key: cord-0965806-l3sviguv
authors: Helmer, Tara T; Lewis, Adam A; McEver, Mark; Delacqua, Francesco; Pastern, Cindy L; Kennedy, Nan; Edwards, Terri L; Woodward, Beverly O; Harris, Paul A
title: Creating and Implementing a COVID-19 Recruitment Data Mart
date: 2021-03-30
journal: J Biomed Inform
DOI: 10.1016/j.jbi.2021.103765
sha: 18d7071f33911a79e7ad2b4e0523080eb022bfff
doc_id: 965806
cord_uid: l3sviguv

The COVID-19 pandemic has resulted in an unprecedented strain on every aspect of the healthcare system, and clinical research is no exception. Researchers are working against the clock to ramp up research studies addressing every angle of COVID-19 – gaining a better understanding of person-to-person transmission, improving methods for diagnosis, and developing therapies to treat infection and vaccines to prevent it. The impact of the virus on research efforts is not limited to investigators and their teams. Potential participants also face unparalleled opportunities and requests to participate in research, which can result in a significant amount of participant fatigue. The Vanderbilt Institute for Clinical and Translational Research recognized early in the pandemic that a solution to assist researchers in the rapid identification of potential participants was critical, and thus developed the COVID-19 Recruitment Data Mart. This solution does not rest solely on technology; the addition of experienced project managers to support researchers and facilitate collaboration was essential. Since the platform and study support tools were launched on July 20, 2020, four studies have been onboarded and a total of 1693 potential participant matches have been shared. Each of these patients had agreed in advance to direct contact for COVID-19 research and had been matched to study-specific inclusion/exclusion criteria. Our innovative Data Mart system is scalable and looks promising as a generalizable solution for simultaneously recommending individuals from a pool of patients against a pool of time-sensitive trial opportunities.

The COVID-19 pandemic has proven highly disruptive in the planning and implementation of biomedical research. 1, 2 The unforeseen logistical difficulties that have plagued clinicians during this crisis, such as shifts in staff responsibilities, the need for physical distancing, and shortages of personal protective equipment, 2, 3 have also extended to researchers planning and conducting COVID-19 related trials.

Furthermore, investigators studying COVID-19 have faced additional challenges unique to this area of research, due at least in part to the inherent urgency to quickly discover safe and effective measures to test, treat, and prevent the disease, often while attempting to balance and continue their pre-COVID-19 research priorities and responsibilities.

First identified in December 2019, 4 COVID-19 has been poorly characterized, 5,6 lacking standardized codes for testing and diagnosis prior to March 2020. 7 Initial research favored single-arm or observational studies over randomized clinical trials, 8, 9 and the rush to publish results led to questionable ethical choices in research methods 8, 10 and in some cases retracted manuscripts. 11 As research ramped up, a flood of trials began entering the pipeline with initial funding from institutional sources or grant supplements, then giving way to larger dedicated coordinated trials. Over the next several months, the National Institutes of Health (NIH) responded to the crisis by re-appropriating at least two well- Academic medical centers were faced with unprecedented competing demands on their research ecosystems. Healthcare IT teams, already overtaxed to support increased COVID-19 clinical informatics needs, were called in to assist with pressing requests from the research enterprise. 12 In addition, data emerging early in the pandemic on racial and ethnic disparities in COVID-19 infection rates and outcomes 13 underscored a critical need to find ways to support enrollment of underrepresented minority participants in COVID-19 clinical trials. 14 The observed growth of COVID-19 submissions to ClinicalTrials.gov and to our own internal IRB system suggested to our team at Vanderbilt University Medical Center (VUMC) that we would ultimately face the problem of multiple studies simultaneously recruiting from the same participant pool. 15 This presented additional complexities, as research teams had historically recruited and worked in a somewhat isolated fashion without the need to co-coordinate or "share" a population of eligible research patients. Initially, our process at VUMC involved having attending physicians form 'morning huddles' to guide inpatient prioritization for consideration and assignment to specific recruiting studies.

Outpatients, however, not being centrally located, posed a new problem--how to optimize participantto-trial matching for a population not amenable to our internal workflow. Furthermore, the need to identify potential research participants within hours of their COVID-19 diagnosis presented a unique challenge to researchers testing outpatient treatments and highlighted a critical need to partner with biomedical informatics specialists in order to leverage all available systems to fight the pandemic. We needed to formulate a more efficient system that would ensure outpatients also had an opportunity to participate in important, targeted COVID-19 research projects.

