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UNIVERSITY OF CALGARY CONSENT TO PARTICIPATE IN RESEARCHTITLE: Blinded Randomized trial of Anticoagulation to prevent Ischemic stroke and Neurocognitive Impairment in Atrial Fibrillation Pharmacogenomic
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01
Define the study population and eligibility criteria for participants.
02
Obtain informed consent from all participants before enrolling them in the study.
03
Randomly assign participants to either the treatment group or the control group, ensuring that the assignment is blinded to reduce bias.
04
Ensure that the randomization process is appropriately documented.
05
Administer the treatment or intervention to the treatment group, while providing a placebo or no treatment to the control group.
06
Collect baseline data for all participants on relevant outcomes and demographics.
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Monitor participants throughout the study to track adherence and any outcomes of interest.
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Analyze the data using appropriate statistical methods to compare the outcomes between the two groups.
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Report the findings in accordance with relevant guidelines for randomized controlled trials.

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The term 'brain af blinded randomized' does not pertain to standard terminology and may refer to a specific study or method involving randomization in clinical trials, particularly in relation to brain applications.
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Key information typically includes study objectives, study design, sample size, blinding methods, randomization procedures, and outcomes measured.
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