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Downloaded from http://bmjopen.bmj.com/ on June 28, 2016, Published by group.bmj.com Open Access Protocol Cluster randomized controlled trial of a financial incentive for mothers to improve breastfeeding
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How to fill out a cluster randomised controlled trial (RCT):

01
Identify the research question and objectives of the study.
02
Determine the appropriate sample size and power calculation for the trial.
03
Select the clusters that will be part of the trial, ensuring they are similar and representative of the target population.
04
Randomly allocate clusters to either the intervention or control group.
05
Develop the intervention protocol and ensure it is properly implemented in the intervention clusters.
06
Collect baseline data on all relevant variables.
07
Implement the interventions or treatments in the appropriate clusters over the specified time period.
08
Collect follow-up data on the outcome measures of interest.
09
Analyze the data using appropriate statistical methods, accounting for the clustering effect.
10
Interpret the results and draw conclusions based on the study findings.

Who needs a cluster randomised controlled trial:

01
Researchers and scientists conducting studies in fields such as medicine, public health, education, and social sciences.
02
Organizations seeking to evaluate the effectiveness of interventions or treatments at a group or community level.
03
Policy-makers and government agencies interested in evidence-based decision-making.
04
Funding bodies and grant providers looking to support research in a systematic and rigorous manner.
05
Practitioners in healthcare, education, or public policy who want to base their practices on robust scientific evidence.
Note: The need for a cluster randomised controlled trial may vary depending on the research question and context. It is essential to consider the advantages and limitations of this study design before deciding if it is appropriate for a specific situation.
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A cluster randomised controlled trial is a type of study design in which groups of participants, rather than individuals, are randomly allocated to different interventions or control groups.
Researchers conducting studies that involve cluster randomised controlled trials are required to file the necessary documentation and reports.
To fill out a cluster randomised controlled trial, researchers must carefully plan the intervention, randomisation process, data collection methods, and analysis plan according to study protocols.
The purpose of a cluster randomised controlled trial is to evaluate the effectiveness of interventions at the group level, rather than individual level, in order to account for potential biases and increase statistical power.
Information that must be reported on a cluster randomised controlled trial includes study design, randomisation procedures, intervention details, outcome measures, statistical analyses, and results.
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