Announcement of Requirements and Registration for “My Air, My Health Challenge”, 33742-33745 [2012-13834]
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33742
Federal Register / Vol. 77, No. 110 / Thursday, June 7, 2012 / Notices
Dated: May 31, 2012.
Farzad Mostashari,
National Coordinator for Health Information
Technology.
[FR Doc. 2012–13830 Filed 6–6–12; 8:45 am]
BILLING CODE 4150–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Announcement of Requirements and
Registration for ‘‘My Air, My Health
Challenge’’
Office of the National
Coordinator for Health Information
Technology, HHS. National Institute of
Environmental Health Sciences,
National Institutes of Health, HHS.
Award Approving Official: Farzad
Mostashari, National Coordinator for
Health Information Technology.
ACTION: Notice.
AGENCY:
Environmental and public
health are closely related and
complementary fields—and their future
depends on a closer understanding of
those connections. New portable sensors
have the potential to transform the way
we measure and interpret the influence
of pollution on health. These
technologies can provide a picture that
is more detailed and more personal,
with dramatic implications for health
care, air quality oversight, and
individuals’ control over their own
environments and health.
The U.S. Environmental Protection
Agency (EPA) and U.S. Department of
Health and Human Service (HHS)
[National Institute of Environmental
Health Sciences (NIEHS) and Office of
the National Coordinator for Health
Information Technology (ONC)]
envision a future in which powerful,
affordable, and portable sensors provide
a rich awareness of environmental
quality, moment-to-moment
physiological changes, and long-term
health outcomes. Health care will be
connected to the whole environment,
improving diagnosis, treatment, and
prevention at all levels.
Many of the first steps toward this
future have already been taken.
Prototype projects have developed
portable air quality and physiologic
sensors, and experimental analysis tools
for handling data that is higher quantity,
but often lower quality, than more
traditional monitoring techniques. The
‘‘My Air, My Health Challenge’’ aims to
build on this foundation. We are seeking
solutions that integrate data from
portable physiological and air quality
monitors, producing a combined picture
that is meaningful and usable. The
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SUMMARY:
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statutory authority for this challenge
competition is Section 105 of the
America COMPETES Reauthorization
Act of 2010 (Pub. L. 111–358) and
section 103 of the Clean Air Act, 42
U.S.C. 7403. This challenge addresses
the mission of the NIEHS to conduct
and support programs with respect to
factors in the environment that affect
human health, directly or indirectly. 42
U.S.C. 285.
DATES: Phase 1: Effective on June 6,
2012. Submission period ends October
5, 2012, 11:59 p.m. et. Phase 2: Effective
on November 19, 2012. Submission
period ends May 19, 2013, 11:59 p.m. et.
FOR FURTHER INFORMATION CONTACT:
Denice Shaw, EPA, 202–564–1108;
Adam Wong, ONC, 202–720–2866.
SUPPLEMENTARY INFORMATION:
Subject of Challenge Competition
The ‘‘My Air, My Health Challenge’’
is a multidisciplinary call to innovators
and software developers (‘‘Solvers’’) to
enable near-real-time, location-specific
monitoring and reporting of air
pollutants and potentially related
physiological parameters, using a
personal/portable integrated system to
assess connections between the two
(‘‘sensor systems’’). The system must
link air-pollutant concentrations with
physiological data, provide geocoded
and time-stamped files in an easy-to-use
format, and transmit this data via
existing networks to a central data
repository provided by EPA and HHS.
The challenge is structured in 2
phases:
Phase 1—Project Plan (no more than
15 pages, not including appendices that
may consist of diagrams/schematics,
bibliography, and other supplementary
materials).
1. Propose a plausible link between
health outcomes and airborne pollutants
(chemical species and/or particulates),
and provide evidence to support a
plausible and physiologically
meaningful relationship between
airborne pollutants and physiological
metrics in a defined population.
2. Propose a prototype design and
development plan for an integrated
multi-sensor and data management
system that may be easily worn or
carried by individuals within the
defined target community/population.
3. Conceptualize data generation,
management (may include processing &
on-board storage), and transmission
functionality of the device.
4. Propose a small-scale proof-ofconcept study to validate the proposed
prototype.
5. Study design process must include
input from the target community/
population.
