the training program: 1. Observational phase: the goal is to measure the accuracy of the clinical assessment of fetal head position and station throughout the different stages of labor by caregivers working within the department. 2. Self-study: reading of the 2018 practice guidelines on intra-partum ultrasound by ISUOG and watching the corresponding teaching video. 3. Supervised implementation phase: one-to-one teaching by experienced sonographers, who initially demonstrate, later interactively supervise the quality of the scans acquired by the obstetric caregiver. 4. Proficiency testing: from this point onwards, the trainee independently performs ultrasound scans in labor to asses fetal head position and station. The scans will be repeated by the expert sonographer, the results will be compared (qualitatively and quantitatively) and immediate feedback provided if indicated. Every observation will have a binary outcome (success or failure of trainee acquisition) according to predefined quality assessment criteria. Observations will be continued until proficiency is reached (saturation of the learning curve).

CONDITIONS

Official Title

Improvings: Implementing a Protocol to Improve Intrapartum Sonography Skills.

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Obstetric caregivers willing to participate in the study and provide written informed consent
Not Eligible

You will not qualify if you...

  • Trainees refusing to participate or not providing written informed consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

University Hospitals Leuven, department of obstetrics and gynaecology

Leuven, Belgium, 3000

Actively Recruiting

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Research Team

B

Bram Packet, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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