The Fundamentals of Communication in Surgery

NCT06654310 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2025-09-30

No results posted yet for this study

Summary

The goal of this observational study is to evaluate the impact of the FCS curriculum on achieving the learning objectives and resident reported self-efficacy with communication skills and determine the scalability of the training across a range of general surgery training programs

Conditions

  • Communication Research
  • Communication Programs

Interventions

BEHAVIORAL

Delivery of FCS Skills Curriculum

The UW study team will conduct two 2-hour train-the-trainer sessions with all surgical attendings who have committed to participation as a trainer in the FCS curriculum. The designated trainer will deliver each 2-hour session during the existing formal educational time for residents. If existing protected educational time will not allow for a 2-hour training session, the sessions can be delivered in two 1-hour sessions. These sessions will be incorporated into the curriculum similar to all other formal training provided to residents with the same expectations to attend. Each 2-hour FCS session starts with a 30-minute exercise in empathic communication. The remaining 90 minutes are devoted to skills that support decision making about surgery.

Sponsors & Collaborators

  • Josiah Macy, Jr. Foundation

    collaborator UNKNOWN
  • University of Oklahoma

    collaborator OTHER
  • University of Pittsburgh

    collaborator OTHER
  • University of South Florida

    collaborator OTHER
  • West Virginia University

    collaborator OTHER
  • Duke University

    collaborator OTHER
  • Association for Academic Surgery

    collaborator UNKNOWN
  • Inova Fairfax Medical Campus

    collaborator UNKNOWN
  • University of Wisconsin, Madison

    lead OTHER

Principal Investigators

  • Margaret (Gretchen) L Schwarze, MD, MPP · University of Wisconsin, Madison

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-09-16
Primary Completion
2027-05-01
Completion
2027-07-01

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06654310 on ClinicalTrials.gov