Actively Recruiting
STROKESTOP III - Optimized Method for Atrial Fibrillation Screening
Led by Danderyd Hospital · Updated on 2024-05-06
2200
Participants Needed
2
Research Sites
112 weeks
Total Duration
On this page
Sponsors
D
Danderyd Hospital
Lead Sponsor
K
Karolinska Institutet
Collaborating Sponsor
AI-Summary
What this Trial Is About
Atrial fibrillation is the most common sustained cardiac arrhythmia affecting more than 3% of the adult population. The symptoms of atrial fibrillation can range from asymptomatic to debilitating. It can be permanent in its nature, but also paroxysmal with only short bursts of atrial fibrillation randomly occurring and can therefore remain unnoticed. Atrial fibrillation increases the risk of stroke five fold if left untreated. Screening for atrial fibrillation in elderly populations above age 65 years can result in detection of new atrial fibrillation cases ranging from 0,5% new AF with a single time-point ECG, up to 30% AF if an implantable loop recorder is inserted for 3 years. Currently opportunistic screening using pulse palpation, or a single time-point ECG is recommended by the European Society of Cardiology guidelines. Systematic screening in individuals aged 75 or above, or at a high stroke risk should be considered. Overall, participation in systematic atrial fibrillation screening trials has been shown to be relatively low with almost 50% non-participants. Participants are generally healthier, with higher socioeconomic status, hence the ones who would potentially benefit the most remain absent. Opportunistic screening has shown promising results with higher participation rates and the possibility of better outreach. There is a lack of data from randomized trials on the difference in participation rates in systematic and opportunistic screening approaches when screening with prolonged ECG monitoring.
CONDITIONS
Official Title
STROKESTOP III - Optimized Method for Atrial Fibrillation Screening
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Individuals aged 75 or 76 years in 2024 (born 1948 or 1949)
- Must live in the Värmland region
- Must be registered at a primary care facility with at least 200 people aged 75 or 76
You will not qualify if you...
- Currently using oral anti coagulation treatment (OAC)
- Have contraindications to OAC treatment
- Have known and treated atrial fibrillation
- Unable to provide consent to participate
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Karolinska Institutet, Dept Med H
Stockholm, Sweden, 141 86
Not Yet Recruiting
2
Region Värmland
Värmland, Sweden
Actively Recruiting
Research Team
E
Emma Svennberg, MD PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
2
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