Pillar II:
Data, Research and Evaluation


Native Hawaiians and Pacific Islander (NHPI) health data is often aggregated with Asian Americans despite the 1997 Revisions to the Standards for the Classification of Federal Data on Race and Ethnicity. The aim of Pillar II (Data, Research and Evaluation) is to implement strategies to increase PI-specific data, program evaluation and research.

Support Data Collection

Support the collection, management, and reporting of Pacific Islander health data and sharing of clinical information among Primary Care Providers.

Enhance Data

Enhance the collection, sharing and disaggregating of Pacific Islander heath data.

Improve Data Sharing

Improve continuity of care for COFA migrant patients through sharing and exchange of clinical information.

Engage Researchers

Engage Pacific Islander (PI) researchers and communities to conduct primary health care research.

How can we work together?

How can we work together?