2022
DOI: 10.1186/s40814-022-01212-y
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Testing the feasibility, acceptability, and preliminary effect of a novel deliberate practice intervention to reduce diagnostic error in trauma triage: a study protocol for a randomized pilot trial

Abstract: Background Non-compliance with clinical practice guidelines in trauma remains common, in part because physicians make diagnostic errors when triaging injured patients. Deliberate practice, purposeful participation in a training task under the oversight of a coach, effectively changes behavior in procedural domains of medicine but has rarely been used to improve diagnostic skill. We plan a pilot parallel randomized trial to test the feasibility, acceptability, and preliminary effect of a novel d… Show more

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(2 citation statements)
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“…We structured the process evaluation of the intervention using the Proctor framework of outcomes for implementation research and followed the Consolidated Standards of Reporting Trials Extension (CONSORT Extension) reporting guideline (ie, extension for pilot and feasibility trials) in reporting our results . We previously published the trial protocol with a priori hypotheses about criteria for defining success . The University of Pittsburgh Human Research Protection Office approved the study.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…We structured the process evaluation of the intervention using the Proctor framework of outcomes for implementation research and followed the Consolidated Standards of Reporting Trials Extension (CONSORT Extension) reporting guideline (ie, extension for pilot and feasibility trials) in reporting our results . We previously published the trial protocol with a priori hypotheses about criteria for defining success . The University of Pittsburgh Human Research Protection Office approved the study.…”
Section: Methodsmentioning
confidence: 99%
“… 20 , 21 We previously published the trial protocol with a priori hypotheses about criteria for defining success. 22 The University of Pittsburgh Human Research Protection Office approved the study. Trial participants provided digital written informed consent at the time of enrollment (trial protocol in Supplement 1 ).…”
Section: Methodsmentioning
confidence: 99%