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Phase 2—Proof-of-Concept Pilot
Project.
6. Finalists attend an event for
feedback, questions, and business/
entrepreneurial resources prepared by
Challenge sponsors (EPA, HHS ONC,
NIEHS).
7. Solvers develop the proposed
prototype and execute experimental
validation of the system to bring
together data from personal air quality
and physiological monitors, showing
how these types of data and sensors can
be integrated for practical use by health
and environmental agencies, and by
individual citizens. Proof-of-concept
data must illustrate the accuracy and
precision of the raw data and of any
processed data produced by the system.
Level of Focus for Health/Pollution
connections: Systems must track
airborne pollutants and physiological
parameters for a known or plausible
health-pollution link. Solvers must be
able to justify their chosen combination
with research citations and to optimize
the air sampling parameters (volume,
frequency, etc.) and physiological
measurement parameters to provide
resolution appropriate to the specific
pollutant, or combination of pollutants,
and related health implications.
Challenge Sponsors will provide
examples of such links for illustrative
purposes (appended to the challenge
announcement), but will not limit
Solvers to these particular cases.
Sensor development: Solvers are not
expected to develop novel sensors for
this challenge, but are not restricted to
commercially available sensors. They
may use sensors that are currently in the
development or piloting stage, but must
show that the sensor will be ready to
use in functional tests—at least at a
small scale—in time for the Phase 2
proof-of-concept demonstration.
Instruments must be well characterized
in terms of precision, accuracy and
sensitivity. Integrated sensor systems
must be able to transmit data to the
central repository (in real time, or store
and forward) using existing data
networks (e.g. 3G, LTE, or WiFi), or able
to connect with personal devices (e.g.,
smart phones) that have such capability.
Solvers must enable appropriate
calibration and error checking
capabilities, although these need not be
onboard the portable monitoring
components.
Data Requirements and Constraints:
Data transmitted by the integrated
devices to a centralized data repository
must enable the following to be
understood from transmitted data:
1. Indicators of device functionality,
including any results of automated
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system diagnostics, calibrations, or error
logs
2. The device unique identifier,
including any paired communication
device identifier (particularly important
if bidirectional communication
functionality is proposed)
3. Date and time the data were
collected/measurements made (start and
end timestamp)
4. The location of the device during
data collection (geocode)—if sampling
occurs over several minutes or longer
Solvers should consider that users may
be using transportation and that analysis
should ideally show locations between
sample start and end
5. Raw measurement data
(quantitative or semi-quantitative) as
well as any processed data or combined
6. Quality control metrics indicating,
for instance, whether the device is being
worn/carried or functioning correctly.
Error checking can occur either prior to
or after data transmission, but is an
essential component.
The preferred data transmission file
format is comma separated value (.csv)
or variants thereof. Alternatively,
encrypted binary files are also
acceptable. Encryption keys/codes
should be provided to the Challenge
Sponsors so that data can be accessed at
the central data repository.
Pollutant Focus: Solvers will be
required to include at least one air
pollution metric—although at their
discretion they may include multiple air
pollution metrics and/or other
environmental metrics such as noise
level and UV exposure. The focus,
however, will be on chemical and/or
particulate air pollutants.
Physiological Parameter Focus:
Solvers will be required to include at
least one physiological metric—
although at their discretion they may
include multiple physiological metrics
and/or other person-oriented metrics
such as behaviors and social
interactions. The focus, however, will
be on physical parameters (e.g., heart
rate, breathing, pulse oxygenation), and
their connection to pollutants.
Physical Guidelines for Sensors: At
least one component of the sensor
system must be wearable or carryable,
and all components should have a
minimal burden and be minimally
obtrusive. The overall sensor system
must focus on personal and local
metrics (i.e., measuring air quality in the
immediate vicinity of the wearer).
Wearable components must be the right
size and weight for their target audience
(e.g., no more than 300 g for a child).
Sampling frequency and area must be
appropriate to the pollutants and
physiological metrics of interest, as well
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as to the context of data collection (e.g.,
by walkers, cyclists or passengers on
public transportation). The sensor
system must include an on-board data
buffer for when network access is
unavailable, and may also at the
Solver’s discretion include personal
media to which data may be
downloaded for permanent or
temporary storage. Open source
hardware and software are desired but
not required.
