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Aalborg UniversitetCluster randomized controlled trial of screening for atrial fibrillation in people aged 70 years and over to reduce stroke: protocol for the pilot study for the SAFER trial Williams,
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How to fill out cluster randomised controlled trial

01
Identify clusters: Determine the groups or clusters that will be randomly assigned to receive different interventions.
02
Obtain informed consent: Obtain approval from ethical committees and informed consent from participants in each cluster.
03
Randomly allocate clusters: Use a randomization method to assign each cluster to a specific intervention group.
04
Implement interventions: Carry out the interventions as planned in each cluster.
05
Collect data: Collect data on outcomes of interest from participants in each cluster.
06
Analyze data: Analyze the collected data using statistical methods to evaluate the effectiveness of the interventions.
07
Report findings: Summarize the results of the trial and publish them in scientific journals or present them at conferences.

Who needs cluster randomised controlled trial?

01
Researchers conducting studies in community settings where individuals are naturally grouped into clusters.
02
Policy makers looking to implement interventions at a group level rather than individual level.
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Public health officials aiming to evaluate the impact of interventions on populations rather than individuals.
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Organizations interested in comparing the effectiveness of different interventions across multiple sites or regions.
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Cluster randomised controlled trial is a type of study design where groups of participants are randomly allocated to different interventions, rather than individuals.
Researchers or research teams conducting the trial are required to file cluster randomised controlled trial.
To fill out a cluster randomised controlled trial, researchers need to carefully design the study, gather data from clusters, analyze the results, and report findings according to research standards.
The purpose of cluster randomised controlled trial is to assess the effectiveness of interventions at the group level, rather than individual level.
Information such as study design, interventions, outcomes, statistical analysis, results, and conclusion must be reported on cluster randomised controlled trial.
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