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| Sponsors and Collaborators: |
University of Zurich Swiss Federal Institute of Technology |
|---|---|
| Information provided by: | University of Zurich |
| ClinicalTrials.gov Identifier: | NCT00706108 |
Purpose
The impact of different coordination patterns on team performance during anesthesia inductions are analyzed using videotapes. These records are examined using various categorization systems (ETHZ), focussing on changes of coordinative behaviour with shifting situational requirements. A multicategorial rating system is used to evaluate team performance. An integrated simulator study facilitates validation of the rating system.
| Condition | Intervention |
|---|---|
|
Anesthesia Team Coordination |
Behavioral: Observational study |
| Study Type: | Observational |
| Official Title: | Adaptive Coordination in Anaesthesia Teams and Its Relationship to Clinical Performance. (Cooperative Project ETHZ, OAT, Prof. G. Grote, and IfA/USZ; Founding by Swiss National Science Foundation to Both Institutions) |
| Estimated Enrollment: | 550 |
| Study Start Date: | January 2005 |
| Estimated Study Completion Date: | December 2009 |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
1
Simulation of anesthesia induction with critical incidents: Analysis of technical and non-technical performance (15 Teams)
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2
Analysis of technical and non-technical performance in live anesthesia inductions (40 teams)
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3
Simulation of anesthesia inductions with advanced simulated critical incidents or events and analysis of technical and non-technical performance (max. 50 teams) |
Behavioral: Observational study
Observational (descriptive) study of technical and non-technical performance
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Video tapes and vital parameter readings are recorded with a setup allowing synchronized recordings. Thus, exact timing between events on different data channels can be determined. Data are analyzed for unforeseen events, technical performance, and team coordination / non-technical performance.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Anesthesia personnel (nurse anesthetists, anesthesia residents, staff anesthetists, OR attendants, other members of anesthesia / perioperative team)and patients as seen on video; all if informed consent was obtained
Inclusion criteria:
Exclusion criteria:
Contacts and Locations| Contact: Johannes Wacker, MD | +41 (0)44 255 11 11 | johannes.wacker@usz.ch |
| Switzerland | |
| Institute of Anesthesiology, University Hospital Zurich | Recruiting |
| Zurich, Switzerland, CH-8091 | |
| Contact: Johannes Wacker, MD +4144 2555987 johannes.wacker@usz.ch | |
| Principal Investigator: Johannes Wacker, MD | |
| Study Director: | 01 Studienregister MasterAdmins | UniversitaetsSpital Zuerich |
| Study Director: | Donat R. Spahn, Prof., MD | Institute of Anesthesiology, University Hospital Zurich |
| Principal Investigator: | Johannes Wacker, MD | Institute of Anesthesiology, University Hospital Zurich |
| Study Chair: | Gudela Grote, Prof., PhD | Swiss Federal Institute of Technology ETH Zurich, OAT |
More Information
| Responsible Party: | University Hospital Zurich ( Johannes Wacker, Institute of Anesthesiology, University Hospital Zurich ) |
| Study ID Numbers: | SNF 100013-116673 / |
| Study First Received: | June 25, 2008 |
| Last Updated: | June 26, 2008 |
| ClinicalTrials.gov Identifier: | NCT00706108 History of Changes |
| Health Authority: | Switzerland: Ethikkommission |
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Anesthetics |
