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A structured telephone delivered intervention to reduce problem alcohol use (Ready2Change)Australian New Zealand Clinical Trials Registry ACTRN12618000828224. Preregistered on 16 May 2018. Statistical
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01
Begin by outlining the purpose of the study protocol.
02
Provide a detailed description of the study methodology and design.
03
Include information on the study population, including inclusion/exclusion criteria.
04
Clearly outline the study procedures and interventions.
05
Detail the data collection and analysis methods to be used.
06
Discuss ethical considerations and approval processes.
07
Include any potential risks and benefits for participants.
08
Clearly state the expected outcomes and objectives of the study.
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Researchers conducting clinical trials or scientific studies.
02
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Regulatory bodies and authorities responsible for approving research protocols.
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What is study protocol for a?
Study protocol for a is a detailed plan outlining the objectives, design, methodology, statistical considerations, and organization of a research study.
Who is required to file study protocol for a?
Researchers, investigators, or sponsors conducting the study are required to file the study protocol for a.
How to fill out study protocol for a?
To fill out a study protocol for a, one must provide detailed information on the study design, objectives, methodology, statistical analysis plan, and organizational structure.
What is the purpose of study protocol for a?
The purpose of a study protocol for a is to ensure transparency, consistency, and integrity in research, and to provide a roadmap for conducting the study.
What information must be reported on study protocol for a?
Information such as study objectives, design, methodology, statistical analysis plan, and organizational details must be reported on the study protocol for a.
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