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This document outlines the study protocol for the development, implementation, and evaluation of a digital triage tool aimed at improving the recognition and treatment of sepsis in children. It details
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How to fill out research study protocol

01
Title: Provide a clear and concise title for the study.
02
Introduction: Write a brief introduction including background information and the rationale for the study.
03
Objectives: Clearly state the objectives and goals of the research.
04
Study Design: Describe the type of study (e.g., observational, experimental) and the design considerations.
05
Methodology: Outline the methods for data collection, including participant selection, intervention details, and data analysis plans.
06
Ethical Considerations: Include information on how ethical standards will be maintained and how informed consent will be obtained.
07
Timeline: Provide a timeline for the study, including key milestones.
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Budget: Include an estimated budget for the study, detailing costs associated with personnel, materials, and other expenses.
09
References: List any references or prior studies that support the proposed research.

Who needs research study protocol?

01
Researchers conducting scientific studies to ensure compliance and clarity in their research.
02
Ethics review boards to assess the ethical implications of the study.
03
Funding organizations that require a clear research plan for grant applications.
04
Institutional Review Boards (IRBs) for monitoring the safety and ethics of research involving human subjects.
05
Study participants to understand the purpose and methods of the research they are involved in.
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A research study protocol is a detailed plan that outlines the objectives, design, methodology, statistical considerations, and organization of a research study. It serves as a guide for conducting the research.
Researchers, including principal investigators and sponsors, are typically required to file a research study protocol with regulatory bodies and ethics committees before initiating a clinical or scientific study.
To fill out a research study protocol, researchers must follow prescribed guidelines that typically include specifying study objectives, eligibility criteria, methodology, statistical analysis plan, and data management procedures. It is essential to adhere to institutional and regulatory requirements.
The purpose of a research study protocol is to ensure that the study is conducted systematically and ethically, providing a clear roadmap for researchers and protecting the rights and well-being of participants.
A research study protocol must report key information such as study objectives, design, methods, participant eligibility criteria, recruitment strategies, data collection procedures, statistical analysis plan, funding sources, and potential ethical considerations.
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