Improving Data Infrastructure for Person-Centered Outcomes Research on Intellectual and Developmental Disabilities

Author:

Dhopeshwarkar Rina1,Jiménez Frances1,Ryan Sofia1,Plourde Emma2,Karimi Madjid3

Affiliation:

1. Rina Dhopeshwarkar, Frances Jiménez, and Sofia Ryan, Health Sciences Department, NORC at the University of Chicago

2. Emma Plourde, Office of Behavioral Health, Disability, and Aging Policy, Assistant Secretary for Planning and Evaluation, U.S. Department of Health and Human Services.

3. Madjid Karimi, U.S. Department of Health and Human Services, Office of the Assistant Secretary for Planning and Evaluation (ASPE)

Abstract

Abstract Individuals with intellectual and developmental disabilities (IDD) continue to experience disparities in health and well-being despite improved provisions of person-centered care. Patient-centered outcomes research (PCOR) translates evidence into practice for meaningful outcomes. This piece describes findings from an environmental scan and stakeholder outreach to identify and prioritize opportunities to enhance IDD PCOR data infrastructure. These opportunities include developing a standardized research definition; advancing data standards for service systems; improving capture of IDD at point of care; developing standardized outcome measures; and encouraging Medicaid data use for IDD research. Within this piece, we discuss the implications of addressing data gaps for enhanced research. While the identified activities provide a path towards advancing IDD PCOR data infrastructure, collaborative efforts between government, researchers, and others are paramount.

Publisher

American Association on Intellectual and Developmental Disabilities (AAIDD)

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4. Case service report (RSA-911);Center for Large Data Research and Data Sharing in Rehabilitation. (n.d.),2023

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