Through Epic, we now have the ability to invite patients to studies using MyChart. Inviting patients to participate in research studies through MyChart is a new recruitment approach. In an effort to reduce unnecessary communication, the messages are targeted to patients who may be interested and eligible for studies. The use of MyChart for recruitment requires IRB approval, and extensive care is taken to protect patient privacy. To safeguard patient privacy, PIs and research teams will not be able to see PHI.
Patients can always opt out of receiving future invitations through MyChart. A patient may either email us at email@example.com or request their provider opt them out by adding an “FYI Flag” to cont contact for research to their Epic Account. We are in the early stages of MyChart recruitment and 4 patients, out of several thousand contacted, requested to opt out.
In a recent survey, we assessed what patients think about MyChart research invitations; 90 percent of surveyed patients agreed that invitations to join research studies are an appropriate use of MyChart. Sixty percent reported that it did not change their satisfaction with being a patient at Johns Hopkins and 40 percent reported that it increased their satisfaction with being a patient at Johns Hopkins. Patients can always opt out of receiving future research invitations through MyChart.
Here are images of what your patient may see when they open MyChart:
MyChart Recruitment Service is a collaboration between data analysts, experts in recruitment methods, and clinical researchers that offers a secure method of electronically recruiting potential research participants. Target populations are identified and reached through database queries that are embedded in Epic. Potential participants are messaged via their activated Johns Hopkins MyChart account. Team members at The Office of Recruitment within The Institute for Clinical and Translational Research (ICTR) work together to manage this service. Our goal is to support ongoing research at Johns Hopkins, while also empowering and engaging patients by connecting them with clinical research studies that may be of interest to them.
MyChart Recruitment Service is offered by the Research Participant and Community Partnership Core of the Institute for Clinical & Translational Research (Deputy Director, Cheryl Dennison Himmelfarb). Cassia Lewis-Land manages the day to day operations of the service with support by Kelly Gleason, RN, PhD, Hailey Miller, RN, and the CCDA (Center for Data Analytics) team.
The timeline varies depending on the pace of the study team. The ICTR MyChart team and CCDA will work thoroughly with the study team to ensure a smooth process. Once a study team chooses to utilize MyChart to send research invitations, approval is sought from the MyChart Epic Research Council. An approval letter from the council is submitted by the research team along with the protocol for IRB review and approval. After the IRB approves MyChart as a recruitment strategy, we collaborate with the CCDA to create a SQL query, which is used to generate an Epic report of the target population.
The majority of the work by the study team is completed in the preliminary steps of the process. After the team has IRB approval and the report is generated, the team will establish a timeline and calendar with the MyChart team members. From that point, the MyChart team will handle the sending of messages on a regular basis. As the process is ongoing, the MyChart team will ask study teams to track messages and inquiry rates from our service. The MyChart team will explain this process to the study team before messages are started.
After the initial report is generated and messages begin sending, study teams can only change their original inclusion/exclusion criteria if they retract the original report from production and pay for the services again. This process takes several weeks, although is possible.
A regular calendar will be established with the MyChart team as you begin. Depending on the size of the report, different frequencies can be established. Study teams choose different frequencies, ranging from every week to every month. This can be adjusted throughout the process.
The report size varies depending on a study team’s population of interest and exclusion/inclusion criteria. Bulk messages are sent out to 200-1,000 people at a time depending on population vulnerability and report size.
Teams interested in our service are encouraged to contact us at: Research_Recruitment@jhu.edu. Teams should be aware the service cost ranges from $1,000- 3,000 depending on the complexity of the query created and other factors of work effort. The CCDA provides free consults and can provide researchers with an idea of pricing so that they can allot a proper amount in budgeting for their project.
Early Peanut Introduction- Translation to Clinical Practice
Infants and pediatrics (0-8)
Robert Findling and Marco A. Grados
Adolescent Mood Disorders
EMPower: Electronic Media Powering positive health changes in youth
Anemia in females
Mark C. Liu
Cathelicidin and Vitamin D: Impact on Populations At-Risk and with COPD
Young to Older Adults (18-80)
Clinical Trial of Air Cleaners to Improve Indoor Air Quality and COPD Health
Middle-Aged &Older Adults (>40)
Brain and food
Perinatal Mood Disorders
Pete Miller III
The Diet Gout Trial
1. Atrial Fibrillation
2. Diagnostics in the ER
STURDY: Fall reduction and Vitamin D
Older Adults (>70)
BDPP Treatment for Mild Cognitive Impairment and prediabetes or Type 2 Diabetes Mellitus
Middle-Aged & Older Adults (50-80)
Immune Cell Biology and Function in allergic disease
Young to Middle-aged Adults (18-45)
Daily 24 study
Cardiometabolic health in adolescents of south Asian ancestry
Neurobehavioral Correlates of Frustration in ADHD
The Medication Adherence Research in COPD (MARC) study