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Open AccessProtocolCluster randomized controlled trial of a financial incentive for mothers to improve breastfeeding in areas with low breastfeeding rates: the NOSH study protocol Clare Elton,1 Mark
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01
Identify the clusters: Start by identifying the group or clusters on which the randomization will be applied.
02
Define the sample size: Determine the number of clusters and individuals to include in the study.
03
Randomize clusters: Randomly assign each cluster to either the control group or the intervention group.
04
Obtain consent: Seek consent from individuals within the selected clusters to participate in the study.
05
Collect baseline data: Gather relevant data from both the control and intervention group before implementing any interventions.
06
Implement the intervention: Apply the intervention or treatment to the clusters in the intervention group.
07
Collect follow-up data: Continuously collect data from both groups to evaluate the impact of the intervention.
08
Analyze the data: Use appropriate statistical methods to analyze the collected data and determine the effectiveness of the intervention.
09
Draw conclusions: Interpret the results and draw conclusions based on the findings of the study.

Who needs cluster randomised controlled trial?

01
Cluster randomised controlled trials are beneficial for researchers and policymakers who want to evaluate the effectiveness of interventions or treatments at a group or cluster level.
02
They are commonly used in public health studies, educational research, community-based interventions, and social science research.
03
These trials are especially useful when individual randomization is not feasible or when the intervention is expected to have an impact on the entire cluster or group rather than individuals within it.
04
By using cluster randomised controlled trials, researchers can gather evidence on the effectiveness of interventions in real-world settings and make informed decisions about implementing them on a larger scale.
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A cluster randomised controlled trial is a type of research design where groups of individuals, rather than individuals themselves, are randomly assigned to different treatments or interventions.
Researchers conducting clinical trials or studies involving groups of individuals.
Researchers need to carefully plan the study design, randomise clusters of participants, collect data, and analyze results according to predetermined protocols.
The purpose of cluster randomised controlled trials is to evaluate the effectiveness of interventions or treatments at the group level, rather than individual level, providing more accurate and generalizable results.
Researchers must report details of the study design, randomisation process, interventions, outcomes measures, data analysis, and results.
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2015 2016 uk randomised nancial nhs bmj relton bmjopen doi e010158 prevalence acceptability subgroup dened crct ofce specic whelan renfrew organisational ve gure shefeld covariates pokhrel necrotising permissions comparator funders rotherham postbirth cle

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