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Protocol: Consort extension to the stepped wedge cluster randomized trial July 12, 2014Protocol: Consort extension to stepped wedge cluster randomized controlled trial Version 1Investigators Karla
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How to fill out protocol consort extension to?

01
Start by reviewing the requirements of the PROTOCOL CONSORT extension and familiarize yourself with its guidelines. This will help you understand what information needs to be included in the protocol extension.
02
Begin filling out the protocol consort extension by providing the necessary details about the study design. This includes information about the study objectives, study type, and randomization methods, among others. Make sure to follow the specific formatting requirements outlined in the extension guidelines.
03
Next, move on to describing the participants involved in the study. Include details such as eligibility criteria, recruitment methods, and the number of participants in each study arm. This section should be clear and comprehensive to ensure transparency and reproducibility.
04
Provide a detailed description of the interventions or treatments being studied. Include information such as the dosage, frequency, and duration of the intervention, as well as any control groups or comparison interventions. This will help readers understand the context of the study and how the interventions were implemented.
05
Ensure that you include information on the primary and secondary outcomes of the study. Specify the outcome measures used, how they were assessed, and the time points at which the assessments were conducted. This section should be structured and clear, making it easy for readers to understand the study's objectives and results.
06
Finally, include any necessary additional information such as statistical analysis methods, adverse events reporting, and any relevant ethical considerations. Make sure to follow the specific guidelines provided in the protocol consort extension to ensure completeness and accuracy.

Who needs protocol consort extension to?

01
Researchers who are conducting clinical trials or interventional studies can benefit from using the protocol consort extension. This extension helps ensure that the study protocol is well-documented and adheres to the CONSORT (Consolidated Standards of Reporting Trials) guidelines.
02
Journal editors and peer reviewers may also find the protocol consort extension useful when evaluating research papers. This extension helps improve the transparency and reproducibility of study protocols, making it easier for editors and reviewers to assess the study's quality and validity.
03
Funding agencies and regulatory bodies may require researchers to include a protocol consort extension as part of their grant applications or regulatory submissions. This ensures that the study protocol meets certain standards and promotes rigorous research practices.
In conclusion, filling out the protocol consort extension requires careful attention to detail and adherence to the guidelines provided. Researchers, editors, reviewers, funding agencies, and regulatory bodies can all benefit from utilizing the protocol consort extension to ensure transparent and reproducible study protocols.
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Protocol consort extension is protocol extension to the study protocol.
The principal investigator is typically required to file protocol consort extension.
Protocol consort extension can be filled out by providing all the necessary information and documentation required.
The purpose of protocol consort extension is to update and extend the existing study protocol.
The information reported on protocol consort extension may include changes to study design, objectives, methodology, and endpoints.
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