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Prospective Research Study Protocol Template Study Protocol Title: Can A Prescribed Walking Program with or without Monitoring Impact Dizziness in the Older Adults? Study Sponsor: Florida Hospital Principal
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How to fill out prospective research study protocol

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How to fill out prospective research study protocol

01
Start by identifying the research study's objectives and research questions.
02
Develop a clear study design that outlines the methodology and procedures.
03
Determine the target population for the study and define the inclusion and exclusion criteria.
04
Create a detailed data collection plan, including the variables to be measured and the data sources.
05
Design the informed consent form and ensure it complies with ethical guidelines.
06
Develop a comprehensive data analysis plan, including statistical tests and software to be used.
07
Create a timeline for the study, considering recruitment, data collection, and analysis.
08
Draft the study protocol document, including all the necessary sections such as introduction, methods, ethics, data analysis, and references.
09
Review the draft protocol with the research team and make necessary revisions.
10
Obtain ethical approval from the relevant institutional review board or ethics committee.
11
Distribute the final protocol to all study personnel and ensure they understand their roles and responsibilities.
12
Implement the protocol and monitor the study closely to ensure compliance.
13
Keep a record of any protocol deviations or amendments.
14
Analyze the collected data according to the predefined analysis plan.
15
Interpret the results and draw conclusions based on the findings.
16
Prepare a comprehensive research study report, including the protocol, findings, and recommendations.

Who needs prospective research study protocol?

01
Prospective research study protocols are needed by researchers and research teams involved in conducting new research studies.
02
Academic institutions, research organizations, pharmaceutical companies, and government agencies often require protocols for obtaining funding or approvals.
03
Ethics committees and institutional review boards also need protocols to review and approve the research study.
04
Additionally, prospective research study protocols are essential for ensuring the study's validity, transparency, and replicability.
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Prospective research study protocol is a detailed plan outlining the objectives, design, methodology, and procedures for a research study that has not yet been conducted.
Researchers conducting the study are required to file the prospective research study protocol.
Prospective research study protocol can be filled out by providing detailed information about the study design, objectives, methodology, and procedures in the designated template.
The purpose of prospective research study protocol is to ensure transparency, consistency, and accountability in the conduct of research studies.
Prospective research study protocol must include information on study design, objectives, methodology, procedures, participant inclusion/exclusion criteria, data collection and analysis procedures, and ethical considerations.
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