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The SafeBoosCIII two year followup (Safeguarding the brain of our smallest children)Dear Parents, This is to ask if we may use the health care records of your child for research. We are contacting
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Start by clearly defining the research question or objective of the study.
02
Specify the study design, including the methods and procedures to be used.
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Provide a detailed description of the study population and inclusion/exclusion criteria.
04
Outline the data collection methods and tools to be used.
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Address ethical considerations and include a plan for obtaining informed consent.
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Who needs a study protocol for?

01
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A study protocol is a detailed plan that outlines the objectives, design, methodology, and statistical considerations of a research study.
Researchers and institutions that conduct clinical trials or research studies are typically required to file a study protocol.
To fill out a study protocol, one should provide comprehensive details about the study design, objectives, participant selection criteria, data collection methods, and any ethical considerations.
The purpose of a study protocol is to ensure a systematic approach to research, provide a framework for conducting the study, and facilitate review and approval by regulatory bodies.
A study protocol must report information including the study title, objectives, methodology, participant criteria, intervention details, data analysis plan, and ethical considerations.
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