SW-RCT Implementation of Canadian Syncope Risk Score Based Practice Recommendations

ConditionSyncope
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorOttawa Hospital Research Institute

About this trial

Syncope is a common reason for emergency department (ED) presentation. While often benign, some patients have serious and life-threatening underlying causes, both cardiac and non-cardiac, which may or may not be apparent at the time of the initial ED assessment. Identifying which patients will benefit from further investigation, ongoing monitoring and/or hospital admission is essential to reduce both adverse outcomes and high costs. The research team has spent over a decade developing the evidence base for a risk stratification tool directed at optimizing the accuracy of ED decisions: the Canadian Syncope Risk Score (CSRS). This tool is now ready for the final phase of its introduction into clinical practice, namely a robust, multicentre implementation trial of the CSRS-based practice recommendations to demonstrate its real-world effectiveness. These recommendations, if applied, could lead to reduction in hospitalization with only 6% of high-risk patients requiring hospitalization, shorter ED lengths of stay for the 76% of ED syncope patients who are at low risk for 30-day serious outcomes, and more standardized disposition decisions, specifically discharge of 18% of medium-risk patients after appropriate discussion. Hence, the investigators hypothesize that an important reduction in hospitalization and ED disposition time can be achieved by implementing the CSRS-based recommendations with potential improvements in patient safety. The overall objective of this study is to evaluate the effectiveness of the knowledge translation (KT) of the CSRS-based practice recommendations in multiple Canadian EDs using a stepped wedge cluster randomized trial (SW-CRT) on health care efficiency and patient safety.

Eligibility criteria

Qualifiers

ED physicians involved in ED syncope care

Non-ED physicians involved in ED syncope care

Physician's delegates involved in ED syncope care

Disqualifiers

ED physicians not involved in ED syncope care

Non-ED physicians not involved in ED syncope care

Physician's delegates not involved in ED syncope care

Patients who are adults (aged > 18 years)

Trial design

Treatments tested in this trial

  • Knowledge translation (KT) of the CSRS based practice recommendations

Treatment groups

14,400 Participants
are divided into 1 treatment group

Locations

15
Foothills Medical Centre CalgaryAlberta, Canada
St. Boniface Hospital WinnipegManitoba, Canada
Health Sicence North Greater SudburyOntario, Canada
Hawkesbury and District General Hospital HawkesburyOntario, Canada

Sponsors and collaborators

Ottawa Hospital Research Institute

Lead sponsor