Measurement Guidelines for Sensors:
Accuracy, detection limit, measurement
range, and sensitivity of all sensors must
be at sufficient resolution to record
health-relevant changes in air
pollutant(s) and physiological marker(s).
If processing of the data is required in
order to achieve this (e.g.,
normalization, increasing signal-tonoise ratios), the Solver must include
the algorithm and its scientific basis
(i.e., previously collected data and/or
appropriate citations) in their report.
Alternatively, centralized processing
that enables parsing of local data, in
order to increase data robustness and
reduce false positive signals, may be
used. If such an approach is determined
to be useful, Solvers must outline
suitable strategies and/or boundary
criteria. In either case, solvers must
communicate the overall uncertainty
level of the final system output
Community Involvement: The sensor
system must address a need in a specific
community or population. In addition to
scientific evidence supporting that
need, Solvers must also seek and
document community input.
Representatives of the affected
community should provide feedback on
the pilot project both during
conceptualization (Phase 1), and
throughout the pilot study (Phase 2).
This is not intended to override the
Solvers’ scientific judgment on
technical issues, but to ensure that the
project is respectful of local knowledge,
community identity, and needs. Projects
must include feedback to the
community regarding both technical
success (e.g., whether sensors performed
as planned) and results (e.g., any
correlations found in the data).
Scaling and Future Plans: While
Phase 2 requires only a small-scale
proof-of-concept project, final
submissions for this phase must include
a description of how the project could
or will be extended and expanded. In
general, Solvers are asked to propose
concrete next steps that might be carried
out with more time or resources
available.
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Eligibility Rules for Participating in the
Competition
To be eligible to win a prize under
this challenge, an individual or entity
shall have complied with all the
requirements under this section and
Federal Register Notice.
This challenge is open to any Solver
who is (1) an individual or team of U.S.
citizens or permanent residents of the
United States who are 18 years of age
and over, or (2) an entity incorporated
in and maintaining a primary place of
business in the United States. Foreign
citizens can participate as employees of
an entity that is properly incorporated
in the U.S. and maintains a primary
place of business in the U.S. Solvers
may submit more than one entry.
Eligibility for Phase 2 is conditional
upon being selected as a Phase 1
Finalist. Eligibility for a prize award is
contingent upon fulfilling all
requirements set forth herein. An
individual, team, or entity that is
currently on the Excluded Parties List
(https://www.epls.gov/) will not be
selected as a Finalist or Winner.
Employees of EPA, HHS, and the
reviewers or any other company or
individual involved with the design,
production, execution, or distribution of
the challenge and their immediate
family (spouse, parents and stepparents, siblings and step-siblings, and
children and step-children) and
household members (people who share
the same residence at least three (3)
months out of the year) are not eligible
to participate.
An individual or entity may not be a
Federal entity or Federal employee
acting within the scope of their
employment. Federal employees seeking
to participate in this challenge outside
the scope of their employment should
consult their ethics official prior to
developing a submission. An individual
or entity shall not be deemed ineligible
because the individual or entity used
Federal facilities or consulted with
Federal employees during a competition
if the facilities and employees are made
available to all individuals and entities
participating in the competition on an
equitable basis.
Federal grantees may not use Federal
funds to develop COMPETES Act
challenge applications unless consistent
with the purpose of their grant award.
(Grantees should consult with their
cognizant Grants Management Official
to make this determination.) Federal
contractors may not use Federal funds
from a contract to develop COMPETES
Act challenge applications or to fund
efforts in support of a COMPETES Act
challenge submission.
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Federal Register / Vol. 77, No. 110 / Thursday, June 7, 2012 / Notices
Liability and Indemnification: By
participating in this competition,
Solvers agree to assume any and all
risks and waive claims against the
Federal Government and its related
entities, except in the case of willful
misconduct, for any injury, death,
damage, or loss of property, revenue, or
profits, whether direct, indirect, or
consequential, arising from
participation in this competition,
whether the injury, death, damage, or
loss arises through negligence or
otherwise. By participating in this
competition, Solvers agree to indemnify
the Federal Government against third
party claims for damages arising from or
related to competition activities.
