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Task SaturationNCT01628224

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

An observational study of Task Saturation, run by University of Cincinnati at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Task Saturation
How many people
48 participants
Where
1 siteUnited States
Study dates
Oct 2011to Jan 2013
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

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

Who may be able to join

  • Enrollment in a US Air Force CCATT Advanced Class at University Hospital, Cincinnati

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University Hospital

    Cincinnati, Ohio, 45219

Other trials in United States

About this study

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.

Conditions
Task Saturation
Keywords
Task saturation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01628224
Study groupRoleWhat they receive
CCATT TeamMeasurements will be taken on groups of 3 people each. There will be a total of 16 such teams, with total membership of 48 individuals

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Incidence of task saturation

    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.

    Measured: 1 hour

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jun 2012 (estimated)
  2. Study startOct 2011
  3. Primary completionFeb 2012
  4. Study completionJan 2013

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
48 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01628224
Sponsor's protocol ID
Pritts-2010-01
Status last verified
Mar 2013
First submitted
18 Nov 2011
Last updated
5 Mar 2013
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Task Saturation, run by University of Cincinnati at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Mar 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Incidence of task saturation (time frame: 1 hour). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Mar 2013.

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