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Clinical Trials in Canada / NCT05900414
Recruiting Not applicable

RAPID AFib Decision Aid for Stroke Prevention in Atrial Fibrillation

NCT05900414 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2024-04-01
Last updated
2025-04-02

Condition(s) studied

Atrial Fibrillation

Investigational drug(s) / intervention(s)

Electronic patient decision aidInformation

Electronic patient decision aid: Link to website with information about atrial fibrillation treatments, plus access to the web-based patient decision aid to enable shared decision making between patients and their physicians for atrial fibrillation stroke prevention treatments

Information: Link to website with information about atrial fibrillation treatments

Study summary

The goal of this pilot clinical trial is to evaluate the utility of a new electronic patient decision aid for stroke prevention therapy in patients with atrial fibrillation. The main questions it aims to answer are:

Is the patient decision aid acceptable to both patients and physicians? Does the patient decision aid lead to more effective shared decision-making than standard care among patients with atrial fibrillation who are considering stroke prevention therapy? Participants with a recent diagnosis of atrial fibrillation will be enrolled before an upcoming specialist physician visit. Researchers will compare a pre-visit intervention consisting of standard educational materials plus use of the patient decision aid to educational materials alone to see if using the decision aid results in improved shared decision making during the clinic visit.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Non-valvular AF diagnosed within 12 months, with any level of stroke risk assessed by CHA2DS2-VASc score. * Age 18 or older * Either no OAC treatment or treated for less than 90 days. * Initial specialist AF visit scheduled in 7-30 days. Exclusion Criteria: * Valvular AF, defined, per Canadian Cardiovascular Society Guidelines, as AF in the presence of mechanical heart valves, rheumatic mitral stenosis, or moderate to severe nonrheumatic mitral stenosis. * Currently prescribed dual antiplatelet therapy (ASA plus either clopidogrel, ticagrelor, or prasugrel) for an indication other than AF. * Has an independent, non-AF indication for oral anticoagulation. * Has a non-modifiable impediment to effective use of web-based tools. Examples include lack of internet access, lack of English literacy (Grade 5 level).

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Calgary Zone, Alberta Health Services Calgary Alberta Recruiting
Vita Diagnostics Calgary Alberta Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05900414 on ClinicalTrials.gov ↗ ← All trials in Canada