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Fall 2016 Fiscal Clinician Application Basketball 2016 Application Aquatic and Motor Development Program September 21st; 28th; October 5th; 12th; (Motor) October 19th; 26th ; November 2nd & 16th (Aquatic) Program
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How to fill out randomized clinical trial of

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Develop a clear research question or hypothesis that you want to investigate through the randomized clinical trial.
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Design the trial by determining the eligibility criteria for participants, the interventions or treatments that will be compared, and the outcomes that will be assessed.
03
Obtain ethical approval and funding for the trial.
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Recruit participants who meet the eligibility criteria and obtain informed consent from them.
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Randomize participants into different groups, ensuring that the allocation is unbiased and that the groups are similar in terms of important characteristics.
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Implement the interventions or treatments according to the assigned groups.
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Monitor and collect data on the outcomes of interest for each participant.
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Analyze the data using appropriate statistical methods to determine the effectiveness and safety of the interventions or treatments.
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Report the findings of the trial in a clear and transparent manner, following the guidelines for publishing clinical trial results.
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Interpret the results and consider the implications for clinical practice or further research.

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A randomized clinical trial (RCT) is a type of scientific experiment that aims to reduce bias when testing a new treatment. Participants are randomly assigned to different groups to compare the effects of interventions.
Typically, researchers, sponsors, or institutions conducting the trial are required to file documentation regarding the RCT with regulatory bodies.
To fill out an RCT submission, researchers must complete specific forms provided by the regulatory authority, including details about the trial design, participant eligibility, interventions, and statistical analysis plans.
The purpose of an RCT is to evaluate the efficacy and safety of a medical intervention or treatment by comparing outcomes between groups subjected to different treatments.
Key information includes trial design, methodology, eligibility criteria, treatment regimens, endpoints, informed consent processes, and data analysis plans.
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