Bonus: The improvement activity carries a higher-than-average weight. If you’re still collecting data to submit to the Quality Payment Program (QPP) in 2020 — and are involved in clinical trials related to COVID-19 — the feds have a potentially attractive new option available. Background: On April 20, the Centers for Medicare & Medicaid Services (CMS) added a new submission option for Merit-Based Incentive Payment System (MIPS) participants. The update encourages MIPS-eligible clinicians working on COVID-19 research to use that data to attest under the Improvement Activities category and offers higher-than-usual weight to the submission. The clinical trial attestations would garner providers like physicians, physician assistants, nurse practitioners, and others 20 points out of the 40 possible under the Improvement Activities category, relates an April 28 “Dear Clinician” letter from the agency. See How This Option Impacts Overall Scoring Remember, MIPS is made up of four separate performance categories — Cost, Improvement Activities, Quality, and Promoting Interoperability — that are each assigned a specific weight. Then those category points are combined for a total MIPS final score, which determines the positive or negative adjustment to your Medicare incentive reimbursement. Refresher: Here’s a breakdown of the MIPS 2020 performance period/2022 payment year numbers, including category weights and threshold totals: “By law, the Cost and Quality performance categories must be equally weighted at 30 percent beginning in the 2022 performance period,” according to the PY 2020 final rule fact sheet (see Medicare Compliance & Reimbursement, Vol. 45, No.23). Now: With the addition of the new COVID-19 Clinical Trials (IA_ERP_3) improvement activity option, interested MIPS providers will be able to capture half their IA points in one activity to reach the 15-percent category total. This offering aligns with agency efforts to provide relief for burdened clinicians struggling with the constraints of the pandemic and trying to compile measures for 2020 reporting. According to the details, “clinicians must attest to participation in a COVID-19 clinical trial utilizing a drug or biological product to treat a patient with a COVID-19 infection and report their findings through a clinical data repository or clinical data registry for the duration of their study,” advises the “Dear Clinician” letter. An example of an acceptable clinical trial might be a provider’s participation in National Institute of Health (NIH) research or through a clinical data repository, “such as Oracle’s COVID-19 Therapeutic Learning System,” CMS suggests. IT input: The agency also encourages MIPS-eligible clinicians to utilize open source data tools for uploading clinical trials’ submissions materials as the technology has a two-fold benefit. Not only does it show up more quickly in the system, but the research will improve “care delivery and the ability to treat COVID-19 patients” in the field, stresses the release. “CMS is supporting efforts of researchers to obtain solid, actionable data to accelerate the development of new treatments and our understanding of the coronavirus,” said CMS Administrator Seema Verma in a release. “Today’s action encourages clinicians to report data that will help us monitor the spread of the virus, find innovative medical solutions, and unleash scientific discovery as we seek to overcome this terrible disease.” Resources: Read the “Dear Clinician” letter at www.cms.gov/files/document/covid-cms-letter-qpp-mips-clinicians.pdf and reach the clinical trials database at https://clinicaltrials.gov.