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METHODS This study was approved by the Institutional Review Boards at each of the two participating institutions (University of California, Davis IRB protocol #488680 and Milwaukee Childrens Hospital
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01
Determine the objectives and goals of the multisite study.
02
Identify the number of sites that will be involved in the study.
03
Develop a clear study protocol that outlines the research design, methodology, and data collection procedures.
04
Obtain ethical approval from relevant institutional review boards for each site involved.
05
Select and train site investigators to ensure consistency in data collection and study procedures.
06
Establish a system for data management and ensure that data is collected uniformly across all sites.
07
Coordinate regular communication and meetings with site investigators to address any issues or concerns.
08
Monitor and evaluate the progress of the multisite study to ensure adherence to the study protocol.
09
Analyze the collected data using appropriate statistical methods and interpret the findings.
10
Prepare a detailed report or manuscript summarizing the study findings and submit it for publication or dissemination.

Who needs a multisite study of?

01
Researchers or organizations conducting large-scale studies that require data collection from multiple sites.
02
Research projects that aim to enhance the generalizability of study findings by including diverse populations or settings.
03
Clinical trials or interventions studies that need a sufficient sample size to ensure statistical power.
04
Studies examining rare diseases or conditions that require collaboration among multiple sites to gather an adequate number of participants.
05
Research projects that aim to validate findings across different geographical locations or cultural contexts.

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A multisite study involves research conducted across multiple locations or institutions to gather comprehensive data and analyze the outcomes of a particular system or phenomenon.
Researchers and institutions conducting multisite studies typically need to file for approvals and reports to ensure compliance with regulatory bodies.
Filling out a multisite study requires detailed documentation about the study protocol, participant selection criteria, data collection methods, and ethical considerations, often involving collaboration between all sites.
The purpose of a multisite study is to enhance the generalizability of research findings by collecting data from diverse populations or settings, allowing for more robust statistical analysis.
Information that must be reported includes study objectives, methodology, participant demographics, site details, data collection procedures, and any adverse events.
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