Training OB/GYN residents to communicate bad news to families during a pandemic
Breaking Bad News to Family Members in a Pandemic
This study is trying to help OB/GYN residents learn how to communicate difficult news to families during the pandemic, even when they can't meet in person.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 16 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Virginia Academic / other |
| Locations | 1 site (Charlottesville, Virginia) |
| Trial ID | NCT04638530 on ClinicalTrials.gov |
What this trial studies
This study focuses on enhancing the communication skills of OB/GYN residents in breaking bad news to family members, particularly in a remote setting due to pandemic restrictions. It involves a combination of didactic sessions, role-playing, and discussions led by experienced faculty members. Residents will complete a pre-study questionnaire to assess their prior experiences and comfort levels with end-of-life conversations. The goal is to equip residents with the necessary skills to handle difficult conversations effectively, even when in-person interactions are not possible.
Who should consider this trial
Good fit: Ideal candidates for this study are residents enrolled in the University of Virginia's residency program in Obstetrics and Gynecology.
Not a fit: Patients who are not part of the University of Virginia's residency program or those under 18 years old will not benefit from this study.
Why it matters
Potential benefit: If successful, this training could significantly improve the ability of residents to communicate effectively with families during critical moments, enhancing patient care.
How similar studies have performed: While similar educational interventions have shown success in improving communication skills, this specific approach during a pandemic is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * residents in University of Virginia's residency in Obstetrics and Gynecology * able to provide informed consent Exclusion Criteria: * under age 18 * inability to give informed consent
Where this trial is running
Charlottesville, Virginia
- University of Virginia — Charlottesville, Virginia, United States (Recruiting)
Study contacts
- Study coordinator: Rache l M Lacy, MPH
- Email: rmc9p@hscmail.mcc.virginia.edu
- Phone: 434-243-0126
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.