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BMJ Open FO Journal:Manuscript Article Type:Date Submitted by the Author:bmjopen2016014506Research29Sep2016eeComplete List of Authors:BMJ OpenwieevrrBlair, Peter; University of Bristol, School Of
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How to fill out feasibility cluster randomised controlled

01
Identify the research question or objective of the study.
02
Determine the appropriate sample size and number of clusters.
03
Randomly allocate the clusters to either the intervention or control group.
04
Collect baseline data on the participants in each cluster.
05
Implement the intervention in the allocated clusters.
06
Monitor and evaluate the outcomes or effects of the intervention.
07
Analyze the data and draw conclusions on the feasibility of the intervention.
08
Report the findings and recommendations of the study.

Who needs feasibility cluster randomised controlled?

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Researchers conducting pilot studies or feasibility studies for new interventions.
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Healthcare professionals interested in assessing the feasibility of implementing a new treatment or intervention in a specific population or setting.
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Policy makers and decision makers who require evidence on the feasibility and potential effectiveness of new interventions before implementing them on a larger scale.
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A feasibility cluster randomised controlled trial is a type of research study that assesses the practicality of implementing a randomized controlled trial within a specific context or population. It helps determine whether the proposed study is feasible and identifies potential challenges.
Researchers or institutions conducting feasibility cluster randomised controlled trials are typically required to file relevant documentation with ethics boards or regulatory authorities to ensure compliance with research standards.
Filling out a feasibility cluster randomised controlled study involves providing detailed documentation on the study design, methodology, target population, sampling strategy, intervention details, and ethical considerations. Each section must be completed according to the guidelines set by the regulatory authority.
The purpose of a feasibility cluster randomised controlled trial is to evaluate whether a larger scale randomized controlled trial can be effectively conducted. It assesses logistical aspects, potential participant recruitment, intervention delivery, and data collection methods.
Information that must be reported includes study objectives, methodology, participant demographics, recruitment strategies, intervention details, outcome measures, and any ethical considerations related to the trial.
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