Useful resources developed by the CCB members, for both new cohorts embarking on data collection and established cohorts interested in collaboration with an introduction of the Central Data Repository and the eCRF.
The Central Data Repository (CDR) is COMING SOON!
When ready the link to the CDR will appear at the bottom of this page.
The CDR is a publicly accessible online database of clinical research studies targeting infectious diseases with epidemic and pandemic potential in Europe. The CDR will be updated regularly to include new studies according to new global threat and European epidemiological scenario.
Why was the CDR developed?
The CDR was developed as part of the EU-funded VERDI (GA-101045989) and CoMeCT (GA-101136531) projects to facilitate data sharing, foster collaboration, and prevent duplication in clinical research efforts. It offers key stakeholders and researchers an overview of recently closed (within three years) and ongoing randomised clinical trials (RCTs) and cohort studies (CS) on emerging threats or public health emergencies of international concern, to support rapid identification and activation of infrastructures and/or clinical sites study activation as well as to facilitate linking of relevant initiatives and networks and support coordination initiatives of European research.
What clinical research studies are included in the CDR?
The CDR includes CSs, RCTs and adaptive platform trials, carried out in Europe that focus on infectious diseases, particularly those that may be considered emerging threats. Currently, the CDR includes studies that analyse SARS-CoV-2 acute infection (treatment), post-COVID-19 syndrome (treatment), mpox (natural history, treatment, and vaccination), and avian influenza A (H5N1) (treatment and vaccination); and adaptive platform trial infrastructures.
After filtering or searching for relevant conditions or keywords, the user receives a list of clinical studies. Each study is named after the cohort title, or if unavailable, the principal investigator of the study.
What information can be found in the CDR?
The CDR consists of three parts: interactive filters, a map of Europe showing the number of studies per country, and a browsable list of the studies. The map and the study list show the studies according to the selected filters. Each study in the CDR is detailed in a Study Identity Card, which includes the study’s name, design, number of participants, enrolment dates, location, population, setting, pathogen, disease, and biobanked samples.
How is information collected for the CDR?
Studies are identified across several publicly available sources (PubMed, Scopus, ECRIN, ClinicalTrials.gov), and through direct contact with the Cohort Coordination Board members, the VERDI and COMECT scientific networks, and other relevant researchers. The screening of the studies is carried out applying an artificial intelligence (AI)-supported tool supervised by infectious diseases specialists. Study metadata is provided by principal investigators and/or extracted from publicly available sources, employing a number of automated and semi-automated methods. The studies are all assigned applicable highly curated descriptors,enabling rapid and accurate browsing.
Future developments
Terms and conditions
The CDR is a platform constructed to provide an overview of the studies running in Europe. While the data is provided in good faith and to the best of our knowledge, neither UNIVR nor any VERDI/COMECT partners make any warranty, express or implied, including warranties of fitness for a particular purpose, or assume any legal liability or responsibility for the accuracy, completeness, or usefulness of any information provided (either isolated or in the aggregate), or represents that its use would not infringe privately owned rights.
The data is intended for Educational and Research purposes only. The term Educational Purposes means* (i) in the case of a Qualified Educational Institution, Faculty or Other Authorized Educational Licensees, purposes directly related to learning, teaching, and training, that are part of the instructional functions performed by a Qualified Educational Institution or Other Authorized Educational Licensee and (ii) in the case of an individual, purposes related to learning and training. “Educational Purposes” does not include research, commercial, professional, or any other for-profit purposes.
Get in touch
We are actively looking to collaborate with other initiatives working in this area, and we welcome you to contact us if you are interested in collaborating, including or amending data onto the CDR.
Within the EU-funded VERDI project, the CCB has been developing a core dataset of variables to be collected for MPX and STI cohorts. Similarly, a core set of variables will be provided also for all IDs with epidemic or pandemic potential, as defined within the CoMeCT project. This will allow researchers from all over the world to use standardised items when investigating specific ID conditions, with the overarching result of providing clearer, more reliable results. Included in this work is the elaboration of an eCRF, that will be publicly available and downloadable as an Excel file.
We are actively looking to collaborate with other initiatives working in this area, and we welcome you to contact us if you are interested in collaboration.
