[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[H.R. 7717 Introduced in House (IH)]
<DOC>
119th CONGRESS
2d Session
H. R. 7717
To establish a pilot program at the Centers for Disease Control and
Prevention to support local jurisdictions in developing neighborhood-
level, publicly accessible health data platforms, to establish a
National Neighborhood Health Data Repository, and for other purposes.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
February 25, 2026
Mr. Torres of New York introduced the following bill; which was
referred to the Committee on Energy and Commerce
_______________________________________________________________________
A BILL
To establish a pilot program at the Centers for Disease Control and
Prevention to support local jurisdictions in developing neighborhood-
level, publicly accessible health data platforms, to establish a
National Neighborhood Health Data Repository, and for other purposes.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``Community Health Profiles Act''.
SEC. 2. COMMUNITY HEALTH DATA PILOT PROGRAM.
(a) Establishment.--Not later than 1 year after the date of
enactment of this Act, the Secretary of Health and Human Services,
acting through the Director of the Centers for Disease Control and
Prevention (in this section referred to as the ``Secretary''), shall
establish a pilot program (in this section referred to as the
``Program'') to award grants, on a competitive basis, to not more than
25 eligible entities to develop or enhance neighborhood-level, publicly
accessible health data platforms. Such platforms shall submit de-
identified, aggregated data to the National Neighborhood Health Data
Repository established under subsection (h), consistent with applicable
Federal, State, and local privacy laws.
(b) Program Objectives.--The objectives of the Program shall be
to--
(1) promote equitable access to local health data;
(2) support the integration of Federal, State, and local
surveillance systems into user-friendly, publicly accessible
health data platforms;
(3) facilitate data-driven public health planning and
community engagement;
(4) provide actionable insights at the State and local
level, with a focus on addressing health disparities; and
(5) support the establishment and maintenance of the
National Neighborhood Health Data Repository to enable national
comparability while upholding local data privacy standards.
(c) Eligible Entities.--To be eligible for a grant under the
Program, an entity shall be--
(1) a State or local health department; or
(2) a municipality or county government.
(d) Partnership With Academic and Nonprofit Institutions.--In
administering a grant under the Program, an eligible entity may partner
with an academic or nonprofit institution.
(e) Priority.--In awarding grants under the Program, the
Secretary--
(1) shall prioritize eligible entities that--
(A) serve populations experiencing health
disparities, such as medically underserved communities,
low-income communities, or environmentally burdened
communities;
(B) lack a neighborhood-level, publicly accessible
health data system; and
(C) demonstrate plans to use the data collected
from such a system to reduce health disparities; and
(2) may prioritize eligible entities that propose
innovative indicators beyond traditional public health
surveillance (pursuant to subsection (f)(1)).
(f) Use of Funds.--A grant under the Program may only be used to--
(1) develop or expand a publicly accessible health data
platform to provide neighborhood-level data across key domains,
including--
(A) social and economic conditions, such as
education, economic stress, neighborhood, violence, and
incarceration;
(B) housing and neighborhood conditions, such as
the prevalence and quality of air conditioners, housing
quality, and the quality of the built environment;
(C) maternal and child health;
(D) healthy living, such as self-reported health
status;
(E) health care, such as access to care and
avoidable hospitalization and vaccination; and
(F) health outcomes, such as chronic conditions,
the prevalence or treatment of human immunodeficiency
virus (commonly known as ``HIV'') and Hepatitis C,
binge drinking and psychiatric hospitalizations, infant
mortality and premature death, and life expectancy;
(2) integrate data from multiple sources, including--
(A) Federal surveillance systems;
(B) State and local administrative survey data; and
(C) local education, housing, and public safety
data;
(3) ensure data disaggregation by neighborhood, ZIP code,
or census tract, and support comparability across local
jurisdictions where feasible;
(4) design neighborhood-level, publicly accessible health
data platforms with clear citation of sources and transparent
methodology;
(5) incorporate into such platforms--
(A) visualization tools, such as charts, maps, and
trend lines; and
(B) downloadable datasets for public use;
(6) provide training or technical assistance to community
and local institutions to ensure sustainability and usability
of such platforms, including assistance in aligning such
platforms with Federal interoperability standards and model
legal frameworks for privacy, confidentiality, and data-sharing
compliance; and
(7) submit de-identified, aggregated data collected or
generated using grant funds under the Program to the National
Neighborhood Health Data Repository, in such standardized
format as the Secretary may require.