Insurance: Based on the subject
matter of the competition, the type of
work that it will possibly require, as
well as an analysis of the likelihood of
any claims for death, bodily injury, or
property damage, or loss potentially
resulting from competition
participation, Solvers are not required to
obtain liability insurance or
demonstrate financial responsibility in
order to participate in this competition.
Registration Process for Participants
To register for this challenge
participants may do any of the
following:
D Access the www.challenge.gov Web
site and search for the ‘‘My Air, My
Health Challenge’’.
D Access the ONC Investing in
Innovation (i2) Challenge Web site at:
Æ https://www.health2con.com/
devchallenge/challenges/onc-i2challenges/.
Æ A registration link for the challenge
can be found on the landing page under
the challenge description.
D Access the Innocentive challenge
Web site at www.innocentive.com/
myairmyhealth.
Amount of the Prize
D Phase 1: $15,000 each for up to four
Finalists who are selected to move on to
Phase 2.
D Phase 2: $100,000 to the Winner.
Awards may be subject to Federal
income taxes.
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Payment of the Prize
HHS and EPA prizes awarded under
this competition will be paid by
electronic funds transfer and may be
subject to Federal income taxes. HHS
and EPA will comply with the Internal
Revenue Service withholding and
reporting requirements, where
applicable.
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Basis Upon Which Winner Will Be
Selected
The review panel will make selections
based upon the following criteria in
Phase 1:
D Strength of evidence and/or
argumentation regarding the linkage
between air pollutant and physiological
effect.
D Potential significance of technology
and eventual benefit to target
population(s).
D Viability of proposed sensor
technologies to detect and quantify
pollutants and their effects, and provide
physiologically relevant health and air
quality data.
D Viability of the proposed data
reporting technology (communication to
a centralized data repository provided
by EPA and HHS)
D Viability of the proposed project
plan.
D Viability of the proposed
instrument design as a wearable/
portable device.
D Viability of the proposed proof-ofconcept study (low complexity is
preferred).
D Appropriate use of community
input in designing proof-of-concept
study.
The review panel will make selections
based upon the following criteria in
Phase 2:
D Sensors: Successful technical
collection of both health and
environmental data
D Data Reporting: Successful
formatting and transmission of data
D Data processing and evaluation
D Community Involvement and
Interaction
Additional Information
Intellectual Property Rights: Upon
submission, each Solver warrants that
he or she is the sole author and owner
of the work, that the work is wholly
original with the Solver (or is an
improved version of an existing work
that the Solver has sufficient rights to
use—including the substantial
improvement of existing open-source
work) and that it does not infringe any
copyright or any other rights of any
third party of which Solver is aware.
Each Solver also warrants that the work
is free of malware.
(a) Copyright. By participating in this
competition, each Solver hereby grants
to the Federal government an
irrevocable, paid-up, royalty-free,
nonexclusive worldwide license to
reproduce, distribute copies, display,
create derivative works, and publicly
post, link to, and share, the work or
parts thereof, including any parts for
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which it has obtained rights from a third
party, in any medium, for Federal
purposes. User warrants that it has
obtained rights to any parts of the work
not authored by Solver adequate to
convey the aforementioned license. (b)
Inventions. Finalists hereby grant to the
Federal government a nonexclusive,
nontransferable, irrevocable, paid-up
license to practice or have practiced for
or on behalf of the United States any
invention throughout the world made
by Finalists that, if patented, would
cover the submission or its use.
Privacy, Data Security, Ethics, and
Compliance
Solvers are required to identify and
address privacy and security issues in
their proposed projects, and describe
specific solutions for meeting them.
In addition to complying with
appropriate policies, procedures, and
protections for data that ensures all
privacy requirements and institutional
policies are met, use of data should not
allow the identification of the
individual from whom the data was
collected. Solvers are responsible for
compliance with all applicable federal,
state, local, and institutional laws,
regulations, and policy. These may
include, but are not limited to, HIPAA,
HHS Protection of Human Subjects
regulations, and FDA regulations. If
approvals (e.g., from Institutional
Review Boards) will be required to
initiate project activities in Phase 2, it
is recommended that solvers apply for
approval at or before the Phase 1
submission deadline.
The following links are intended as a
starting point for addressing regulatory
requirements, but should not be
interpreted as a complete list of
resources on these issues:
HIPAA
Main link: https://www.hhs.gov/ocr/
privacy/.
