Table 1.
Study feasibility assessment criteria
| Study element | Importance for feasibility assessment | 
|---|---|
| Study and/or protocol synopsis | Sufficient detail is necessary to determine the research activity sites are likely to perform, and what resources and qualified personnel are needed | 
| Site budget | Draft budgets are acceptable, but sufficient detail must be included to indicate research expenses at the sites will be covered | 
| Research question, impact, and importance of the study | Studies must align with clinical priorities at network sites | 
| Cohort phenotype, total number of patients, and expected recruitment rate | Inclusion and exclusion criteria, ICD-10 codes, or other descriptions are necessary to determine if sites have sufficient patients and whether recruitment can be accomplished | 
| Deadlines for submission of study documentation | Data analysts, providers, and other clinical personnel need sufficient time to complete activities preparatory to research (e.g., electronic health record data extrapolation, completion of site surveys) | 
| Likelihood of site selection | Time to provide study feedback and documentation is not funded, so sites must justify this investment and have a reasonable likelihood of being selected for a study | 
| Likelihood of funding | Sites with limited capacity for research are not typically resourced to absorb costs associated with unfunded studies, so priority is given to studies with or having a higher likelihood of funding (e.g., grants that have received fundable scores) | 
| The “Ask”- what does the principal investigator need from prospective sites | List of required items from sites (e.g., protocol feedback, letter of support, site survey, subcontract materials) | 
ICD-10, International Classification of Diseases, 10th revision.