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Data and Data Collection

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  • Topic: Data and data collection
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Community-Level Interventions to Collect Race/Ethnicity and Language Data to Reduce Disparities

September 1, 2012 | Journal Article

This paper examines the experience of 14 Aligning Forces for Quality (AF4Q) alliances (data from additional alliances that joined the AF4Q initiative in 2009-2010 are not included in this analysis). This study’s target population included AF4Q allia ...

We're Glad You Could Join Us at Health Data Initiative III: The Health Datapalooza!

June 5, 2012 | Story

RWJF became one of the founding organizations of the Health Data Consortium, which was formed to encourage the creation of a health data ecosystem that promotes and accelerates the innovative use of health data.

Helping States Improve Data Reporting Efforts

May 24, 2011 | Program Result

The National Association of Health Data Organizations (NAHDO) worked to improve state reporting on the quality of hospital-based and other health care and coordinated state and national efforts to standardize reports on the quality of health care.

Getting Started With Your Own Pilot: Conducting Initial Data Analysis

February 27, 2011 | Toolkit

You can conduct your own analysis through the ECR Analysis Tool on the HCI3 website.

Getting the Data Right to Address Disparities in Health Care in New Jersey

August 27, 2009 | Program Result

The Health Research and Educational Trust worked with New Jersey hospitals to improve the procedures hospital staff uses to collect data about patients' race and ethnicity.

Hospitals Collect Race, Language and Ethnicity Data But Do Not Use it to Improve Quality of Care

July 29, 2009 | Program Result

Telephone surveys show how acute-care hospitals collect data on race, ethnicity and language and whether and how they use that data to improve quality of patient care.

Respondents Favor Legislation Allowing Collection of Racial, Ethnic Data to Improve Health Care

November 1, 2005 | Program Result

Researchers at Public Opinion Strategies conducted a national telephone survey of people's attitudes toward collecting racial and ethnic data for health care purposes.

How to Engage the Public's Interest in Health Care Quality Data: Financial Incentives

October 31, 2008 | Program Result

Health care quality has received considerable expert attention in the past decade, but there is little evidence that consumers are seeking out information about the quality of care that providers offer.

Chapter 5: Direct REL Data Collection Methods

September 5, 2008 | Toolkit

In 2003 to 2004, America's Health Insurance Plans collaborated with RWJF to conduct a survey and follow-up research to assess whether health plans and insurers collect racial and ethnic data and how this data is used to improve patient care.

Section 5: Case Studies

September 5, 2008 | Toolkit

The National Health Plan Collaborative Toolkit

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