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A comprehensive checklist and proforma detailing the reporting standards for randomized controlled trials, including requirements for trial design, methodology, outcomes, and participant information.
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How to fill out consort checklist and annexures
How to fill out consort checklist and annexures
01
Obtain the CONSORT checklist from a reliable source.
02
Review each item on the checklist to understand its requirements.
03
Prepare a draft of your study report or protocol that includes all relevant details.
04
Go through the checklist point by point and ensure each item is addressed in your document.
05
Provide concise explanations or data for each required item, highlighting your study’s methods, results, and conclusions.
06
For annexures, ensure you have all supplementary documents ready, including ethical approval, consent forms, and data collection tools.
07
Cross-check your annexures to ensure they correspond with the items listed in the main checklist.
08
Review your completed checklist and annexures to ensure clarity and completeness.
09
Submit the checklist and annexures along with your manuscript or protocol.
Who needs consort checklist and annexures?
01
Researchers conducting randomized controlled trials.
02
Authors preparing manuscripts for publication in scientific journals.
03
Study sponsors and ethics review boards.
04
Regulatory authorities reviewing trial protocols.
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What is consort checklist and annexures?
The CONSORT checklist is a tool used to ensure that clinical trial reports are transparent and complete. It consists of a list of essential items that should be included when reporting results of randomized controlled trials. Annexures typically include supplementary materials or additional information that support the main report.
Who is required to file consort checklist and annexures?
Researchers and authors of randomized controlled trials are required to file the CONSORT checklist and annexures when submitting their manuscripts for publication in medical journals that endorse the CONSORT guidelines.
How to fill out consort checklist and annexures?
To fill out the CONSORT checklist, researchers should review each item listed and provide the corresponding information in their manuscript. Each item should be addressed, with explanations or page references included in the checklist. Annexures should be prepared to include any additional methodology or data necessary to substantiate the study findings.
What is the purpose of consort checklist and annexures?
The purpose of the CONSORT checklist and annexures is to improve the quality and transparency of reporting in clinical trials. They help ensure that all relevant information is disclosed and facilitate critical appraisal and replication of studies.
What information must be reported on consort checklist and annexures?
The information reported on the CONSORT checklist includes trial design, participant flow, recruitment, baseline data, interventions, outcomes, sample size, randomization, blinding, statistical methods, and other relevant details. Annexures may include additional analyses, ethical considerations, or study protocols.
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