Characterizing Caregiving Networks among Persons with ADRD in a Global Context
More than 80% of persons living with Alzheimer's Disease and Related Dementias (ADRD) receive care from one or more of their family members or friends.1 This proportion is even higher among individuals from low- and middle-income countries (LMICs) such as China where high-quality institutional and community care for dementia is limited.2 Prior studies have shown that dementia interventions can improve the health and well-being of persons with ADRD.3 However, most of these programs are intense, multicomponent, resource-demanding, focus only on the primary caregiver, and have mainly been