A prospective trial with hospitals/health centres across 6 different European countries, being randomised to either a structured education programme as the intervention or no additional education as the control. To determine whether a comprehensive educational programme for healthcare professionals will increase the rate of appropriate stroke prevention and rhythm control therapy in patients with atrial fibrillation (AF) and adherence to Guidelines.
Prospective, parallel group, two-arm, unblinded, international, cluster-randomized controlled trial. Intervention arm: A 16-week blended learning programme targeting stroke prevention and rhythm control therapy at the healthcare professional level, with controlled assessments, a commitment to change plan, and reinforcement actions Control arm: No added education of healthcare professionals 70 centres with a cluster size of 25 patients; total estimated number of patients 1750. 8-12 weeks patient recruitment period at each centre; 16 weeks educational intervention period; primary \& secondary outcomes at 6-9 months post-randomisation; remote follow-up for clinical events (no new patient contact) at 18 months from randomisation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Enrollment
1,732
Randomization between two groups at site level. One cluster with education and one without.
Adherence to ESC Guidelines in Atrial Filbrillation
Full adherence to guidelines for stroke prevention rhythm control therapy
Time frame: 25 months per centre
Proportion of relevant guidelines adhered to
Proportion of relevant guidelines adhered to for stroke prevention and rhythm control
Time frame: 25 months per centre
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Nancy, Meurthe-et-Moselle (Lorraine), France
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Rouen, Normandy, France
CHU Rangueil
Toulouse, Occitanie, Haute-Garonne, France
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Poitiers, Poitou-Charentes, France
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Aix-en-Provence, Provence-Alpes-Côte d'Azur Region, France
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