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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02048982
Other study ID # Bishop_stats_stories
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date February 2014
Est. completion date December 2015

Study information

Verified date September 2018
Source Weill Medical College of Cornell University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to test whether physicians change their use of non-recommended tests, procedures, or medications more in response to evidence based-guidelines, price information, or an individual patient's story.


Description:

We will perform a randomized controlled trial (RCT) of information presented to physicians to test the hypothesis that an identifiable victim affects physician practice behavior more than a statistical victim.

Specifically, we will answer the following research questions: 1) do physicians order fewer non-recommended tests, procedures, or medications if they are told about a patient or a physician who had a bad outcome from that test, procedure, or medication than if they are simply told the guideline or the cost of the test, procedure or medication, 2) does the effect of learning about the identifiable victim last longer than the effect of learning about the guideline or the cost of a test, procedure, or medication, and 3) does the identifiable victim effect differ if the victim is a patient or a physician? We hypothesize that because of the propensity to respond more to the identifiable victim rather than the statistical victim that physicians will order fewer unnecessary tests when they are told about an individual patient case than if they are simply told about the guideline, that the effect of the identifiable victim will last longer than the effect of the statistical victim, and that a patient as the identifiable victim will have more effect than a physician as the identifiable victim.

The identifiable victim effect refers to the tendency to offer more aid to a specific, identifiable victim rather than a vaguely defined group of people with the same need. In the this study, the identifiable victim is a fictional patient who experience a negative consequence as a result of an unnecessary test. The identifiable victim effect is described and studied in the following articles:

Small D. Sympathy and callousness: The impact of deliberative thought on donations to identifiable and statistical victims. Organizational Behavior and Human Decision Processes 2007;102:143-53.

George Loewenstein, Deborah A. Small, and Jeff Strand. "Statistical, identifiable, and iconic victims" in Edward J. McCaffery, Joel Slemrod (2006). Behavioral public finance. Russell Sage Foundation; pp. 32-35.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2015
Est. primary completion date September 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Primary care physicians in the Weill Cornell Physicians Organization

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Guideline
Physicians will receive information on the Choosing Wisely Guideline
Cost
Physicians will receive cost information.
Victim
Physicians will receive information on an identifiable victim.

Locations

Country Name City State
United States Weill Cornell Medical College New York New York

Sponsors (2)

Lead Sponsor Collaborator
Weill Medical College of Cornell University Duke University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of blood chemistry tests among visits by adult patients under 65 Within 1 week of receiving the intervention
Primary Percentage of blood chemistry tests among visits by adult patients under 65 Within 1 month of receiving the scenario
Secondary Physicians' attitudes and perceived practice immediately after reading the scenario Immediate (up to 5 min)