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Date and version No: 07.04.2020 version 2.0Trial Title: Platform Randomized trial of Interventions against COVID-19 In older people Internal Reference Number / Short title: PRINCIPLE Ethics Ref: 20/SC/0158 IRAS
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Start by gathering all the necessary information and materials for the platform randomised trial.
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Identify the specific research question or objective that the trial aims to address.
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Develop a clear protocol outlining the trial design, participants, interventions, and outcomes.
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Randomize the participants into different groups using a platform randomized approach.
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Implement the interventions or treatments according to the assigned groups.
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Collect and record data on the outcomes of interest for each participant.
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Analyze the data using appropriate statistical methods to evaluate the efficacy or effectiveness of the platform.
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Interpret the results 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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Share the findings with relevant stakeholders and contribute to the advancement of knowledge in the field.

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Researchers and scientists conducting studies or experiments using a platform-based approach.
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A platform randomised trial is a type of clinical trial that evaluates multiple interventions or treatments simultaneously within the same framework, allowing for comparisons between them in a flexible and adaptive manner.
Researchers and institutions conducting platform randomised trials are typically required to file the necessary documentation and reports to regulatory bodies or ethics committees, depending on the jurisdiction.
Filling out a platform randomised trial typically requires providing details on the trial's design, interventions, participant eligibility criteria, statistical analysis plans, and expected outcomes in specified forms or templates provided by regulatory authorities.
The purpose of platform randomised trials is to efficiently evaluate the effectiveness of multiple treatments or interventions against a common control, ultimately leading to better-informed clinical decisions and improved patient outcomes.
Key information to be reported includes the trial design, intervention details, participant demographics, outcome measures, data analysis methods, and results, including safety and efficacy findings.
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