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RESERVED FOR THE JCR IRB JCR IRB STAMP.APPROVED 31/Jul/2020PLEASE DON'T MOVE.CONSENT TO TAKE PART IN A RESEARCH STUDY TITLE: The International Diabetes Closed Loop (idol) trial: A Randomized Crossover
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Determine the research question or hypothesis that will be tested in the trial.
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Design the trial with a well-defined protocol including eligibility criteria, randomization process, treatment allocation, and outcome measures.
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Obtain ethical approval from an Institutional Review Board or Ethics Committee.
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Recruit participants and obtain informed consent.
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Randomly assign participants to treatment groups.
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A randomized trial is a type of scientific study in which participants are randomly assigned to different groups to receive different interventions or exposures.
Researchers conducting clinical trials are required to file a randomized trial.
A randomized trial can be filled out by following the specific protocol and guidelines set by the research institution or governing body.
The purpose of a randomized trial is to evaluate the effectiveness and safety of interventions or treatments in a systematic and unbiased way.
Information such as study design, participant characteristics, interventions, outcomes, and results must be reported on a randomized trial.
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