- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01837706
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
-
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California
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Loma Linda, California, United States, 92354
- Loma Linda University Emergency Department
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-
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 |
|---|
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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.
Sponsor
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
Keywords
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.