- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02648828
Understanding Physician Signout Risk Perception (UPS)
August 25, 2017 updated by: Janel Hanmer, University of Pittsburgh
The purpose of the study is to compare the ability of physicians and a statistical index (the Rothman score) to predict clinical deterioration over the next 24 hours.
Clinical deterioration is defined as concern in change in vital signs or patient status requiring a call to the rapid response team, cardiopulmonary arrest, or transfer to the ICU.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The proposed study will ask interns, residents, and attending physicians from general internal medicine teaching teams in a large teaching hospital to make predictions about the probability of their patient having a clinical deterioration in the next 24 hours.
The investigators will compare these judgments to the Rothman index.
Study Type
Observational
Enrollment (Actual)
132
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
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, United States, 15213
- University of Pittsburgh
-
-
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
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Cohorts will be selected from the teaching teams of the University of Pittsburgh's General Internal Medicine wards.
Description
Inclusion Criteria:
- Interns, residents, attendings in the Department of Medicine, Division of General Internal Medicine, University of Pittsburgh.
- Rotating on the general medical service at the University of Pittsburgh Medical Center - Presbyterian Hospital.
Exclusion Criteria:
- None
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Intern
Interns are in their first year of residency.
|
Patients at risk of clinical deterioration
|
Residents
Residents are in their 2nd or 3rd year of residency.
|
Patients at risk of clinical deterioration
|
Attendings
Attendings are physicians who have completed their residency.
|
Patients at risk of clinical deterioration
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Difference between physician prediction of risk of clinical deterioration and Rothman Index
Time Frame: Six months
|
Physicians will make judgments about the probability of clinical deterioration for each of their patients on a 0 (definitely won't) to 100 (certainly will) scale.
Clinical deterioration is defined as rapid response, cardiopulmonary arrest, or ICU transfer in the next 24 hours.
The Rothman Index is an index that predicts clinical deterioration.
The area under the receiver operating curve (AUROC) will be calculated for physicians and the Rothman Index.
The AUROC measures the association between the physician's judgment or Rothman Index and actual clinical deterioration.
The AUROC of these two measures will then be statistically compared.
|
Six months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Janel A Hanmer, M.D., University of Pittsburgh
- Principal Investigator: Alex Davis, PhD, Carnegie Mellon 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
July 1, 2015
Primary Completion (Actual)
February 1, 2016
Study Completion (Actual)
February 1, 2016
Study Registration Dates
First Submitted
July 20, 2015
First Submitted That Met QC Criteria
January 5, 2016
First Posted (Estimate)
January 7, 2016
Study Record Updates
Last Update Posted (Actual)
August 28, 2017
Last Update Submitted That Met QC Criteria
August 25, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- PRO15040582
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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