As an academic medical institution, VUMC has long embraced a goal to ensure that every patient has an opportunity to participate in clinical research. Coupling this aspiration with the desire to support as many competing COVID-19 trials as possible, we compiled a team from the VUMC research enterprise that included informaticians, research support experts, compliance professionals, and research operations key informants. Together, we designed and built a Data Mart for COVID-19 research recruitment with the goal of identifying the 'right patient at the right time for the right COVID-19 study'. This Data Mart platform leverages REDCap (Research Electronic Data Capture) 16, 17 and is supported by a combination of data feeds (including Fast Healthcare Interoperability Resources [FHIR] 18 endpoints) from our Epic electronic health record (EHR) system. The Data Mart application aggregates this information along with patient 'consent to contact' (C2C) permissions collected from operational Data Mart workflow, then automatically generates participant 'goodness of fit' assessments for a pool of actively recruiting trials. The Data Mart also utilizes a 'virtual huddle' model to support the sharing of potential matches across studies. While originally formulated to allocate participants to outpatient trials, our method is suitable for inpatient trials as well. Here we describe our Data Mart platform and early results of implementation, along with a set of generalizable 'lessons learned' that may prove beneficial to other teams faced with similar recruitment and logistical challenges.

The design, development, and deployment of a recruitment-oriented Data Mart platform required input and support from VUMC policy teams, health equity experts, Human Subjects Protection experts, and Privacy Office leadership. Overall Data Mart leadership, technical programming, project management, and research stakeholder engagement efforts were provided by the Vanderbilt Institute for Clinical and Translational Research (VICTR). The platform was developed in an iterative fashion, evolving over time to support needs articulated by the research community most engaged with ongoing or projected COVID-19 trials. Details about the technical platform, data sourcing, and end-user process design details are provided below.

In designing the Data Mart platform, we considered three essential goals: 1) evaluate every patient testing positive for COVID-19 for consideration as a candidate for one or more trials; 2) democratize access to the Data Mart matching service for as many research studies as possible; and 3) respect VUMC's 'opt-in' policy, which allows patients to choose whether or not to be contacted directly for research studies outside of normal clinical provider encounters.

Given resource constraints and a design requirement to ensure the system could rapidly evolve over time, we chose REDCap 16 as our central platform for data aggregation, management, and reporting workflow. REDCap is a secure web application developed and disseminated by our VUMC team and is available at no cost to academic, non-profit, and government organizations around the world. 17 Whenever possible, we used native functionality within the REDCap system to support Data Mart data collection and workflow. In cases where Data Mart data integration or complex workflow requirements were not feasible with standard REDCap functionality, we developed REDCap External

Modules. External Modules are add-on software programs that extend REDCap's current functionality or allow customizations and enhancements for REDCap's existing behavior and appearance. Software developers use GitHub for hosting, with externalization to the global REDCap community through a common dissemination repository. 19

For clinical data sourcing, we prioritized use of Epic HL7-FHIR endpoints whenever available, supplementing with information from a centralized VUMC Health Data Repository (HDR) 20 and Research Data Warehouse (RDW) 21 as needed. The HDR was especially useful at the beginning of the pandemic when COVID-19 lab results were not readily available from Epic. Later, we reworked our pipeline to retrieve results directly from Epic, but we still use the HDR as a means of identifying tested patients before results are completed and available. Evaluation of numerous study protocol inclusion requirements for time-to-enrollment after COVID-19 testing and diagnosis highlighted a need to expedite the opt-in mechanism. Many outpatient treatment trials would require patients to begin treatment within days of testing positive for COVID-19, so the system needed to support a workflow in which patients had the opportunity to consent to contact before their diagnosis was confirmed. Starting a "Consent to Contact' (C2C) permission request after diagnosis would require too much calendar time, thereby eliminating a high number of patients from consideration for COVID-19 trials. Given this, we decided to initiate the process as upstream as possible by sending the C2C message to patients immediately after they were tested (with event triggered by clinical system notification of a COVID-19 test), rather than waiting for confirmed results from laboratory systems. Shifting the time for messaging allows patients not only to share their preference for contact about COVID-19 research, but it also introduces them to the idea of COVID-19 research earlier. Finally, it also allows researchers to contact them within hours of the confirmed positive test result.

