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Randomized Trial of KEEP, a Preventive Intervention for Foster Preschoolers (KEEP) NCT03106636 June 2, 2020Table of Contents 1. STATISTICAL ANALYSIS PLAN APPROVAL SIGNATURES .................................................................1

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Step 1: Start by gathering all the necessary information for the trial, such as the study protocol, randomization process, and data collection forms.

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Step 3: Ensure that all participants meet the inclusion criteria and obtain their informed consent before proceeding with the trial.

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Step 4: Randomize the participants into different groups using a predetermined randomization process to ensure unbiased allocation.

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Step 5: Follow the intervention and control protocols as outlined in the study protocol for the trial.

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Step 6: Collect data on the outcomes of interest using standardized data collection forms and ensure proper documentation.

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Randomized trial of keep-p is a clinical study design in which participants are randomly assigned to receive either the intervention being studied or a comparison intervention.

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Researchers conducting clinical trials are required to file randomized trial of keep-p with the appropriate regulatory authorities.

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Randomized trial of keep-p can be filled out by providing detailed information about the study design, participant recruitment criteria, intervention details, and data analysis plan.

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The purpose of randomized trial of keep-p is to evaluate the efficacy and safety of a new intervention by comparing it to an existing standard of care.

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Information such as study objectives, design, methodology, participant eligibility criteria, treatment plan, and statistical analysis plan must be reported on randomized trial of keep-p.

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