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This form is for submitting research that involves multiple sites to the Institutional Review Board (IRB). It ensures proper coordination and compliance in multi-site research involving human participants.
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How to fill out MULTI-SITE STUDIES

01
Identify the goals and objectives of the multi-site study.
02
Select the sites that will participate in the study based on relevant criteria.
03
Develop a standardized protocol that all sites will follow to ensure consistency.
04
Gather necessary approvals from institutional review boards (IRBs) at each site.
05
Train site personnel on the study protocol and data collection methods.
06
Create a data management plan to ensure data integrity across sites.
07
Regularly monitor data collection and site compliance throughout the study.
08
Analyze data collectively while ensuring to report site-specific findings if necessary.

Who needs MULTI-SITE STUDIES?

01
Researchers conducting extensive studies that require diverse populations.
02
Organizations seeking to generalize results across different geographic locations.
03
Pharmaceutical companies testing drugs across various patient demographics.
04
Public health officials evaluating health interventions in multiple communities.
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People Also Ask about

If a study will be conducted at multiple sites, the IRB-HSR requires a common protocol that is used by all sites. A common protocol is required even if the overall PI is not from UVA. If a common protocol does not exist, templates for a common protocol found on the IRB-HSR Website may be used.
In single case studies, all cases do not have literature reviews but many of them have instead a title like “Case study” or “Case description”. In multiple cases all have a conclusion and the most of them have some sort of literature review but not all of them.
Multiple case study is the intentional analysis of two or more complete single case reports (Stake, 1995). When well-selected and crafted, researchers can use multiple case study to increase external validity and generalizability of their single case study findings (Merriam, 1998).
A multi-site study means that the same research protocol procedures will be conducted at each site. In the past, each study site would submit for and obtain IRB approval from the “local” site IRB. The sIRB policy requires the use of a single IRB to review and approve the research protocol for all of the study sites.
The term MultiSite case studies is often used interchangeably with multiple-case studies, comparative case studies, and what Robert Stake termed “collective case studies.” A MultiSite case study investigates a defined, contemporary phenomenon that is common to two or more real-world or naturalistic settings.
A multi-site clinical trial involves the implementation of the same clinical protocol at two or more independent investigational sites where participants are seen for an intervention and/or outcomes assessment.
The term MultiSite case studies is often used interchangeably with multiple-case studies, comparative case studies, and what Robert Stake termed “collective case studies.” A MultiSite case study investigates a defined, contemporary phenomenon that is common to two or more real-world or naturalistic settings.
A multisite study provides investigators with the opportunity to research different programs using a shared study design and methodology. Different sites investigate different services or programs, but have a common protocol.

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Multi-site studies refer to research projects conducted at multiple locations or sites, allowing researchers to gather diverse data and enhance the generalizability of their findings.
Researchers and institutions conducting studies that span multiple geographic locations are typically required to file multi-site studies, particularly when the research involves human subjects.
To fill out multi-site studies, researchers should provide comprehensive details about each site, including study protocols, participant recruitment strategies, site-specific approvals, and data management practices.
The purpose of multi-site studies is to gather more extensive and varied data, improve statistical power, address research questions that span diverse populations, and improve the reliability and validity of study results.
Information that must be reported includes the number of sites participating, site characteristics, overall study design, specific roles of each site, consent procedures, and data collection methods.
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