Kaiser Permanente’s Department of Research and Evaluation in Southern California is 1 of 42 health systems selected to participate in a PCORI initiative.
New virtual, innovative clinical trial for adults at high risk for respiratory illnesses
Kaiser Permanente researchers to study Vascepa in people 50 and older with heart disease
By Sue Rochman
Senior Writer
Researchers at the Kaiser Permanente Northern California Division of Research have begun recruiting patients for a randomized pragmatic clinical trial that will be conducted entirely electronically and virtually. The trial, called MITIGATE, will investigate whether a drug currently used to reduce the risk of heart disease and stroke can also prevent or reduce the risk of complications from viral respiratory illnesses in older adults with heart disease.
“This trial is only possible because Kaiser Permanente is an integrated health care delivery system with comprehensive electronic health records,” says study co-leader Alan S. Go, MD, a physician research scientist at the Division of Research and regional medical director of the Kaiser Permanente Northern California Clinical Trials Program based at the Division of Research. “This would be very challenging to do in a more fragmented health care system where you don’t have the exclusive relationship with members that we do.”
To take part, a person must be a member of Kaiser Permanente Northern California, be age 50 years or older, have a diagnosis of atherosclerotic cardiovascular disease, and have a registered email address in order to provide informed consent electronically. A participant cannot have had COVID-19, be institutionalized, or have a life-limiting illness. Atherosclerotic cardiovascular disease is caused by the buildup of fat, cholesterol, and other substances, often referred to as plaque, in the walls of the blood vessels.
A pragmatic randomized trial evaluates a drug’s effectiveness in a real-world setting. This makes the results more broadly generalizable. “Most randomized trials have many inclusion and exclusion criteria,” says study co-leader Andrew P. Ambrosy, MD, a physician research scientist at the Division of Research and a cardiologist at The Permanente Medical Group. “We wanted to make this study real-world and generalizable. For that reason, we have streamlined the eligibility criteria and we are focusing on the high-risk patients for whom this drug already has an indication approved by the U.S. Food and Drug Administration.”
The trial’s design will also make it easier “to quickly put the drug into clinical care if it does prove to be beneficial,” adds Dr. Go.
Kaiser Permanente members who meet the study criteria will be pre-randomized into 2 groups. One group will be contacted to see if they are interested in taking part in the study; the other group will be passively monitored only through their medical records. Patients who enroll will take part in a telehealth informed consent process and have the study drug mailed to their home. A member of the research team will check in with trial participants monthly to see if they are taking their medication and address any problems or concerns.
This trial is only possible because Kaiser Permanente is an integrated health care delivery system with comprehensive electronic health records.
– Alan S. Go, MD, physician research scientist
Ultimately, the researchers will follow 1,500 patients taking the medication and 15,000 similar patients in the control group. The study drug, Vascepa® (icosapent ethyl), contains pure and stable high-dose eicosapentaenoic acid, an omega-3 fatty acid. Six months after the last patient is enrolled, the researchers will review all of the patients’ electronic health records to see whether those taking Vascepa were less likely to be diagnosed with an upper respiratory illness, or had a less severe illness if they did get sick.
“For a trial of this size and scope, the use of electronic health records to conduct a trial from recruitment and enrollment to outcome ascertainment is truly unprecedented,” says Dr. Ambrosy.
Vascepa is approved by the FDA to reduce the risk of heart attacks or strokes in people with heart disease or diabetes. Laboratory studies suggest the drug may also potentially have antiviral activity and anti-inflammatory effects, which could help reduce the risk of getting or becoming severely ill with a respiratory illness.
“People who have atherosclerotic cardiovascular disease are at higher risk for complications if they develop a respiratory illness ,” said Jacek Skarbinski, an infectious disease specialist in The Permanente Medical Group and adjunct investigator at the Division of Research. “We look forward to seeing if Vascepa reduces these complications.”
Sue Rochman is senior writer, Medical & Science Research, at the Kaiser Permanente Division of Research in Northern California. This is reprinted from the Division of Research website.