To facilitate the C2C workflow, we used an application programming interface (API) data feed from the VUMC HDR to detect when a new test was recorded within the EHR. Upon receipt, a medical record number (MRN) is inserted in a special 'C2C' REDCap project designed to immediately and automatically pull basic demographic contact information (patient name, e-mail address, contact phone number, and preferred language) via HL7 FHIR endpoints. REDCap then prepares and sends to all outpatients an automated message to the patient from Vanderbilt's Executive Vice President for Research. The default C2C message is created as an email, in English or Spanish depending on the patient's known preferred language as collected in the EHR. If an email address is not available in the EHR but a mobile number exists, the C2C database sends an SMS message. Every message includes contextual information and a link to a one-question survey, available in English or Spanish, asking the patient if they would like to be contacted directly for COVID-19 research opportunities at Vanderbilt. Responses are recorded in the C2C

To complement the C2C project, REDCap 'listens' to another VUMC HDR data feed for real-time detection of any new positive lab test result for COVID-19. When detected, the patient's MRN is registered in a second database (Data Mart). FHIR and non-FHIR data sources are then used to automatically extract demographics, laboratory results, vitals, medications, allergies, problem list, and inpatient/outpatient status from the EHR for immediate deposit in the Data Mart. Specifically, data are extracted that are relevant to known inclusion and exclusion criteria for Data Mart supported projects. Finally, the Data Mart program automatically refreshes each known COVID-19 positive patient with an 'OK to Contact' flag, collecting this information from the aforementioned C2C database. This repeating check ensures individuals who test positive before consenting to contact are included as soon as they consent, and also allows a mechanism to reset a patient's status if they change their mind later (either way) about being contacted.

For each participating trial, we code key inclusion/exclusion criteria rules to run against EHR-derived data for every potential participant who has agreed to direct contact. These criteria are informed by the study protocol with input from the PI/study team and driven by what is computable using retrievable EHR data. The computable phenotype coding work is performed in a REDCap External Module using a modular approach, which allows rapid deployment or sunsetting of individual COVID-19 studies. VICTR Research Support Services (RSS) team members use a dashboard in the REDCap system to view 'just-intime' recommendations for suitability of each patient eligible to participate in each supported trial. The dashboard snapshot view quickly and easily provides the following information: study short name, the total number of current potential matches for that study, which patients have already been shared with the study team (indicated by an envelope icon), which patients have not yet been shared (indicated by a check mark), and a '?' icon that links out to view study specific logic. 

The process for onboarding a new project requires multiple steps ( Figure 3 ) and is initiated with a REDCap intake form to capture pertinent study information. Upon receipt, the request is reviewed for completeness and appropriateness. VICTR RSS reviews the study-specific inclusion/exclusion criteria to determine compatibility with available data fields in the Data Mart. During an iterative process, VICTR RSS works with the PI/study team to finalize the criteria to drive the Data Mart logic. The goal is to provide the study teams with a report that gets them close to their target population, with the understanding that additional screening in the EHR will be necessary before a potential participant is deemed eligible and contacted.

In addition to the study-specific eligibility criteria, additional standard logic is included for every study, for example, to include patients who agreed to direct contact and to exclude all inpatients. With the logic finalized, the study specific external module is added to the Data Mart and appropriate IRB approval is confirmed. We also developed standardized template language to describe the Data Mart, which research teams can use for IRB submissions.

For any competing trials, the respective PIs/study teams are required to meet with VICTR RSS in a 'virtual huddle' to discuss equitable distribution of potential matches across studies before potential matches are shared. In that huddle a schedule is developed for sharing patients equitably across each of the competing trials. Currently a 2-day rotating schedule is in place. Each day a single study is designated as primary and gets right of first refusal; the other study is designated as secondary. The list of potential matches is sent to the primary study in the early morning. The primary study is expected to screen these patients and indicate their enrollment status in Epic -for example, Identified, Interested, Ineligible, Declined, On Study. The list of potential matches, including any overlapping patients, is then sent to the secondary study around mid-day. The secondary study team will initially check for any existing enrollment statuses in eStar. If a patient is designated as Identified, Interested or On Study they will not continue to screen nor will they try to contact the patient. This is critical to minimize participant fatigue and participant confusion. If a secondary study checks that patient later and sees an enrollment status of Ineligible or Declined, they can proceed with additional screening and if applicable, contact the patient. The use of enrollment statuses is critical in promoting transparency across studies and minimizing participant fatigue.

