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This document provides guidelines and instructions for conducting a Health Equity Impact Assessment (HEIA) required by New York State legislation for health care facilities submitting Certificate of Need applications. It outlines the structure, definitions, and detailed steps for assessing potential health equity impacts of proposed projects on medically underserved groups.
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How to fill out health equity impact assessment

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How to fill out health equity impact assessment

01
Identify the health issue or project that needs assessment.
02
Gather relevant data on the population affected, including demographics and health outcomes.
03
Engage stakeholders, including community members and organizations, to gather insights and perspectives.
04
Assess existing health inequalities in the community.
05
Analyze how the proposed project or policy may impact different population groups.
06
Create recommendations to mitigate negative impacts and enhance positive effects on health equity.
07
Prepare a report summarizing findings and recommendations.
08
Share the assessment with stakeholders and implement feedback.

Who needs health equity impact assessment?

01
Public health officials and policymakers.
02
Community organizations and advocacy groups.
03
Healthcare providers and institutions.
04
Researchers studying health disparities.
05
Any organization implementing health-related programs or policies.
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Health equity impact assessment is a systematic process used to evaluate the potential effects of proposed policies, programs, or initiatives on health disparities among different population groups.
Entities such as government agencies, organizations implementing health-related programs, and policymakers are typically required to file health equity impact assessments.
To fill out a health equity impact assessment, one should identify the policy or program, assess its potential impacts on health equity, engage with affected communities, and compile findings in a structured format.
The purpose of health equity impact assessment is to identify and mitigate potential adverse effects of decisions on health equity, ensuring that all population groups benefit equally from health policies.
The information that must be reported typically includes the description of the policy, stakeholder engagement results, identified health disparities, assessment of impacts, and recommendations for improving equity.
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