Improving ultrasound skills for labor assessment among obstetric caregivers
Improvings: Implementing a Protocol to Improve Intrapartum Sonography Skills.
This study is testing whether training obstetric caregivers to use ultrasound can help them better assess fetal head position during labor.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 20 (estimated) |
| Sex | All |
| Sponsor | Universitaire Ziekenhuizen KU Leuven Academic / other |
| Locations | 1 site (Leuven) |
| Trial ID | NCT05463536 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the learning curve of obstetric caregivers in accurately assessing fetal head position and station during labor using ultrasound. It involves a convenience sample of 20 caregivers from the University Hospital of Leuven, who will undergo a structured training program consisting of observational assessments, self-study of guidelines, and supervised practice. The study will measure the accuracy of clinical assessments throughout different stages of labor, with experienced sonographers verifying the findings. The goal is to enhance the skills of caregivers in using ultrasound for better labor management.
Who should consider this trial
Good fit: Ideal candidates for this study are obstetric caregivers willing to participate and improve their ultrasound skills.
Not a fit: Patients who are not involved in the training or assessment process may not receive direct benefits from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved accuracy in labor assessments, enhancing maternal and fetal outcomes.
How similar studies have performed: While the specific approach of this study may be novel, similar studies have shown that training in ultrasound can improve clinical assessment skills in obstetric care.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Obstetric caregivers, willing to participate in the study (to give written informed consent). Exclusion Criteria: * Trainees refusing to participate (refusing to give written informed consent).
Where this trial is running
Leuven
- University Hospitals Leuven, department of obstetrics and gynaecology — Leuven, Belgium (Recruiting)
Study contacts
- Principal investigator: Jute Richter, MD, PhD — UZ Leuven / KU Leuven
- Study coordinator: Bram Packet, MD
- Email: bram.packet@kuleuven.be
- Phone: 00321648824
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.