Ultrasound Training Program for Gynecologic Cancer Staging in Residents

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorFondazione Policlinico Universitario Agostino Gemelli IRCCS

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

non-gynecology specialists, with attendance schedules at the center other than daily.

Failure to sign the informed consent by the participants.

Trial design

Design model

Single group

Treatments tested in this trial

  • Training Group

    Behavioral

    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.

Treatment groups

6 Participants
are divided into 1 treatment group
Group A: Training GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Agreement Rate Between Residents and Experts in Ultrasound-Based Staging of Gynecologic Cancers

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.

Time frame
Up to 6 months (from the start to the end of the training program)

Secondary outcomes

Other outcomes

Sponsors and contacts

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