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Clinical Trial Protocol Physiological, Psychological, Psychiatric, Surgical or Health Interventions UNSW REC Title: Improving childhood sleep: the bedrock of depression prevention January 2023, Version
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01
Start by carefully reading the study protocol template provided by your institution or sponsor.
02
Fill out the sections related to study background and rationale, study objectives, inclusion and exclusion criteria, study procedures, data collection methods, and statistical analysis plan.
03
Make sure to provide detailed information about the study design, sample size calculation, study population, interventions, outcome measures, and ethical considerations.
04
Check for any specific requirements or guidelines regarding the format and content of the study protocol before finalizing and submitting it for approval.
Who needs study protocol of a?
01
Researchers conducting clinical trials or observational studies
02
Investigators applying for research grants
03
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04
Regulatory authorities assessing the safety and efficacy of new interventions
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What is study protocol of a?
A study protocol is a document that outlines the plan for a research study, detailing the objectives, methodology, and statistical considerations.
Who is required to file study protocol of a?
Researchers and institutions conducting studies that require ethical review and regulatory approval are required to file a study protocol.
How to fill out study protocol of a?
To fill out a study protocol, one must follow the provided guidelines, ensuring all sections, including objectives, methods, and safety considerations, are completed accurately.
What is the purpose of study protocol of a?
The purpose of a study protocol is to provide a clear and detailed plan for the research study, ensuring consistency and adherence to regulatory standards.
What information must be reported on study protocol of a?
The study protocol must report information such as study objectives, methodology, participant criteria, data collection methods, and ethical considerations.
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