Once the study has been added to the Data Mart and the expectations have been outlined and agreed to by the study teams, the 2-step process for identifying and sharing potential matches can begin. VICTR RSS reviews the dashboard for each record flagged with a check icon and marks each of those individual records to indicate the patient has been identified as a potential match for the respective study. This results in the check icon being updated to an envelope to indicate the patient has been sent to the study team. Next, VICTR RSS clicks on a button within the Outpatient Study Dashboard to export an excel file containing all the current matches for the respective study. The file, which contains patient MRN, name, date of birth, email address, phone number and date of last COVID positive test, is sent to the study team in a secure manner. For all subsequent reports, one additional step involves VITCR RSS removing any patients marked as 'Sent to Study' from the exported file before sharing it with the study team. In total, VICTR RSS spends about 20 minutes a day reviewing the dashboard, generating reports, and sharing the reports with the study teams.

After the daily report of potential matches is sent, eligible patient lists are forwarded, the workflow shifts from VICTR RSS and the Data Mart platform to the study team. Once the study team receives its list of potential matches in the morning, they conduct additional screening via an electronic chart review in Epic to confirm study eligibility. One key aspect of their chart review is to confirm if the patient has any known current or recent research contact or enrollment activity. This review is crucial to help minimize participant fatigue. For example, if a research team is screening for an interventional trial and they confirm the patient is already on an interventional trial, they would not proceed as that would be a known reason for exclusion.

Administrative support is crucial to facilitate operational workflow.

We launched participant C2C operations on May 1, 2020. In the first 5 months of operation (5/1/2020 -10/9/2020), testing awareness generated automated messages to 62,427 individuals who were tested at the main hospital or one of 22 VUMC Testing Centers. The vast majority of these messages were English version emails (see Table 1 ). We report in Table 2 early results for generating study specific potential matches and enrollment outcome metrics from each of these four studies. There are many confounding factors that determine final eligibility and willingness to participate and enroll in specific studies. An examination of these factors is beyond the scope of this report, so we are reporting here only high-level enrollment statuses based on researcher reporting screening logs. We report two columns for enrollment (Data Mart attribution + total enrollment) to illustrate that the Data Mart is complementary with other methods of recruitment. Ongoing studies are also pursuing enrollment via clinician referrals, participant-facing printed recruitment materials, and other methods. 

We asked research teams to provide qualitative feedback on the utility of the Data Mart, recognizing that the positive utility might be measured in at least two ways: 1) increasing the rate of recruitment;

and/or 2) reducing the amount of work needed to support recruitment. Qualitative feedback provided from research teams focused mainly on time saved, both in identification and screening of potential participants. The C2C workflow saves significant time by eliminating the need to go through a patient's healthcare provider to approach them about a potential research opportunity. Additionally, the algorithm-based narrowing of the COVID-19 population by study-specific eligibility criteria saves research coordinator time by reducing the volume of needed chart reviews.

One research nurse summed it up nicely, "The Data Mart has saved us hours in this process by filtering for many of our exclusions on the front end and highlighting the patients who are more willing to participate in research." Another stated, "The fact that we have 6 individuals on our radar who are eligible at this very moment is significant (aka amazing) -there is no way we would have been able to identify these 6 people quickly enough had we been tasked with reviewing all the charts of people who tested positive."

In addition to the study-specific results, the ability to provide equitable access combined with rapid deployment of new studies from both administrative and technical perspectives was crucial to our evaluation of the Data Mart. The administrative process -from study intake, to review, to finalizing eligibility criteria and communicating those to the software developers -has been streamlined using requires approximately ten minutes of programmer time. While we have considered building a selfservice researcher-oriented interactive query interface, we are not convinced the added efficiency gain would be worth the additional investment in programming and training resources for this project.

The Data Mart fosters a partnership between VICTR RSS and each COVID-19 study team.

Serendipitously, we have seen that the model also promotes coordination and collaboration among the study teams. Continual, joint monitoring and communication ensures that the right patients are being identified by the pre-defined criteria, or whether adjustments are needed. Once competing studies have been onboarded, study teams meet in a 'virtual huddle' with VICTR RSS to agree on an equitable allocation of potential participants. By working together on the front-end, research teams have learned about one another's trials, which has allowed them to refer patients to one another and to introduce other research options or differentiate their study when discussing research with patients.

Transparency is a critical component of our process and is primarily facilitated by the tracking of patient enrollment status in Epic. A participant who enrolls in an interventional trial is marked accordingly in Epic, and is not invited to join another interventional trial, thus helping to mitigate participant fatigue.

Similarly, tracking enrollment status in Epic allows research teams to determine whether the patient has previously been contacted or declined consent for another study, which are important details to acknowledge when contacting the patient about a subsequent research opportunity.