Summary of the HIPAA Privacy Rule:
https://www.hhs.gov/ocr/privacy/hipaa/
understanding/summary/.
Summary of the HIPAA Privacy Rule:
https://www.hhs.gov/ocr/privacy/hipaa/
understanding/summary/.
Summary of the HIPAA Security Rule:
https://www.hhs.gov/ocr/privacy/hipaa/
understanding/srsummary.html.
Human Subjects—HHS
Office for Human Research Protections:
https://www.hhs.gov/ohrp/.
Protection of Human Subjects Regulations:
https://www.hhs.gov/ohrp/humansubjects/
guidance/45cfr46.html.
Policy & Guidance: https://www.hhs.gov/
ohrp/policy/.
Institutional Review Boards & Assurances:
https://www.hhs.gov/ohrp/assurances/
index.html.
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Federal Register / Vol. 77, No. 110 / Thursday, June 7, 2012 / Notices
Human Subjects—FDA
Clinical Trials: https://www.fda.gov/
ScienceResearch/SpecialTopics/
RunningClinicalTrials/default.htm.
Office of Good Clinical Practice: https://
www.fda.gov/AboutFDA/CentersOffices/
OfficeofMedicalProductsandTobacco/
OfficeofScienceandHealthCoordination/
ucm2018191.
comments should be received within 30
days of this notice.
Proposed Project
Data collection for the residential care
facility and adult day service center
components of the National Study of
Long-Term Care Providers—NEW—
National Center for Health Statistics
(NCHS), Centers for Disease Control and
Prevention (CDC).
Consumer Protection—FTC
Bureau of Consumer Protection: https://
business.ftc.gov/privacy-and-security.
Authority: 15 U.S.C. 3719.
Dated: May 31, 2012.
Farzad Mostashari,
National Coordinator for Health Information
Technology.
[FR Doc. 2012–13834 Filed 6–6–12; 8:45 am]
BILLING CODE 4150–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30-Day 12–12BZ]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
chapter 35). To request a copy of these
requests, call (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, ‘‘shall collect
statistics on health resources * * *
[and] utilization of health care,
including extended care facilities, and
other institutions.’’
NCHS seeks approval to collect data
for the residential care facility (RCF)
and adult day services center (ADSC)
components of a planned new survey,
the National Study of Long-Term Care
Providers (NSLTCP). A one year
clearance is requested.
As background here are some details
on the plans for the whole study, of
which this data collection is two
components. The entire NSLTCP is
being designed to (1) Broaden NCHS’
ongoing coverage of paid, regulated
long-term care (LTC) providers; (2)
merge with existing administrative data
on LTC providers (i.e. Centers for
Medicare and Medicaid Services (CMS)
data on nursing home, home health, and
hospice care); (3) update data more
frequently on LTC providers for which
nationally representative administrative
data do not exist; and (4) enable
comparisons across LTC provider types
and monitor the supply and use of these
providers.
The data will be collected in the 50
states and the District of Columbia from
two types of LTC facilities: 11,701 RCFs
and 5,000 ADSCs. The data to be
collected from RCCs and ADSCs include
basic characteristics, services offered,
staffing, and practices of providers, as
well as distributions of the
demographics, physical functioning,
and cognitive functioning of users (RCC
residents and ADSC participants)
aggregated to the RCC/ADSC level.
Expected users of data from this
collection effort include, but are not
limited to CDC; other Department of
Health and Human Services (DHHS)
agencies, such as the Office of the
Assistant Secretary for Planning and
Evaluation and the Agency for
Healthcare Research and Quality;
provider associations, such as
LeadingAge (formerly the American
Association of Homes and Services for
the Aging), National Center for Assisted
Living, American Seniors Housing
Association, Assisted Living Federation
of America, and National Adult Day
Services Association; universities;
foundations; and other private sector
organizations, such as AARP.
Expected burden from data collection
is 30 minutes for respondents. We
estimate that 10% of RCC and ADSC
directors will be called for 15 minutes
of data retrieval when there are errors or
omissions in their returned surveys.
There is no cost to respondents other
than their time to participate. The total
estimate of annualized burden is 8,769
hours.
