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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00859066
Other study ID # HUM00026874
Secondary ID
Status Terminated
Phase N/A
First received March 9, 2009
Last updated April 26, 2012
Start date January 2009
Est. completion date December 2011

Study information

Verified date April 2012
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to quantify levels of resident anxiety under the current system (take call alone) and compare results to a modified system.


Description:

The study purpose is to quantify resident perceptions and feelings under the current 1700 call system (take call alone) and compare those with resident perceptions and feelings under a modified system where two partial shifts are taken with an experienced resident ("buddy call") prior to taking call alone.


Recruitment information / eligibility

Status Terminated
Enrollment 19
Est. completion date December 2011
Est. primary completion date October 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- first year radiology residents

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Michigan Hospital Ann Arbor Michigan

Sponsors (1)

Lead Sponsor Collaborator
University of Michigan

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improve resident well-being by decreasing anxiety surrounding beginning ER call as a first year radiology resident. 12 months No
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