Family:
|
Caregiver capacity Caregiver health
literacy |
Standardize measures of household material
hardshipa
Standardize measures of key social determinants of
health
Develop community programs to address patient/family
social and material hardship
Increase psychosocial resources (social workers,
financial navigators) for caregivers
Provide educational and culturally tailored
interventions to improve caregiver health literacy
Increase access to care after hours and on
weekends
|
Healthcare
system:
|
Delivery of quality care |
Improve DEI in childhood cancer clinical
trials:
Align family trust with provider
cultural competence to engage
patients/families
Address regulatory and language
barriers
Include bilingual and culturally
competent study team members to enhance engagement
with minoritized patients/families
Invest in language translation and use
simplified, accessible language in consents
Implement institutional approaches and
metrics to overcome mistrust rooted in the history
of unethical research including minoritized
patients
Capture reasons for refusal and
ineligibility in trials
Incorporate patients’/families’ social
circumstances when tailoring and delivering patient-centered
care
Collect institutional data beyond 5-year survival:
disease-specific survival; postrelapse survival; early and
late noncancer mortality
Invest in transition to postcancer care
|
Community and
society:
|
Structural racism |
Utilize available data on geographic concentration
of deprivation in medical and health services research
Call for RFAs to study and inform policies to
eliminate modifiable and unjust drivers of structural
racism
|
Public policy |
|