Is your data equitable?

The UCLA Data Equity Center offers resources and technical assistance to help you achieve your goals to ensure that your data is representative and inclusive and reflects collaborative efforts with the communities you serve to address their needs.
 

Topics
Resource Type
Blog Post

Duke University, Dept of Sociology

News Tip: ‘Reliability’ Concerns With New Federal Standards For Collecting Data on Race, Expert Says

Jen’nan Read

Race and Ethnicity

This brief post makes the case for the Census on the new Middle East and North Africa (MENA) box data compared to previous modes for collection of ancestry data. 

Journal Article

American Journal of Public Health

Lack of Arab or Middle Eastern and North African Health Data Undermines Assessment of Health Disparities

Germine H. Awad, Nadia N. Abuelezam, et al.

Race and Ethnicity

This brief article makes the case for collection of a Middle East and North Africa (MENA) category, and outlines collection methods or strategies.

Journal Article

Journal of Racial and Ethnic Health Disparities

Development of an Ethnic Identity Measure for Americans of Middle Eastern and North African Descent: Initial Psychometric Properties, Sociodemographic, and Health Correlates

Ken Resnicow, Minal R. Patel, et al.

Race and Ethnicity

Using data from 375 Arab and MENA people, the paper outlines a new MENA ethnic identity scale.

Blog Post

US Census Bureau

3.5 Million Reported Middle Eastern and North African Descent in 2020

Rachel Marks, Paul Jacobs, Alli Coritz

Race and Ethnicity

This post details the results of the 2020 Census and it’s collection of detailed MENA data, disaggregated from the white racial box. Until the new OMB racial and ethnic directives are implemented, this is the largest data set on how ethnic directives are implemented, this is the largest data set on how MENA community MENA community identifies.

Report

Urban Institute

Missing Data: A Framework for Addressing Equity in Measurement

Amanda Astrea, Melissa Botein, Sarah Beth Kaufman

Missing data

This report provides a clear and concise overview of missing data issues and their impact on equity measures. It outlines a framework for addressing these issues and ensuring fair and accurate data analysis.

Report

Data & Society Research Institute

How Missing Data Can Perpetuate Bias

Sarah Brayne

Missing data

This blog post explains the concept of missing data and how it can lead to biased results, particularly when analyzing issues of equity. It uses clear language and real-world examples to make the topic accessible to a broader audience.

Report

AHRQ, USDHHS

Medical Expenditure Survey Supplement: Understanding Veteran’s Health Care Needs

Agency for Healthcare Research and Quality's (AHRQ), United States Department of Health and Human Services (USDHHS)

Status and Identity

Survey was developed to understand the health care needs and utilization of military veterans.

Report

AHRQ, USDHHS

Understanding Veterans’ Healthcare Use and Experience, 2018–2019

Didem M. Bernard, Abigail Woodroffe, Siying Liu

Status and Identity

This report examines the prevalence of selected medical conditions, use of healthcare both inside and outside of the healthcare system of the Department of Veterans Affairs (VA), and experience with VA and non-VA healthcare providers among Veterans in the U.S. civilian non-institutionalized population.

Webpage

AAMC Center for Health Justice

Association of American Medical Colleges (AAMC) Principles of Trustworthiness

Since 2015, the AAMC has produced an annual series of Community Engagement Toolkits in collaboration with our members and their communities. These toolkits provide unvarnished community perspectives on crucial issues and views about how members can be better partners. 

Webpage

Office of Minority Health (OMH)

Explanation of Data Standards for Race, Ethnicity, Sex, Primary Language, and Disability

Race and Ethnicity

HHS examined current Federal data collection standards, adequacy of prior testing, and quality of the data produced in prior surveys, consulted with statistical agencies and programs, reviewed Office of Management and Budget (OMB) data collection standards and the Institute of Medicine (IOM) Report Race, Ethnicity, and Language Data Collection: Standardization for Health Care Quality Improvement and built on its members' experience with collecting and analyzing demographic data.