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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01856608
Other study ID # 2012B0233
Secondary ID
Status Completed
Phase N/A
First received May 15, 2013
Last updated September 15, 2014
Start date July 2012
Est. completion date July 2013

Study information

Verified date July 2013
Source Ohio State University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Assessing the utility of the Team SA instrument in measuring the effectiveness of communication across disciplines during ICU rounds.


Description:

Multidisciplinary rounds are events that occur daily in Intensive care units. During these events, practitioners from multiple disciplines meet at a pre-specified time to discuss current medical condition and plans of care. At the conclusion of these discussions, all practitioners are expected to understand the plan of care well enough to execute defined tasks, but also coordinate as circumstances change. In order to coordinate under changing circumstances practitioners must have a broader understanding of the current state of the patient and how likely certain deteriorations are. This synthetic understanding of patient risks across multi-provider groups has been described as anticipatory team situational awareness (Team SA). One instrument has been validated in the ICU as feasible and informative. This Team SA survey successfully identified that the time spent in "training" discussions improved Team SA across physician groups. The investigators' goal is to implement this survey across the investigators' medical ICU service to obtain a baseline estimate of how effective current communication patterns are for achieving concordant Team SA. If gaps in communication are encountered future interventions will be developed


Recruitment information / eligibility

Status Completed
Enrollment 240
Est. completion date July 2013
Est. primary completion date July 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 17 Years to 70 Years
Eligibility Inclusion Criteria:

- Nurses, primary clinicians (resident or NP) and Critical Care physicians (Staff or Fellow in Critical Care Medicine) will be approached for interview. All subjects will be approached individually and asked to participate outside of the presence of the other potential study subjects.

Exclusion Criteria:

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Davis Heart and Lung Research Institute 473 w. 12TH aVE Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Naeem Ali, MD

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To determine if it is feasible to survey clinicians regarding their opinions about future risks for individual patients in the ICU setting To determine the range of team situational awareness exhibited by current ICU clinician teams It is expected that a maximum of ten minutes will be required to complete the survey. No
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