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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01859286
Other study ID # HSC-MS-11-0655
Secondary ID
Status Completed
Phase N/A
First received April 27, 2013
Last updated May 17, 2013
Start date February 2012

Study information

Verified date May 2013
Source The University of Texas Health Science Center, Houston
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The investigators sought to determine if implementing a standardized sign out process would reduce the amount of medical errors related to patient sign out. The standardized process included the following interventions: implementation of a data resident to review patients lab values, vital signs, radiologist results, and orders in real time, conducting sign out in a standardized location and using the attending physician as an "interruption manager." The investigators defined medical errors related to sign out as any piece of information was incorrectly reported or omitted during sign out that caused a change in treatment or disposition discussed during sign out. The investigators hypothesis was that implementing a standardized sign out process would lead to a decrease in the amount of sign out related errors.


Recruitment information / eligibility

Status Completed
Enrollment 321
Est. completion date
Est. primary completion date May 2012
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- ED transfers of care occurring at 0700 or 1900.

Exclusion Criteria:

- Attending only handovers (1500, 2300)

- Handovers including midlevel providers (Thursday 0700, 1300).

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Emergencies
  • Medical Errors Related to Emergency Department Sign Out

Intervention

Other:
standardized sign out process
The intervention phase included was the introduction of a standardized TOC (transfer of care) process, which occurred during April and May of 2012. TOC was done at a predefined location in each section of the emergency department (Medicine and Trauma). All participating residents were given a diagram detailing the central location and seating arrangement. The outgoing attending was designated to handle all distractions or disturbances that occurred during sign out. The most senior resident coming on to shift was designated the data resident. The data resident's role was to operate a centralized computer with the ED tracking board and EMR and review pending orders, vital signs and resulted labs and radiology reports after each patient was signed out. A brief pause was implemented to allow the oncoming team to ask any questions regarding that patient's care or course. The post TOC data form and protocol were identical to that of the control phase.

Locations

Country Name City State
United States Memorial Hermann Hospital - Texas Medical Center Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
The University of Texas Health Science Center, Houston

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sign out related errors 4 months Yes
Secondary perception of sign out 1 year after implementation of revised sign out process Yes