CompletedNot Applicable

Deimplementing CXR After CVC (DRAUP) in the ICU

United States101 participantsStarted 2024-01-01

Plain-language summary

This study proposes adapting and testing an innovative, behavioral theory-driven deimplementation program called DRAUP in two intensive care units for proof of concept and support that the program can help providers and hospital organizations address context determinants of deimplementation. Study data will be used to optimize the intervention for a subsequent larger trials.

Who can participate

Age range18 Years

SexALL

See this in plain English?

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-Measure the effectiveness and cost effectiveness of DRAUP on discontinuation of CXRs Inclusion Criteria for DRAUP training: (1) ICU faculty, fellows, senior residents (post graduate year 3) and advanced practice practitioners * ICU inclusion for DRAUP program: * Availability of ultrasound machines with archiving capability (DICOM) * A minimum of 100 supradiaphragmatic CVC insertions annually in adult patients (age \>18) * Capacity to access digital archiving (PICOM) * Patient inclusion for DRAUP program: * supradiaphragmatic CVC placed * Patient exclusion for DRAUP program: * severe instability (cardiac arrest, severe shock) where CVC would be used without CXR, * level 1 trauma; * burn patients with no viable skin surface for imaging

What they're measuring

DRAUP in

Timeframe: 24 months

Trial details

NCT IDNCT06146348

SponsorWashington University School of Medicine

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-12-31

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