Assessing the Team SA Instrument in Measuring the Effectiveness of Communication Across Disciplines During ICU Rounds
Assessing the Utility of the Team SA Instrument in Measuring the Effectiveness of Communication Across Disciplines During ICU Rounds
1 other identifier
observational
240
1 country
1
Brief Summary
Assessing the utility of the Team SA instrument in measuring the effectiveness of communication across disciplines during ICU rounds.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2012
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2012
CompletedFirst Submitted
Initial submission to the registry
May 15, 2013
CompletedFirst Posted
Study publicly available on registry
May 17, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2013
CompletedSeptember 16, 2014
July 1, 2013
1 year
May 15, 2013
September 15, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
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.
Eligibility Criteria
Daily census rosters of the MICU and 8ICU nursing units will be reviewed for occupancy. At 8am on survey days occupied beds will be tallied (up to 39 beds). Beds occupied by a non-MICU service patient and those with active DNR-CC orders will be excluded. From the remaining patients, ten bed numbers will be randomly selected for review. Randomization will be stratified by MICU service sub-unit (MICU 40, MICU 90, 8ICU). If fewer than ten patients are eligible on an assigned survey day, all patients in the ICU on that day will be surveyed.
You may qualify if:
- 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.
You may not qualify if:
- N/A
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Naeem Ali, MDlead
Study Sites (1)
Davis Heart and Lung Research Institute 473 w. 12TH aVE
Columbus, Ohio, 43210, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Naeem Ali, MD
Ohio State University
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
May 15, 2013
First Posted
May 17, 2013
Study Start
July 1, 2012
Primary Completion
July 1, 2013
Study Completion
July 1, 2013
Last Updated
September 16, 2014
Record last verified: 2013-07