(g) Administration and Evaluation.--
(1) Administration.--In administering the Program, the
Secretary shall--
(A) issue program guidance and technical assistance
for platform development, data integration, and public
accessibility, including--
(i) standards for secure data reporting to
the National Neighborhood Health Data
Repository and alignment with Federal, State,
and local laws; and
(ii) model provisions on confidentiality
and comparability;
(B) provide technical assistance to grant
recipients on data methodology, privacy protection, and
system interoperability; and
(C) facilitate collaboration and peer learning
among grant recipients to share best practices and
promote replicability.
(2) Evaluation.--
(A) Initial report.--Not later than 1 year after
the establishment of the Program, the Secretary shall
submit to Congress a report that--
(i) summarizes the outcomes of the Program
and the progress made on the development of
neighborhood-level, publicly accessible health
data platforms;
(ii) assesses improvements the Program has
made in public access to health data, data
usability, and community engagement; and
(iii) identifies lessons learned and makes
recommendations for whether and how the Program
could be expanded nationally or extended beyond
the 4-year termination period described in
subsection (k).
(B) Updates.--The Secretary may update or
supplement the report described in subparagraph (A) as
the Secretary determines appropriate.
(h) National Neighborhood Health Data Repository.--
(1) Establishment.--The Secretary shall establish and
maintain a publicly accessible, searchable National
Neighborhood Health Data Repository to aggregate de-identified,
neighborhood-level health data from recipients of grants under
the Program.
(2) Elements.--The Repository shall--
(A) display data submitted by recipients of grants
under the Program;
(B) enable comparisons across local jurisdictions;
and
(C) include tools for visualization, filtering, and
downloading of data.
(3) Oversight.--The Secretary shall provide oversight of
the Repository by--
(A) reviewing data submissions;
(B) developing and implementing a methodology for
the aggregation of health data as described in
paragraph (4); and
(C) in consultation with States and local
jurisdictions, enforcing national data standards for
quality and consistency.
(4) Review of methodology by independent panel.--
(A) Establishment.--The Secretary shall establish
an independent advisory panel (in this paragraph
referred to as the ``panel'') for the purposes of
reviewing the methodology developed by the Secretary
under subparagraph (C).
(B) Appointment of members.--The Comptroller
General of the United States shall develop, maintain,
and make publicly available a list of nominees to serve
as members of the panel. The Secretary shall appoint a
member of the panel only after reviewing such list.
Such members shall be experts in epidemiology,
statistics, public health surveillance, and data
privacy.
(C) Review authority.--The Secretary shall develop
and implement a methodology for the aggregation of
health data for the purposes of the Repository, which
shall go into effect only upon certification by the
panel that such methodology--
(i) reflects scientific best practices; and
(ii) maintains public accessibility,
privacy protections, and data comparability
across jurisdictions.
(i) Definitions.--In this section:
(1) Health disparity.--The term ``health disparity'' means
a difference in health outcomes or access to health services
that is closely linked to social, economic, environmental,
racial, ethnic, or other demographic factors.
(2) Local jurisdiction.--The term ``local jurisdiction''
means a municipality, county, local health department, or
regional public health authority with the capacity to implement
a neighborhood-level, publicly accessible health data platform.
(3) Medically underserved community.--The term ``medically
underserved community'' has the meaning given such term in
section 799B of the Public Health Service Act (42 U.S.C. 295p).
(4) National neighborhood health data repository.--The term
``National Neighborhood Health Data Repository'' means the
National Neighborhood Health Data Repository established under
subsection (h).
(5) Neighborhood-level.--The term ``neighborhood-level''
means, with respect to a publicly accessible health data
platform, that such health data platform focuses on a
geographic area within a local jurisdiction that is smaller
than the municipal or county level, such as a ZIP code, census
tract, or community district.
(6) Publicly accessible health data platform.--The term
``publicly accessible health data platform'' means an online
tool, website, or dashboard that makes health data accessible
to the general public through visualizations, downloadable
datasets, or written summaries.
(j) Rule of Construction.--Nothing in this section shall be
construed to preempt or supersede any applicable Federal, State, or
local privacy laws.
(k) Termination.--The Program shall terminate on the date that is 4
years after the date on which the Secretary establishes the Program.
<all>
Community Health Profiles Act
#7717 | HR Congress #119
Policy Area: Health
Subjects:
Last Action: Referred to the House Committee on Energy and Commerce. (2/25/2026)
Bill Text Source: Congress.gov
Summary and Impacts
Original Text