Enhanced Critical Care Air Transport Team Training for Mitigation of Task Saturation

This study has been completed.
Sponsor:
Collaborator:
United States Air Force
Information provided by (Responsible Party):
University of Cincinnati
ClinicalTrials.gov Identifier:
NCT01628224
First received: November 18, 2011
Last updated: March 4, 2013
Last verified: March 2013
  Purpose

This study involves two tasks. The first involves observation of patient care during simulated aeroevacuation missions in order to gauge task saturation. The second involves review of records from actual evacuation flights in order to determine the effects of task saturation on patient care.


Condition
Task Saturation

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Enhanced Critical Care Air Transport Team Training for Mitigation of Task Saturation

Resource links provided by NLM:


Further study details as provided by University of Cincinnati:

Primary Outcome Measures:
  • Incidence of task saturation [ Time Frame: 1 hour ] [ Designated as safety issue: Yes ]
    Task saturation is defined as the point at which the volume or complexity of events exceeds the capability of the individual or team to maintain a standard of care.


Enrollment: 48
Study Start Date: October 2011
Study Completion Date: January 2013
Primary Completion Date: February 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts
CCATT Team
Measurements will be taken on groups of 3 people each. There will be a total of 16 such teams, with total membership of 48 individuals

  Eligibility

Ages Eligible for Study:   18 Years to 60 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

The population for the first task will consist of 4 CCATT teams (of 3 members each)

Criteria

Inclusion Criteria:

  • Enrollment in a US Air Force CCATT Advanced Class at University Hospital, Cincinnati
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01628224

Locations
United States, Ohio
University Hospital
Cincinnati, Ohio, United States, 45219
Sponsors and Collaborators
University of Cincinnati
United States Air Force
Investigators
Principal Investigator: Tim Pritts, MD University of Cincinnati
  More Information

No publications provided

Responsible Party: University of Cincinnati
ClinicalTrials.gov Identifier: NCT01628224     History of Changes
Other Study ID Numbers: Pritts-2010-01
Study First Received: November 18, 2011
Last Updated: March 4, 2013
Health Authority: United States: Institutional Review Board

Keywords provided by University of Cincinnati:
Task saturation

ClinicalTrials.gov processed this record on July 22, 2014