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Platform Randomized trial of Interventions against COVID-19 In older people PRINCIPLE REC Number: 20/SC/058 Chief Investigator:IRAS Number: 281958EudraCT Number:202000120922Professor Christopher Butler Participant
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To fill out the platform randomised trial of, follow these steps:
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Start by gathering all the necessary information and documentation required for the trial.
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Identify the platform on which the trial will be conducted.
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Develop a clear and detailed plan for the trial, including the objectives, procedures, and expected outcomes.
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Design the trial protocol and obtain any necessary approvals or permissions from relevant authorities or ethics committees.
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Recruit participants who meet the eligibility criteria for the trial.
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Randomly assign participants to either the intervention or control group using a platform-based randomisation method.
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Implement the trial according to the protocol, ensuring that all procedures are followed accurately and consistently.
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Monitor and collect data throughout the trial period, using the platform to track participant progress and outcomes.
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Analyze the collected data using appropriate statistical methods to determine the effectiveness and safety of the intervention.
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Interpret the results of the trial and draw conclusions based on the findings.
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Prepare a comprehensive report summarizing the trial methodology, results, and conclusions.
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Publish or present the findings to relevant stakeholders and the scientific community.

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Platform randomised trial is a type of clinical trial design where multiple treatments are tested within the same trial.
Researchers and organizations conducting the clinical trial are required to file platform randomised trial.
Platform randomised trial forms can be filled out online through the designated platform or submitted via email or mail.
The purpose of platform randomised trial is to compare the effectiveness of multiple treatments in a single trial setting.
Information such as study protocol, treatment arms, inclusion criteria, exclusion criteria, and statistical analysis plan must be reported on platform randomised trial.
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