While facilitating screening and recruitment for COVID research was our primary goal, developing a system to support inclusion among underrepresented minorities was essential. We designed our process so that the original C2C message would be delivered in either English or Spanish, depending on the preferred language noted in a patient's EHR. Also, noting that Blacks and Hispanics are roughly twice as likely as whites (23% and 25% vs. 12%) to rely on smartphones for internet access, 23 and are more likely than whites to use a smartphone to access health information, 24 we built our C2C project to support SMS messaging in addition to email. We are currently exploring additional languages for the C2C invitation and estimate we will be supporting Arabic in the near future.

Although originally designed to help researchers, our Data Mart also benefits patients, particularly those who may be emotionally overwhelmed at the time of diagnosis or too sick to make a confident choice among multiple studies. An invitation to participate in a COVID-19 clinical trial, delivered soon after a positive test, may provide a message of hope to the patient and family in a difficult time. The C2C message is likely the first trial-related communication received by potential participants, and thus we strived to make it welcoming, informative, clear, and action oriented. We have revised it since the initial launch based on feedback from patients, our Privacy Office, and our Patient Education Department.

We are hearing from research teams that computable phenotypes and patient-trial matching algorithms are saving time for research coordinators over traditional chart review processes. This indirectly supports patient privacy because the computable matching process reduces the number of chart reviews that would otherwise be needed to filter eligible patients.

The Data Mart has proven successful and valuable for recruitment of COVID-19 trial participants, but we recognize there is no single perfect solution to identification of participants for all clinical trials. We have several other systems in place at VUMC, including native Epic research tools, ResearchMatch, 25 TrialsToday, 26 and SubjectLocator. 21 (testing) may be higher than we would see in a more general request framework. Our computable approach to matching a pool of patients to a pool of potential trials also ensures a high level of flexibility and customization with minimal IT investment on a per-study basis.

Our current participant eligibility distribution workflow is dependent on RSS personnel to serve as the honest broker and share daily matching reports with each respective study. This requires someone to log into the Data Mart, mark each new 'match' for the respective study, export the matching report and

share it with the respective study team in a secure manner. While the level of effort at this point is minimal (20 minutes per day in serving four concurrent trials), eliminating this 'honest broker' dependency would make the model even more scalable. We consciously made the decision to implement our facilitated honest broker model over a purely self-service researcher workflow for expediency. We are learning lessons in our current work with COVID-19 research teams that will be helpful in making design decisions should we decide to later build a fully automated system.

The concepts and lessons learned from developing and implementing our Data Mart platform should be transferrable and valuable to others designing or considering adoption of similar systems.

1) Transparency, trust, and teamwork are foundational requirements for leading-edge innovation projects like this one. Multiple concept discussions were needed with regulatory and compliance leaders before considering launch. Our culture at VUMC favors innovation and is based on many years of cross-team collaboration. Given this high level of trust, institutional leaders are willing to support multiple iterations of concept clearance when needed. The patient messaging for our 'consent to contact' language is a great example and has gone through several iterations and review cycles from the Privacy Office, Office of Research, and Patient Education.

2) Technical architecture and tools are important, but they comprise only a part of the process and its success. Administrative support is crucial, as is the willingness of study teams to collaborate and be as transparent as possible about their outreach to potential matches and the subsequent outcome.

3) In an evolving pandemic, perfect is the enemy of good and there is no way to confidently define longterm system requirements and specifications. We focused all energy on solving a perceived (and later confirmed) need, then allowed our methods to evolve over time. In some cases, a short-cycle sprint of work highlighted errors in assumptions or unexpected dependencies, so we were forced to backtrack after gaining more information from one or multiple stakeholders. In all cases, we considered the platform to be an evolving solution and our choice of REDCap as an architectural platform allowed very rapid technical prototypes that were easy to evolve or rebuild.

4) Lower-tech solutions are often very useful when timing is critical, and assumptions are untested. An example of how this strategy worked in practice was our 'honest broker' huddle process. We could have spent months perfecting it, only to realize our assumptions were incorrect. Instead, by instituting the huddle early on, we were able to make it a work-in-progress and improve upon it as we gained insight from actual discussions on patient allocation. Another low-tech example involves our methods for evaluation of participant enrollment after Data Mart recommendations are made. We may eventually build a participant attribution workflow module into the Data Mart, but coordinators have been very receptive to using their existing screen logs to supply evaluation metrics whenever requested.

