Toolkit offers health care stakeholders interested in working with community members guidance on equitable compensation strategies.

This report outlines practical approaches to guide health systems in more meaningfully involving community members and being more accountable to the communities they serve.

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.

This webinar featured a rural Pennsylvania partnership and its experience implementing trauma-informed care across a network of providers.

A novel street psychiatry program offers essential mental health support to unsheltered individuals experiencing homelessness.

A collaborative interprofessional dementia care program significantly improved the timeliness of diagnosis compared to traditional clinics and achieved high satisfaction rates among staff, patients, and caregivers.

A provider tool that promotes person-centered and equitable care by recognizing and avoiding bias in electronic health record notes.

Highlighted how Denver Health, a large health system in Colorado, is integrating a trauma- and resilience-informed approach into organization-wide policy and practice.

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

Details the main elements of a hospital-based addiction care consultation team.

Recommendations for building a stronger, more coordinated, and patient-centered complex care evidence base.

Patients with higher ACEs scores or positive PTSD screenings felt stress when seeking medical care, but indicated trauma-informed treatment approaches would relieve this stress.

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

Some person-centered care interventions are more effective than others at reducing behavioral and psychological symptoms and improving cognitive function in people with dementia.

Home-based primary care did not decrease hospitalizations for people with dementia, but it did result in more patient- and family-centered end-of-life care.

Telephone- and web-based dementia care provided through centralized hubs and delivered by an interdisciplinary team can improve outcomes for people with dementia and their caregivers.

Training for caregivers of veterans living with dementia may help them remain in their home longer, but may lead to increased health care costs.

Dementia care program delivered by an occupational therapist and tailored to the needs of patients and their caregivers shows improved patient quality of life and caregiver well-being.

Details implementation guidance for the evidence-based Care Ecosystem model, which improves supports for people with dementia and their caregivers.

For people with disabilities, familiarity with their care teams and care plans, and increased access to long-term services and supports can improve their perceptions of quality of life and health care.