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Parent Information and Consent Form1. Title of StudyCelecoxib versus placebo as an adjunct to treatmentasusual in children and youth with obsessive compulsive disorder: A single site randomized quadruple
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How to fill out randomized placebo-controlled trial of

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Obtain ethical approval from the appropriate regulatory bodies.
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Define the research question and hypothesis to be tested.
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Randomly assign participants into two groups: one receiving the placebo and one receiving the actual intervention.
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Ensure blinding of participants, researchers, and data analysts to minimize biases.
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Monitor and collect data on outcomes of interest in both groups.
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Analyze the data using appropriate statistical methods to determine the efficacy of the intervention.
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Researchers and scientists who are looking to determine the effectiveness of a new intervention or treatment in a controlled and unbiased manner.
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Randomized placebo-controlled trial is a type of clinical trial in which participants are randomly assigned to either a treatment group receiving the experimental drug or a control group receiving a placebo.
Researchers conducting clinical trials are required to file randomized placebo-controlled trial information.
Researchers must provide detailed information about the trial protocol, study design, participants, interventions, outcomes, and statistical analysis plan.
The purpose of a randomized placebo-controlled trial is to evaluate the efficacy and safety of a new treatment compared to a placebo.
Researchers must report on study design, methodology, results, adverse events, and conclusions.
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