Randomized Evaluation of Decision Support Interventions for Atrial Fibrillation
Completed · Not applicable
Conditions studied: Atrial Fibrillation
In brief
This study will compare the effectiveness of the use of a Patient Decision Aid (PDA) and an Encounter Decision Aid (EDA) on Shared Decision Making (SDM) and health outcomes for at-risk participants with Atrial Fibrillation (AF) at 6 study sites. We hypothesize the combination of the PDA and EDA will be more effective in promoting high-quality SDM and in adoption of and adherence to anticoagulation than either tool alone.
Key facts
- Study ID
- NCT04357288
- Run by
- University of Utah
- People needed
- 1117
- Starts
- 2020-12-16
- Expected to finish
- 2024-09-20
- Last updated by the study team
- 2025-01-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults (18 and older)
- Are diagnosed with Atrial Fibrillation
- Are aware they have been diagnosed with Atrial Fibrillation
- Participants with additional risk of thromboembolic events (CHA2DS2-VASc scores ≥ 1 in men and ≥ 2 in women)
You may not qualify if…
- Participants deemed by their clinician or research personnel to be ineligible for consideration of taking or of foregoing anticoagulation
- Have deficits in cognitive abilities or sensory input
- Have a language barrier significant enough to impede shared decision making and/or the provision of written informed consent.
- Clinician Participants -
- Inclusion Criteria:
- All clinicians (MDs, NP/PAs, PharmDs, APPs, etc.) that are responsible for the modality of Anticoagulation in eligible AF patients at participating sites, without exclusion.
Where it is running
- University of Alabama at Birmingham — Birmingham, Alabama, United States
- Northwestern University — Chicago, Illinois, United States
- University of Michigan — Ann Arbor, Michigan, United States
- The Mayo Clinic — Rochester, Minnesota, United States
- Vanderbilt University — Nashville, Tennessee, United States
- University of Utah Health — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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