Clinical trial site identification practices and the use of electronic health records in feasibility evaluations: An interview study in the Nordic countries

Niina Laaksonen, Mia Bengtström, Anna Axelin, Juuso Blomster, Mika Scheinin, Risto Huupponen

Research output: Contribution to journalArticleScientificpeer-review

Abstract

Introduction:Feasibility evaluations are performed to create the best possible starting point for the set-up and execution of a clinical trial, and to identify any obstacles for successful trial conduct. New digital technologies can provide various types of data for use in feasibility evaluations. There is a need to identify and compare such data sources for trial site identification and for evaluating the sites? patient recruitment potential. Especially, information is needed on the use of electronic health records. We investigated how different data sources are used by pharmaceutical companies operating in the Nordic countries for identifying trial sites and for evaluating their potential to recruit trial participants.Methods:This was a semi-structured qualitative interview study with 21 participants from pharmaceutical companies and contract research organizations operating in Finland, Sweden, Denmark and Norway. Qualitative content analysis was applied.Results:For identifying countries and trial sites on a global level, the trial sponsors mostly used databases on previous trial performance. The use of electronic health record data was very limited. Sites? and investigators? visibility in various databases was seen as fundamental for their countries becoming selected into new clinical trials. For estimating the sites? recruitment projections, most sites were seen to base their patient count estimates solely on their previous experience. Some sites had reviewed their electronic health record data, which was considered to increase the accuracy of their recruitment estimates and these sites? attractivity. Along with dialogs with investigators, the sponsors used various data sources to validate the investigators? estimates. Legislative obstacles were seen to hinder the use of electronic health record queries for estimation of patient counts.Conclusion:Visibility in the databases used by trial sponsors is crucial for the countries and sites to be identified. Site selection appears to be based on trust and relationships built from experience, but electronic data provide the support upon which the trust is based. Estimation of the number of potential trial participants is a complex and time-consuming process for both investigators and sponsors. Sponsors seem to favour sites who could support their patient count estimates with electronic health record data as they were quicker in providing the estimates and more reliable than sites with no electronic health record evidence. The patient count evaluation process could be simplified, accelerated and made more reliable with more systematic use of electronic health record evidence in the feasibility evaluation phase. This would increase the accuracy of the patient count estimates and, on its part, contribute to improved recruitment success.
Original languageEnglish
Pages (from-to)724-731
Number of pages8
JournalClinical Trials
Volume18
Issue number6
DOIs
Publication statusPublished - 2021
MoE publication typeA1 Journal article-refereed

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