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Official Title of the study: Randomized Controlled Trial of Web Based Tools to Improve Medication Continuity in Adolescents With ADHD NCT number: NCT04386096 Document name: Informed Consent Form Date
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Define the research question or hypothesis that will be tested in the RCT.
02
Determine the study population and eligibility criteria.
03
Randomly assign participants to intervention and control groups.
04
Implement the intervention and control conditions according to the study protocol.
05
Collect data on the outcomes of interest at predefined time points.
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Analyze the data using appropriate statistical methods.
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Interpret the results and draw conclusions about the effectiveness of the intervention.

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Randomized controlled trial overview design is a type of study design where participants are randomly assigned to different groups to receive different interventions or treatments, to evaluate the effectiveness of the intervention.
Researchers, scientists, or institutions conducting clinical trials are required to file randomized controlled trial overview design.
Randomized controlled trial overview design should be filled out with detailed information about the study design, participant selection criteria, interventions, outcomes, and statistical analysis plan.
The purpose of randomized controlled trial overview design is to minimize bias and confounding factors, and to assess the effectiveness of interventions or treatments in a systematic and rigorous manner.
Information such as study objectives, participant eligibility criteria, intervention details, outcome measures, statistical analysis plan, and ethical considerations must be reported on randomized controlled trial overview design.
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