OnCore: DFD - Multi-site Trial

Data Field definition table including the field name, definition, entry instructions and requirements
Field Name Definition Requirement
Entry Instructions
Responsible for Entry QA
Multi-site Trial Multi-site Trial can be used to indicate that the study is enrolling subjects at multiple sites (i.e. more than one university or research organization).

Required

Oncology:

No: limited to participating institutions in the Cancer Center's CTRP family (UW, 1SP, VA, Johnson Creek, Prohealth, UWH Northern Illinois/Swedish American)

Yes: includes participating institutions other than those listed above (e.g, MCW/Froedert, Marshfield Clinic, national cooperative group sites not listed in OnCore), regardless of which sites are listed in the PC Console > Institutions tab.

Non-oncology:

If there are two or more institutions participating in the study, regardless if they are listed in the PC Console > Institutions tab, then multi-site trial should be checked 'Yes'.

Note: For studies open to affiliates only (OAO) that have one participating institution and the UW performs regulatory functions, 'No' should be selected because the UW is not considered a participating site. For lab studies where subject are consented and samples are collected at an outside institution, but the sample analysis is being performed at UW, 'Yes' should be selected because both institutions are participating in the research.

PC Console edit / (Affiliate) Protocol Coordinator

Yes

NCI Report field



KeywordsMulti-site Trial   Doc ID29232
OwnerMolly H.GroupSMPH Research Informatics
Created2013-03-26 10:41:27Updated2024-01-31 14:05:20
SitesInstitute for Clinical and Translational Research, SMPH Research Informatics
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