Recruiting

Observational Study

Sponsor:

University of Virginia

Code:

NCT04638530

Conditions

Resident Education, Patient Communication, Breaking Bad News to Patients Remotely, Telemedicine

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

Education on breaking bad news to family members remotely

Study Details

Brief summary:

Resident education on breaking bad news and conducting end of life conversations has been shown to improve comfort levels with having these conversations. Interventions with OB/GYN residents specifically have used a combination of didactics, resident role-playing and ultimately interaction with standardized patients with feedback from palliative care specialists. These interventions can be costly and also are not practical during the pandemic training environment where resident has transitioned to a virtual curriculum. While the didactics portions of this previously proven curriculum can be done virtually, the standardized patient interactions are challenging to replicate. Additionally, one of the key changes to patient care that has emerged during the pandemic is restrictive hospital and clinic visitor policies. Care providers must now have the ability to have difficult conversations and break bad news to family members over the phone rather than in person. Additionally, there has been an increasing reliance on telehealth visits. There are no currently studied training interventions in obstetrics and gynecology that address these skills.

Conditions

Resident Education, Patient Communication, Breaking Bad News to Patients Remotely, Telemedicine

Study ID

NCT04638530

Start date

Feb 1, 2021

Status verified date

Apr, 2021

Completion date

Jan 1, 2026

Anticipated

Primary completion date

Jan 1, 2025

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

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

Study Design

Enrollment

16 participants

Anticipated

Intervention Model

Single group

Primary purpose

Health Services Research

Interventions and Outcome Measures

Arms

other: Residents

All residents will participate in the activity

Interventions

Education on breaking bad news to family members remotely

Participants will receive a combination of surveys, pre- and post-tests, lectures and didactics to increase their awareness of techniques to communicate difficult topics with patients remotely as well as skill building exercises.

Primary outcome measure

  • Change in pre vs. post test scores [ Time Frame: 4 years ]

Central Contacts and Locations

Central contacts

Locations

University of Virginia

Recruiting

Charlottesville, Virginia, United States, 22908

Contacts

Principal Investigator:

Linda Duska, MD

More Information

Sponsor

University of Virginia

Last update posted

Apr 28, 2021

Last verified

Apr, 2021

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Virginia on 2021-04-28.