As the nation grapples with soaring demand for mental health services amid a provider shortage, more psychologists are considering the benefits of digital therapeutics—evidence-based interventions available to patients on their mobile devices. These tools have the potential to help people struggling with substance use disorders, anxiety, insomnia, and other conditions.
But there is a major hurdle blocking widespread access: Using digital therapeutics in practice is not usually covered by health insurance. The costs for the software alone can range from approximately $300 to $1,500 annually—fees that are out of reach for many patients.
“If patients are forced to pay out of pocket for the products, this is not a sustainable business model,” said Vaile Wright, PhD, senior director for health care innovation in the Practice Directorate at APA.
It’s also not sustainable for the companies that create the products, Wright notes. For example, in April 2023, Pear Therapeutics—a company that developed apps to treat substance use disorders and insomnia—filed for bankruptcy. The company’s reSET product, used in conjunction with standard outpatient treatment for substance use disorders related to stimulants, cannabis, cocaine, and alcohol, was cleared by the Food and Drug Administration (FDA) in 2016—the first mental health digital therapeutic cleared by the agency. “Unless we find a traditional health care pathway to cover the cost, digital therapeutics companies will not likely make it in our country,” Wright said. “This would be a significant loss for patients because the technology has the potential to bring evidence-based treatment to people who may not have access to care through the traditional psychotherapy model.”
Momentum is building in a few states to address this reimbursement issue. Early this year, state legislators began considering bills that would authorize Medicaid reimbursement for digital therapeutics in Arkansas, Minnesota, Hawaii, Arizona, and Maryland.
And at the national level, U.S. Senators Jeanne Shaheen (D-New Hampshire) and Shelley Moore Capito (R-West Virginia) and U.S. Representatives Kevin Hern (R-Oklahoma) and Mike Thompson (D-California) reintroduced bills that would create a new benefit category in Medicare to pay for the software component of these tools. To make these mental health interventions more accessible to the public during the pandemic, the FDA also streamlined the formal clearance process.
Although the federal and state bills are encouraging signs for advocates of these products, many of the bills limit which providers can use them and which fees are deemed reimbursable. “Payers should not only cover the cost of the software but also the provider time used to identify the appropriate digital therapeutic, teach the patient to use it, and monitor the patient’s progress,” said Wright.


