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Protocol template (Protocol)rPreviewOnlyNNFoThis is a reprint of a Cochrane protocol, prepared and maintained by The Cochrane Collaboration and published in The Cochrane Library 2013, Issue 9 http://www.thecochranelibrary.comProtocol
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Step 1: Start by downloading the protocol template from the Cochrane website
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Step 2: Familiarize yourself with the sections and subheadings in the template
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Step 3: Begin filling out the protocol template by providing the title of your study
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Step 4: Include a brief summary or background information about the topic of your study
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Step 5: Clearly state your research question or objective in the designated section
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Step 6: Describe your study design, including the type of participants, interventions, and outcomes
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Step 7: Specify your intended methods for data collection and analysis
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Step 8: Provide a timeline or schedule for the different stages of your study
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Step 9: Include any references or citations relevant to your study
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Step 10: Review and revise your filled-out protocol template for accuracy and completeness
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Step 11: Save and submit your completed protocol template according to the Cochrane submission guidelines

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Researchers who are planning to conduct systematic reviews or meta-analyses
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It is a standardized form that outlines the methods and procedures for a research study in accordance with Cochrane guidelines.
All researchers conducting studies that will be included in Cochrane reviews are required to file a protocol template.
Researchers can fill out the protocol template by providing detailed information on the study design, objectives, methods, and analysis plan.
The purpose of the protocol template is to ensure transparency, consistency, and quality in research studies included in Cochrane reviews.
Information such as study aims, eligibility criteria, data collection methods, and analysis techniques must be reported on the protocol template.
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