About this trial
The purpose of this trial is to evaluate if augmenting a usual audit and feedback implementation approach with telehealth-enabled support improves coordinated spontaneous awakening/breathing trials and patient outcomes for mechanically ventilated patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patient age >=16 years admitted to study hospital ICU
Intubated and mechanically ventilated
Disqualifiers
Patient with pre-existing brain death admitted to study hospital for organ donation
Died within 24 hours of intubation
Trial design
Parallel
Treatments tested in this trial
Telehealth- enabled support for SAT/SBT adherence
Other interventionTelehealth-enabled support over and above usual audit and feedback includes identifying candidates for spontaneous awakening and breathing trials, prompting bedside providers and guiding execution of the coordinated spontaneous awakening and breathing trials as needed.
Usual audit and feedback for SAT/SBT adherence
Other interventionUsual audit and feedback
Treatment groups
Trial outcomes
Primary outcomes
Adherence to C-SAT/SBT
Fraction of eligible days on which coordinated spontaneous awakening trial and spontaneous breathing trial completed.
Ventilator-free days to day 28
ventilator-free days to day 28
Secondary outcomes
30-day Mortality
Hospital Length of Stay
90-day Mortality
New ventilator-associated pneumonia
Sponsors and contacts
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Intermountain Health Care, Inc.
Lead sponsor
University of Utah
Collaborator
National Heart, Lung, and Blood Institute (NHLBI)
Collaborator