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Ultrasound Training Program for Gynecologic Cancer Staging in Residents

Development and Validation of an Ultrasound Training Program for Residents in Staging Gynecological Cancers (Ovarian Cancer, Endometrial Cancer and Cervical Cancer)

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07028229
Acronym
Ultra-teaching
Enrollment
6
Registered
2025-06-19
Start date
2025-06-16
Completion date
2025-12-30
Last updated
2025-06-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervix Cancer, Endometrial Cancer, Medical Education, Ovarian Cancer

Keywords

Resident Training, Learning Curve, Gynecologic Oncology, Transvaginal Ultrasound

Brief summary

This is a prospective, interventional study aiming to develop and validate an ultrasound training program for gynecology and obstetrics residents, focused on the staging of gynecologic cancers, including ovarian, endometrial, and cervical cancer. The program consists of theoretical lectures, practical hands-on sessions, and supervised clinical case evaluations over a six-month period. Residents will perform ultrasound examinations independently, which will be compared to those conducted by expert sonographers. The primary objective is to assess the learning curve of each trainee by evaluating diagnostic concordance with expert findings across specific staging parameters.

Interventions

BEHAVIORALTraining Group

A structured educational and practical training program in gynecologic oncology ultrasound designed for residents. The intervention includes lectures, clinical case discussions, supervised and independent ultrasound examinations, and performance assessments to evaluate learning progression and diagnostic concordance with experts.

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* At least six gynecology residents who will regularly attend the ultrasound center daily, with overlapping shifts. * All patients with a diagnosis or suspected diagnosis of gynecological cancer, including ovarian, endometrial, and cervical cancers, will be included in the study and scanned by both residents and experts. * Signing of the informed consent by the participants.

Exclusion criteria

* non-gynecology specialists, with attendance schedules at the center other than daily. * Failure to sign the informed consent by the participants.

Design outcomes

Primary

MeasureTime frameDescription
Agreement Rate Between Residents and Experts in Ultrasound-Based Staging of Gynecologic CancersUp to 6 months (from the start to the end of the training program)Assessment of the diagnostic concordance between ultrasound staging performed by residents and expert sonographers, measured across defined anatomical and pathological parameters (e.g., lymph node involvement, carcinomatosis, tumor size and spread). Concordance will be quantified as the percentage of agreement per case and per parameter.

Countries

Italy

Contacts

Primary ContactAntonia Carla Testa
antoniacarla.testa@policlinicogemelli.it0630156399
Backup ContactFrancesca Moro
francesca.moro@guest.policlinicogemelli.it0630156399

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026