- Gathered baseline data on the information and transparency needs of Medicaid managed care enrollees; the challenges enrollees face when trying to secure the tools and information needed; and if or how MCOs are taking steps to meet those needs.
- Conducted a focus group with MCOs to gather their understanding of the information needs of Medicaid managed care enrollees and how they currently provide information to them.
- Conducted seven focus groups with Medicaid managed care enrollees from diverse ethnic/racial backgrounds in geographically diverse areas (Albany, Buffalo, Syracuse, and Queens) on the following questions:
- Have you ever been unable to get the care you think you need?
- What do you do if you don’t like your doctor? Do you know you are allowed to switch primary care providers/MCOs at any time? Do you know how to?
- What do you understand are your rights as a Medicaid managed care enrollee? Do you know you are allowed to file a complaint? Know how to?
- What do you do if you think your plan or doctor is not allowing you to get the care you need?
- Do you receive information about health service quality from MCOs? What is your perception of quality, and do you use quality to compare across providers?
- Summarized the following key findings from the enrollee focus groups in a final report:
- Medicaid enrollees reported receiving information from MCOs about their rights, what to do if they are dissatisfied with their services, how to file a complaint, and how to switch a health provider. However, this information was typically hard copy materials that were mailed to enrollees and complicated to understand, which presented challenges for enrollees with limited reading ability. Enrollees preferred receiving information from customer service representatives during phone calls.
- Enrollees identified provider communication as an important dimension of quality, along with timely and equitable treatment, regardless of insurance status.
Results from the focus groups provided information on people’s understanding of their rights as Medicaid enrollees and how to file a complaint, their experience accessing doctors and challenges faced when navigating the care delivery system (e.g., long wait times, substandard care, unequal treatment), knowledge of recourse to take if they are not receiving the care they think they need, and perceptions of quality and familiarity with sources to get information on the quality of their providers.
Although the project did provide some baseline information on the experiences and difficulties enrollees faced navigating the health care system and receiving equitable care, there were still information gaps regarding the information needs of Medicaid managed care enrollees. Additionally, the focus group with MCOs was conducted before the enrollee focus groups, thus missing an opportunity to share and discuss learnings from the enrollees with MCOs. Finally, limited information was collected from MCOs on their understanding of the information needs of their enrollees and the steps they were taking meet those needs. Consequently, the final report did not contain information on learnings from MCOs or provide recommendations for how MCOs could better address the information needs of enrollees.
As a result, a key objective of the project, which was to develop recommendations for how MCOs could improve addressing the information needs of enrollees, was not met. Although MMNY engaged the support of MCOs early on, there was not consistent participation throughout the project. Having some type of formal partnership with an MCO from the onset of the project might have mitigated this issue. As the only statewide coalition dedicated to advancing the interests of Medicaid beneficiaries, MMNY is focused on ensuring the viability of Medicaid and addressing pressing access issues being faced by beneficiaries. As such, the goal of this project to address information needs of MCO enrollees may not have aligned with the top priority interests of the grantee.
Co-Funding and Additional Funds Leveraged: N/A