The objective of the Health Disparities & Intellectual Disabilities project is to inform efforts to (a) improve the capacity of current health surveillance systems to track the health and healthcare of people with intellectual disabilities and (b) increase the effectiveness of health-related practices, services, and programs that influence the lives of people with intellectual disabilities.
To achieve this overall aim, this project will pursue four specific aims:
- Data Sources. The project will identify the set of valid and reliable data sources that maximize the quality of information (e.g., population-based statistics and research findings), given the needs of the target audience (i.e., public health practitioners, administrators, and researchers) and the strengths and weaknesses of existing data. And conversely, the project will identify ways to improve existing data sources that are currently inadequate for studying the population with intellectual disabilities.
- Key Variables. The project will use this subset of existing data sources to identify an array of key variables to facilitate the study of the risk and protective factors associated with disparities between the populations with and without intellectual disabilities. This subset will include dependent variables—selected from the leading health Indicators and/or frequently cited unmet healthcare needs—and independent variables from frequently cited protective factors and risk factors, including personal and household characteristics, the utilization of services, and barriers and facilitators within physical, social, economic, and healthcare environments.
- Analyses. The project will use this array of key variables (and corresponding data sources) to develop and estimate empirical models that identify the factors associated with disparities between the populations with and without intellectual disabilities.
- Knowledge Translation. The project will disseminate the results of our activities to public health practitioners, administrators, and researchers (i.e., the projects target audience) in a manner that facilitates their efforts to reduce health disparities between people with and without intellectual disabilities and improve data collection. This includes sharing the data itself, conveying the results of our efforts to identify valid and reliable data (e.g., options for improving upon existing data sources), and summarizing the findings of our analyses. Dissemination materials will meet the learning styles of audience members.