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Table 2: CONSORT 2010 checklist when reporting a cluster randomized trial Section/Toxicity Nonstandard Checklist overextension for cluster designs Page No *1aIdentification as a randomized trial in

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How to fill out consort 2010 statement extension

01

To fill out the CONSORT 2010 statement extension, follow these steps:

02

Start with the title section: Provide the title of your study and any other necessary details, such as the authors' names and affiliations.

03

Move on to the abstract section: Summarize the study objectives, methods, results, and conclusions in a concise manner.

04

Fill in the introduction section: Clearly state the background and rationale for the study.

05

Provide details about the trial design and methods, including the participants, interventions, and outcomes.

06

Specify the randomization process, including any blinding procedures.

07

Describe the statistical methods used for data analysis.

08

Present the results section, including both primary and secondary outcomes.

09

Discuss the limitations of the study and any potential biases.

10

Conclude with a summary of the findings and their implications.

11

Finally, provide references to any related publications or studies.

12

Remember to refer to the CONSORT 2010 guidelines for more detailed instructions on each section.

Who needs consort 2010 statement extension?

01

The CONSORT 2010 statement extension is necessary for researchers and authors who are conducting and reporting clinical trials. It helps ensure transparency and standardized reporting of trial protocols and results, facilitating the evaluation and comparison of studies in the field of medicine.

02

Journals, publishers, and reviewers also benefit from CONSORT 2010 statement extension as it enables them to assess the quality and completeness of submitted manuscripts. Adhering to the extension may be required by certain journals or funding agencies for publication or grant consideration. Ultimately, anyone involved in the design, execution, or publication of clinical trials can benefit from the use of CONSORT 2010 statement extension.

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What is consort statement extension to?

Consort statement extension is an extension to the CONSORT (Consolidated Standards of Reporting Trials) statement, which provides guidelines for reporting randomized controlled trials.

Who is required to file consort statement extension to?

Researchers and authors conducting randomized controlled trials are required to file consort statement extensions.

How to fill out consort statement extension to?

Consort statement extensions should be filled out following the guidelines provided in the CONSORT statement.

What is the purpose of consort statement extension to?

The purpose of consort statement extension is to improve the transparency and completeness of reporting of randomized controlled trials.

What information must be reported on consort statement extension to?

Consort statement extension should include details on trial methodology, participant recruitment, randomization procedures, and statistical analysis methods.

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