Key collaborative partners |
Research enterprise (public and private, researchers and funders) |
Health care providers, including those providing home care |
Community-based support |
Patients and their family and friend caregivers |
Policy makers and payers |
An array of other essential partners (eg, government public health, foundations) |
Domains of engagement for key partners |
Formulating research questions and methods that address context |
Reporting and interpreting research findings with greater attention to context |
Disseminating findings and strengthening the evidence base in prevention, management, and care for persons with MCC |
Translating findings into plain language in the patient’s context |
Sustaining funding, advocacy, and other support for context in research and practice |
Ongoing measurement and monitoring of progress and impact |
Steps for building and sustaining collaborative partnership |
Enumerate specific strategic partners |
Establish common and compelling lexicons and stories |
Engage partners |
Foster innovation on context-informed research (eg, encourage funding announcements, FDA, IRBs to emphasize context-informed research) |
Foster incorporation of context in practice (eg, cross-cutting clinical guidelines, performance measures, and patient-caregiver self-care management practice) |
Continue reinforcing actions by partners |
Measure and monitor effects and modulate actions |
FDA = Federal Drug Administration; IRB = institutional review board; MCC = multiple chronic conditions.