A community-engaged health care model that shifts power and agency to underserved patients may lead to more responsive and accessible care.

A set of resources and strategies to help health care stakeholders foster authentic, effective community engagement that drives local policy and program change.

Website offers a qualitative database of personal narratives to support providers and policymakers in designing policies that better reflect the lived experience, needs, and priorities of older adults.

Toolkit offers recommendations and examples for screening and interventions that support social connectivity of older adults.

Facilitated telemedicine for hepatitis C among opioid use disorder patients in opioid treatment programs resulted in substantially higher cure rates than standard-of-care off-site referrals.

This resource center offers guidance to help Medicaid stakeholders engage community members in policy and program design development, especially as a means of increasing health equity.

Report summarizes the evidence on outcomes for patients participating in various telehealth delivered services, including different modalities, such as telephone and video.

Rethinking eligibility, beyond cost and utilization, offers a more equitable approach to identify high-need individuals for care management.

Describes how community-based participatory action research, especially in peer-based mental health settings, can advance community empowerment and health equity.

Black caregivers of people with dementia share their perspectives on a care coordination intervention.

Offers practical recommendations to improve telemedicine interventions to be more equitable for diverse populations, particularly those with low incomes.

Includes patient- and staff-reported measures to help complex care programs better understand the impacts of interventions.

Health care organizations can use population-level data sources about the experiences of people with disabilities to improve care.