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Cluster randomized controlled trial of a peer support program for people with diabetes: Study protocol for the Australasian peers for progress study This is the Published version of the following
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How to fill out cluster randomized controlled trial

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Step 1: Identify the clusters for the study. This could be a group of schools, hospitals, or communities that can be randomly assigned
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Step 2: Randomly assign the clusters to either the treatment group or the control group
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Step 3: Obtain informed consent from participants within each cluster
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Step 4: Implement the intervention or treatment in the treatment group
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Step 5: Collect data from both the treatment and control groups
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Step 6: Analyze the data to determine the effectiveness of the intervention
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Step 7: Draw conclusions based on the results and report the findings

Who needs cluster randomized controlled trial?

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Researchers who are studying interventions that are best implemented at a group or community level.
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Organizations or institutions interested in evaluating the impact of interventions on a larger population.
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Policy makers who need evidence to inform decision-making at a community or group level.
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A cluster randomized controlled trial is a type of experimental research design where groups, or clusters, rather than individual participants, are randomized to receive different interventions, allowing researchers to evaluate the effects of the interventions on the whole cluster.
Researchers or institutions conducting cluster randomized controlled trials are typically required to file the necessary documents with relevant regulatory bodies to ensure compliance with ethical and scientific standards.
Filling out a cluster randomized controlled trial involves providing detailed information about the study design, objectives, interventions, setting, participant criteria, and analytical methods, usually in a prescribed format provided by a regulatory body.
The purpose of a cluster randomized controlled trial is to evaluate the effectiveness of interventions implemented at the group level, which can account for intra-cluster correlation and improve the feasibility of interventions in real-world settings.
The report must include details such as study design, participant characteristics, randomization methods, implementation of interventions, outcome measures, statistical analysis plan, and ethical considerations.
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