The Impact of Emergency Physician Empathy on Litigation Propensity

October 1, 2014 updated by: Dustin Smith, Loma Linda University
The purpose of this study is to observe whether people would report being less likely to sue a physician who shows more empathy when giving a patient potentially bad news regarding their medical condition.

Study Overview

Status

Completed

Conditions

Detailed Description

The investigators hypothesized that patients will have less propensity to sue emergency physicians after a poor outcome if the physician demonstrated empathy by verbalizing that they recognize the patient is concerned about their symptoms, and that the patient knows their typical state of health better than a physician seeing them for the first time. Accordingly, the investigators will assess whether the presence or absence of emergency physician empathetic statements in videotaped simulated encounters will alter patient propensity towards litigation. Secondary objectives are to assess whether the presence or absence of empathetic statements alters patient perceptions of discharge instruction clarity, physician expertness, physician caring, and physician desirability.

Study Type

Observational

Enrollment (Actual)

437

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Loma Linda, California, United States, 92354
        • Loma Linda University Emergency Department

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Emergency room patients

Description

Inclusion Criteria:

  • Emergency Room Patient

Exclusion Criteria:

  • Non-English speaking
  • Not healthy enough to be in waiting room

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Emergency Room Patients

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intention to sue
Time Frame: Immediately after viewing
This outcome will be assessed by asking "Would you sue this doctor?" after viewing a short video. Items will be measured on a 5-point scale (1=Definitely no to 5=Definitely yes).
Immediately after viewing

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessment of physician expertise
Time Frame: Immediately after viewing
This outcome will be assessed by asking "Do you believe this physician is an expert?" after viewing a short video. Items will be measured on a 5-point scale (1=Definitely no to 5=Definitely yes).
Immediately after viewing
Assessment of physician caring
Time Frame: Immediately after viewing
This outcome will be assessed by asking "Do you think this doctor cared about the patient?" after viewing a short video. Items will be measured on a 5-point scale (1=Definitely no to 5=Definitely yes).
Immediately after viewing
Assessment of whether subject would want to be physician's patient
Time Frame: Immediately after viewing
This outcome will be assessed by asking "Would you want this physician as your doctor?" after viewing a short video. Items will be measured on a 5-point scale (1=Definitely no to 5=Definitely yes).
Immediately after viewing
Assessment of clarity of physician instructions
Time Frame: Immediatley after viewing
This outcome will be assessed by asking "Did you understand the instructions the doctor gave the patient?" after viewing a short video. Items will be measured on a 5-point scale (1=Definitely no to 5=Definitely yes).
Immediatley after viewing

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Dustin Smith, MD, Loma Linda University
  • Study Director: Ellen Reibling, PhD, Loma Linda University
  • Study Director: Jesse Kellar, MD, Loma Linda University
  • Study Director: Steve Green, MD, Loma Linda University
  • Study Director: Elizabeth Walters, MD, Loma Linda University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2013

Primary Completion (Actual)

June 1, 2013

Study Completion (Actual)

December 1, 2013

Study Registration Dates

First Submitted

April 18, 2013

First Submitted That Met QC Criteria

April 22, 2013

First Posted (Estimate)

April 23, 2013

Study Record Updates

Last Update Posted (Estimate)

October 3, 2014

Last Update Submitted That Met QC Criteria

October 1, 2014

Last Verified

October 1, 2014

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • RS-5120206

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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