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This document outlines the study protocol for the Australian National Child Hearing Health Outcomes Registry (ANCHOR), a program aimed at connecting and collecting child hearing health information to improve service delivery and outcomes for deaf and hard of hearing children in Australia. It emphasizes community engagement, systematic data collection, and the development of a Core Outcome Set to drive effective care and research.
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01
Start with the title of the study at the top of the form.
02
Provide a brief introduction, including the background and significance of the study.
03
Clearly define the objectives or aims of the study.
04
Describe the study design, specifying whether it is observational, experimental, etc.
05
Outline the study population, including inclusion and exclusion criteria.
06
Detail the methods of data collection and analysis you plan to use.
07
Include a timeline of the study phases and key milestones.
08
Specify the roles and responsibilities of the research team members.
09
Include ethical considerations and any necessary approvals from relevant boards.
10
Review the form for completeness and clarity before submission.

Who needs study protocol - form?

01
Researchers conducting clinical trials or other studies.
02
Research institutions that require formal documentation of study protocols.
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Ethics review boards that evaluate and approve research proposals.
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Funding agencies that require detailed study plans for grant applications.
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A study protocol form is a document that outlines the plan for a research study, including the objectives, design, methodology, statistical considerations, and organization of the study.
Researchers conducting clinical trials, academic institutions, and sponsors of research studies are typically required to file a study protocol form.
To fill out a study protocol form, researchers should provide detailed information regarding the study objectives, methods, participant criteria, interventions, data collection procedures, and analysis plans, adhering to any specific guidelines provided by regulatory bodies.
The purpose of the study protocol form is to ensure clarity and consistency in research planning, facilitate ethical review, guide the conduct of the study, and improve the reliability and validity of findings.
The study protocol form must report information such as the study title, objective, background, methodology, sample size, participant selection criteria, intervention details, data management processes, ethical considerations, and statistical analysis plan.
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