5) It is constructive to explore and recognize multiple ways to evaluate success. In our early assessment exercises, we recognized that success could be measured by increasing the rate of enrollment for trials and also by reducing the time required by study personnel to evaluate patients for enrollment. Our approach minimizes the need for study teams to forage through medical records and reduces 'coldcalling' by study teams. Given upfront C2C workflow, fewer calls are needed to enroll the same number of participants and this gain in efficiency has been cited by research teams to be as important as the effective rate of recruitment. We also reduced the need for study teams to go through the provider to gain the patient's permission for research contact. This is especially critical during a pandemic when demands on clinicians' time are already excessive.

6) Focusing on a specific problem while also considering generalizability for future use cases is advantageous. There is nothing particularly unique about COVID-19 in our approach to building the Data Mart system and we are already thinking about future ways to abstract concepts and technical tools for other recruitment and enrollment workflow solutions.

The REDCap-based Data Mart is operational and yielding beneficial results for the VUMC research enterprise. We will continue to learn and grow the system as we onboard each new study, but the overall framework is working well and equitably serving both patients and researchers in the conduct of research during the current pandemic. While the details of our approach are somewhat unique to VUMC systems, the overall methods and lessons learned should be transferable. This lightweight technology approach is not unique to the COVID-19 recruitment space and we believe it could be customized for use in other biomedical research domains where multiple trials should be considered for each patient (e.g., diabetes clinic, movement disorders clinic). In Appendix C, we provide details on data sources, logistics, and reporting as guidance for other institutions considering a similar implementation.

We are happy to share our model, REDCap project dictionaries, and External Modules with others and plan to do so through webinars and other dissemination channels.

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Subject: Learning more about COVID-19 research Hello [first_name],

As you know, COVID-19 has led to a public health crisis. In just a couple of months, the pandemic has made a deep and lasting impact on our patients, our community, our state, our country, and our world.

We need your help-now more than ever. By learning about the COVID-19 research we're doing at Vanderbilt, you can help us win the fight against this pandemic.

As our colleagues in our hospitals and clinics provide the best care possible to all our patients affected by COVID-19, our research community is joining them in the fight. Together with some of the country's top experts in clinical care, infectious diseases, and emergency planning, our world-renowned researchers are focusing on finding ways to:

 best treat all patients who are sick with COVID-19,

Impact of the COVID-19 pandemic on clinical research

COVID-19 and readjusting clinical trials. The Lancet

Safely conducting essential research in the face of COVID-19

First cases of coronavirus disease 2019 (COVID-19) in the WHO European Region

Presenting Characteristics, Comorbidities, and Outcomes Among 5700 Patients Hospitalized With COVID-19 in the New York City Area

Symptom Profiles of a Convenience Sample of Patients with COVID-19 -United States

Announcement-New-ICD-code-for-coronavirus-3-18-2020.pdf. Accessed

Biomedical Research in Times of Emergency: Lessons From History

COVID-19, equipoise and observational studies: a reminder of forgotten issues

Ethical challenges in the COVID-19 research context: a toolkit for supporting analysis and resolution

Retracted COVID-19 articles: a side-effect of the hot race to publication

Ideas for how informaticians can get involved with COVID-19 research

Racial Health Disparities and Covid-19 -Caution and Context

Racial Disproportionality in Covid Clinical Trials

Coronavirus Researchers Compete to Enroll Subjects for Vaccine Tests

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support

The REDCap consortium: Building an international community of software platform partners

When customizing an EHR, don't get "hyper-focused on the tech

Secondary use of clinical data: The Vanderbilt approach

What is Operation Warp Speed?" | NIH: National Institute of Allergy and Infectious Diseases

Demographics of Internet and Home Broadband Usage in the United States

Racial and ethnic differences in how people use mobile technology. Pew Research Center

Trial Sites Around the Nation Report Great Interest in Volunteering for COVID-19 Vaccine Trials

Thousands Volunteer for COVID-19 Vaccine Study

The authors would like to thank Rob Taylor for assisting with REDCap integration and validation, Chad Lightner for designing figures for the paper, and Lori Anne Parker-Danley for reviewing and revising the patient messages. 

☒ The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.☐The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Highlights  Equitable sharing of eligible research participants across multiple COVID-19 studies  Automated study eligibility determination using real-time EHR and REDCap integration  Researcher awareness and recruitment support using a central eligibility dashboard  Enhancing patient privacy and limiting participant fatigue in COVID-19 research