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Clinical Trials/NCT01150968
NCT01150968
Completed
N/A

An Educational Intervention to Improve Resident Comfort With Communication at the End of Life

University of California, San Francisco1 site in 1 country166 target enrollmentMarch 2010

Overview

Phase
N/A
Intervention
Not specified
Conditions
End of Life Communication
Sponsor
University of California, San Francisco
Enrollment
166
Locations
1
Primary Endpoint
Self-efficacy
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

The purpose of this study is to investigate whether the addition of teaching on communication at the end of life to the pre-existing resident curriculum will positively impact residents' knowledge and attitudes regarding communication at the end of life.

Detailed Description

Previous research has demonstrated a lack of resident training in communication at the end of life. This can lead to anxiety on the part of residents and poor experiences with these conversations. Residents at UCSF, and affiliated sites, participate in a daily formal teaching session from 12-1 pm and an informal case conference, known as Morning Report, from 7:30-8:30 am (8-9 am at VAMC). We propose to administer a pre-intervention survey to residents to assess knowledge and attitudes regarding communication at the end of life. Over two months, residents will receive one lecture during the noon session. Clinical cases will be presented for discussion during three sessions of morning report. All sessions are voluntary and take place at all three training sites, UCSF, SFGH, and the VAMC. As residents rotate every two months between the inpatient and outpatient settings, the intervention will be repeated once to ensure that the majority of residents have the opportunity to participate. A post-intervention survey, identical to the pre-intervention survey, will be administered to assess for impact of the educational intervention. This project only involves UCSF Internal Medicine residents. No patients will be involved in this study.

Registry
clinicaltrials.gov
Start Date
March 2010
End Date
June 2010
Last Updated
15 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • UCSF internal medicine resident

Exclusion Criteria

  • Not UCSF internal medicine resident

Outcomes

Primary Outcomes

Self-efficacy

Time Frame: 90 days

Residents participating in the intervention will demonstrate increased self-efficacy for end of life conversations.

Study Sites (1)

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