Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
116 participants
INTERVENTIONAL
2016-10-31
2019-03-19
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
DOUBLE
Study Groups
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Control
Prompts standard to rounds or electronic medical records.
No interventions assigned to this group
Prompting Intervention
Prompting consideration of 3-month functional outcome.
Consideration of 3-month functional prognosis
Interventions
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Consideration of 3-month functional prognosis
Eligibility Criteria
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Inclusion Criteria
* At least 4 weeks of clinical work in an I.C.U. in the U.S.A. during the past 12 months
Exclusion Criteria
* Non-English speaking
* Primarily practicing medicine outside the U.S.A.
25 Years
ALL
No
Sponsors
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Gordon and Betty Moore Foundation
OTHER
Johns Hopkins University
OTHER
Responsible Party
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Principal Investigators
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Alison E Turnbull
Role: PRINCIPAL_INVESTIGATOR
Johns Hopkins University
Locations
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Johns Hopkins Hospital
Baltimore, Maryland, United States
Countries
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References
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Abshire MA, Li X, Basyal PS, Teply ML, Singh AL, Hayes MM, Turnbull AE. Actor feedback and rigorous monitoring: Essential quality assurance tools for testing behavioral interventions with simulation. PLoS One. 2020 May 29;15(5):e0233538. doi: 10.1371/journal.pone.0233538. eCollection 2020.
Turnbull AE, Hayes MM, Brower RG, Colantuoni E, Basyal PS, White DB, Curtis JR, Needham DM. Effect of Documenting Prognosis on the Information Provided to ICU Proxies: A Randomized Trial. Crit Care Med. 2019 Jun;47(6):757-764. doi: 10.1097/CCM.0000000000003731.
Other Identifiers
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IRB00082272
Identifier Type: -
Identifier Source: org_study_id
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