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Get the free study protocol for a randomized controlled trial - PMC

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P R O X Y Annual General Meeting of Members, June 8, 2019 I, ___, Member of Acupuncture Canada, Print Name in the province of ___ hereby appoint: Nimet Meghji, President[ ]or failing her,Catharine
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Start by clearly stating the objectives of the study.
02
Include a detailed description of the study design and methodology.
03
Provide information on study population, sample size, and inclusion/exclusion criteria.
04
Outline the procedures to be followed for data collection and analysis.
05
Address ethical considerations and ensure compliance with regulations and guidelines.
06
Include a detailed schedule of study activities and timelines.
07
Define the roles and responsibilities of key personnel involved in the study.
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Review and revise the protocol as needed based on feedback from stakeholders.

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Researchers conducting clinical trials or observational studies
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Funding organizations requiring a detailed plan for study conduct
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A study protocol is a document that outlines the objectives, design, methodology, statistical considerations, and organization of a study. It serves as a blueprint for conducting the research.
Typically, the principal investigator or the lead researcher of the study is required to file the study protocol, often in conjunction with their institution's research ethics board or regulatory body.
To fill out a study protocol, you should include sections such as the title of the study, objectives, background information, study design, methods, statistical analysis plan, and ethical considerations. Each section should be detailed and clearly written to guide the research process.
The purpose of a study protocol is to ensure that the research is conducted consistently and ethically, to provide a clear methodology for evaluating the results, and to comply with regulatory requirements.
The study protocol must report details such as the study title, objectives, methodology, participant recruitment strategies, data collection methods, and planned analyses, as well as ethical considerations and potential risks to participants.
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