N/A
N=1,145
Integrated Management Program Advancing Community Treatment of Atrial Fibrillation
Atrial Fibrillation
Bottom Line
View on ClinicalTrials.gov: NCT01927367 ↗Enrolled (actual)
1,145
Serious AEs
1.4%
Results posted
Sep 2020
Primary outcome: Primary: Number of Participants With Cardiovascular Hospitalization and AF-related Emergency Department Visits — 118; 130 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Clinical Decision Support System for AF (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Jafna L Cox
- Primary completion
- Nov 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants With Cardiovascular Hospitalization and AF-related Emergency Department Visits |
118; 130 | — |
| SECONDARY Number of Participants With AF-related Emergency Department Visits |
78; 96 | — |
| SECONDARY Process of Care |
— | — |
| SECONDARY Health Related Quality of Life |
— | — |
| SECONDARY Costs |
— | — |
| SECONDARY Cost Effectiveness |
— | — |
| SECONDARY Number of Participations With CV Hospitalizations |
40; 26 | — |
Summary
Research Question: Among community-based patients with AF, does providing an integrated Clinical Decision Support System (CDSS) to providers and patients improve process of care and clinical outcomes, and decrease the healthcare costs and resource utilization over 12 months, as compared to usual care?
Intervention: A web-based clinical decision support system, computerizing the Canadian AF clinical guidelines, to support primary care providers and patients in optimizing and standardizing AF care.
Eligibility Criteria
Inclusion Criteria
- Age >/= 18 years (no max age limit)
- Confirmed atrial fibrillation.
- Able to provide informed consent in English.
Exclusion Criteria
- Patients unable to provide informed consent.
- Patients who are not expected to be alive at the end of the 12 month follow up.
Data sourced from ClinicalTrials.gov (NCT01927367). 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.