We're building a better ClinicalTrials.gov. Check it out and tell us what you think!
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

What Influences Physicians' Decisions - Statistics or Stories?

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02048982
Recruitment Status : Withdrawn (Funding)
First Posted : January 29, 2014
Last Update Posted : September 12, 2018
Sponsor:
Collaborator:
Duke University
Information provided by (Responsible Party):
Weill Medical College of Cornell University

Brief 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.

Condition or disease Intervention/treatment Phase
Prescribing Tendencies Behavioral: Guideline Behavioral: Cost Behavioral: Victim Not Applicable

Detailed 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.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Health Services Research
Official Title: What Influences Physicians' Decisions - Statistics or Stories?
Study Start Date : February 2014
Actual Primary Completion Date : September 2015
Actual Study Completion Date : December 2015

Arm Intervention/treatment
Experimental: Guideline and Cost
The Choosing Wisely guideline and the cost of the test at our institution: $60.35 for a basic metabolic panel.
Behavioral: Guideline
Physicians will receive information on the Choosing Wisely Guideline

Behavioral: Cost
Physicians will receive cost information.

Placebo Comparator: Guideline
The Choosing Wisely guideline: "Don't perform blood chemistry panels in asymptomatic, healthy adults."
Behavioral: Guideline
Physicians will receive information on the Choosing Wisely Guideline

Active Comparator: Guideline and Victim
The Choosing Wisely Guideline and a clinical scenario with a patient as an identifiable victim who suffered harm from having an unnecessary test done
Behavioral: Guideline
Physicians will receive information on the Choosing Wisely Guideline

Behavioral: Victim
Physicians will receive information on an identifiable victim.

Experimental: Guideline, Cost, and Victim
The Choosing Wisely guideline and a clinical scenario with a physician as an identifiable victim who suffered harm when he ordered an unnecessary test.
Behavioral: Guideline
Physicians will receive information on the Choosing Wisely Guideline

Behavioral: Cost
Physicians will receive cost information.

Behavioral: Victim
Physicians will receive information on an identifiable victim.




Primary Outcome Measures :
  1. Percentage of blood chemistry tests among visits by adult patients under 65 [ Time Frame: Within 1 week of receiving the intervention ]
  2. Percentage of blood chemistry tests among visits by adult patients under 65 [ Time Frame: Within 1 month of receiving the scenario ]

Secondary Outcome Measures :
  1. Physicians' attitudes and perceived practice immediately after reading the scenario [ Time Frame: Immediate (up to 5 min) ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Primary care physicians in the Weill Cornell Physicians Organization

Exclusion Criteria:

  • None

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02048982


Locations
Layout table for location information
United States, New York
Weill Cornell Medical College
New York, New York, United States, 10065
Sponsors and Collaborators
Weill Medical College of Cornell University
Duke University
Layout table for additonal information
Responsible Party: Weill Medical College of Cornell University
ClinicalTrials.gov Identifier: NCT02048982    
Other Study ID Numbers: Bishop_stats_stories
First Posted: January 29, 2014    Key Record Dates
Last Update Posted: September 12, 2018
Last Verified: September 2018
Keywords provided by Weill Medical College of Cornell University:
physician prescribing
behavioral economics
primary care practice