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Position DescriptionYouth and Family Coach Wesley Youth Hope October 2020AgreementSigned ManagerSigned EmployeeDateDatePosition Title ManagerManagers initials ___Employees initials ___Page 1 of 8Youth
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How to fill out extending a randomized trial

01
Review the protocol of the original randomized trial to understand the objectives and methods.
02
Determine the key outcomes that need to be assessed in the extended trial.
03
Contact the principal investigator of the original trial to discuss the extension and gain their approval.
04
Develop a study protocol for the extended trial, including any modifications or additions to the original protocol.
05
Obtain ethical approval for the extended trial from the relevant research ethics committee.
06
Recruit participants for the extended trial using similar methods to the original trial.
07
Collect and analyze data according to the study protocol.
08
Compare the results of the extended trial to the original trial and draw conclusions based on the findings.

Who needs extending a randomized trial?

01
Researchers looking to further investigate the findings of a randomized trial.
02
Funders interested in supporting additional research on a particular intervention or treatment.
03
Policy makers seeking more evidence to inform decision-making.
04
Healthcare providers looking to improve patient care based on research outcomes.
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Extending a randomized trial refers to prolonging the duration of a clinical trial to gather more data or reach a more robust conclusion.
The principal investigator or sponsor of the clinical trial is typically required to file for an extension.
To fill out an extension for a randomized trial, the principal investigator or sponsor must provide justification for the extension, outline the new timeline, and obtain any necessary approvals.
The purpose of extending a randomized trial is to ensure sufficient data collection, address unexpected issues that may have impacted the original timeline, or conduct additional analyses.
The extension request should include the reasons for the extension, revised study timeline, impact on participants, and any changes to study procedures or endpoints.
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