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N/A Completed N=109 Randomized Single-blind Other

Trial of Simulation-based Mastery Learning to Communicate Diagnostic Uncertainty

Uncertainty · Communication Research · Emergency Medicine
Source: ClinicalTrials.gov NCT04021771 ↗
Enrolled (actual)
109
Serious AEs
Results posted
May 2021
Primary outcomePrimary: % of Residents Who Pass the UCC at the T2 Assessment — 29; 2 Participants

Summary

The goal of this study is to teach emergency medicine resident physicians to communicate more effectively with patients at the time of emergency department discharge in the setting of diagnostic uncertainty (i.e. no definitive cause identified for the patient's symptoms). All residents will complete baseline and follow up assessments by completing in-person simulated patient discharged. After the baseline assessment, they will complete an online educational curriculum that has been developed by the study team, and will participate in video-based simulation deliberate practice (DP) and feedback sessions using a simulation-based mastery learning (SBML) approach. They will be assessed with the Uncertainty Communication Checklist (UCC), a tool already developed by the study team, that has a minimum passing standard (MPS) that was established through engagement of both patients and physicians. The investigators will perform a 2-arm wait-list randomized control trial with resident physicians to test the efficacy of the SBML curriculum in training residents to have a discharge discussion with patients discharged from the emergency department with diagnostic uncertainty.

Outcome Measures

OutcomeResultp-value
PRIMARY
% of Residents Who Pass the UCC at the T2 Assessment
29; 2
SECONDARY
Number of DP Sessions
1.7; 1.5; 1.0; 1.0; 2.4; 2.2
SECONDARY
Change in Pass Rates Within Groups From T2 to T3
29; 2; 30; 31

Eligibility Criteria

Inclusion Criteria

-Eligible participants include all emergency medicine residents at Thomas Jefferson University and Northwestern University.

Exclusion Criteria

-None

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04021771). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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