Barriers and Motivators Associated With Access to Care and Participation in Research Studies for Parkinson's Disease Among Asian Americans
Barriers and Motivators Associated With Access to Care and Participation in Research Studies for Parkinson's Disease Among Asian Americans
The ultimate goal of this project is to use the findings to develop culturally appropriate programs and resources that can be disseminated to key stakeholders to improve access to PD care and increase inclusivity in PD research for Asian Americans. This study will serve as a first step towards developing broader community and patient education programs and active outreach campaigns to increase PD-specific literacy among Asian Americans. The results from this study will elucidate the role that language barriers, cultural perceptions, family influence, and other predisposing, enabling, or need factors have on delaying care for PD among Asian Americans. It will also provide much needed insight on how to improve inclusion of Asian Americans in PD research studies.
Inclusion Criteria:
Objective 1 (chart review):
Objective 2 (qualitative study):
Asian American person diagnosed with PD:
Primary caregivers of Asian American PD patients recruited into the study:
Clinicians:
Key advocates in the Asian American community working specifically with the Asian elderly population.
Employee or volunteer for a community-based organization working with the Asian elderly population (e.g. Greater Boston Chinese Golden Age Center, South Cove Manor, and Midtown Home Health Services) or other organizations working with PD patients and the elderly (e.g. Massachusetts Council on Aging and the Massachusetts Chapter of the American Parkinson's Disease Association)
Age: 18 years of age or older
Able to participate in a focus group discussion on Zoom
Objective 3 (surveys of care partners of Asian American individuals with PD):
Exclusion Criteria:
Objective 1:
1. Patients diagnosed with juvenile-onset Parkinson's Disease
Objective 2:
PD patients only:
No exclusion criteria for other stakeholder groups (caregivers, clinical providers, key community advocates).
Objective 3:
1. Patients with juvenile-onset Parkinson's Disease
alice.tang@tufts.edu617-636-2140
nesar@asianwomenforhealth.org