ESTIMATED ANNUALIZED BURDEN TABLE
Number of
respondents
Type of respondent
Form name
RCC Director ...................................................
ADSC Director ................................................
RCC and ADSC Directors ..............................
RCC Questionnaire ........................................
ADSC Questionnaire ......................................
Data Retrieval ................................................
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Kimberly S. Lane,
Deputy Director, Office of Science Integrity,
Office of the Associate Director for Science,
Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2012–13795 Filed 6–6–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Native Employment Works
(NEW) Program Plan Guidance and
Report Requirements.
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Average
burden/
response
(in hours)
Number of
responses/
respondent
11,701
5,000
1,670
1
1
1
30/60
30/60
15/60
OMB No.: 0970–0174.
Description
The Native Employment Works
(NEW) program plan is the application
for NEW program funding. As approved
by the Department of Health and Human
Services (HHS), it documents how the
grantee will carry out its NEW program.
The NEW program plan guidance
provides instructions for preparing a
NEW program plan and explains the
process for plan submission every third
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Agencies
[Federal Register Volume 77, Number 110 (Thursday, June 7, 2012)]
[Notices]
[Pages 33742-33745]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-13834]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Announcement of Requirements and Registration for ``My Air, My
Health Challenge''
AGENCY: Office of the National Coordinator for Health Information
Technology, HHS. National Institute of Environmental Health Sciences,
National Institutes of Health, HHS. Award Approving Official: Farzad
Mostashari, National Coordinator for Health Information Technology.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Environmental and public health are closely related and
complementary fields--and their future depends on a closer
understanding of those connections. New portable sensors have the
potential to transform the way we measure and interpret the influence
of pollution on health. These technologies can provide a picture that
is more detailed and more personal, with dramatic implications for
health care, air quality oversight, and individuals' control over their
own environments and health.
The U.S. Environmental Protection Agency (EPA) and U.S. Department
of Health and Human Service (HHS) [National Institute of Environmental
Health Sciences (NIEHS) and Office of the National Coordinator for
Health Information Technology (ONC)] envision a future in which
powerful, affordable, and portable sensors provide a rich awareness of
environmental quality, moment-to-moment physiological changes, and
long-term health outcomes. Health care will be connected to the whole
environment, improving diagnosis, treatment, and prevention at all
levels.
Many of the first steps toward this future have already been taken.
Prototype projects have developed portable air quality and physiologic
sensors, and experimental analysis tools for handling data that is
higher quantity, but often lower quality, than more traditional
monitoring techniques. The ``My Air, My Health Challenge'' aims to
build on this foundation. We are seeking solutions that integrate data
from portable physiological and air quality monitors, producing a
combined picture that is meaningful and usable. The statutory authority
for this challenge competition is Section 105 of the America COMPETES
Reauthorization Act of 2010 (Pub. L. 111-358) and section 103 of the
Clean Air Act, 42 U.S.C. 7403. This challenge addresses the mission of
the NIEHS to conduct and support programs with respect to factors in
the environment that affect human health, directly or indirectly. 42
U.S.C. 285.
DATES: Phase 1: Effective on June 6, 2012. Submission period ends
October 5, 2012, 11:59 p.m. et. Phase 2: Effective on November 19,
2012. Submission period ends May 19, 2013, 11:59 p.m. et.
FOR FURTHER INFORMATION CONTACT: Denice Shaw, EPA, 202-564-1108; Adam
Wong, ONC, 202-720-2866.
SUPPLEMENTARY INFORMATION:
Subject of Challenge Competition
The ``My Air, My Health Challenge'' is a multidisciplinary call to
innovators and software developers (``Solvers'') to enable near-real-
time, location-specific monitoring and reporting of air pollutants and
potentially related physiological parameters, using a personal/portable
integrated system to assess connections between the two (``sensor
systems''). The system must link air-pollutant concentrations with
physiological data, provide geocoded and time-stamped files in an easy-
to-use format, and transmit this data via existing networks to a
central data repository provided by EPA and HHS.
The challenge is structured in 2 phases:
Phase 1--Project Plan (no more than 15 pages, not including
appendices that may consist of diagrams/schematics, bibliography, and
other supplementary materials).
1. Propose a plausible link between health outcomes and airborne
pollutants (chemical species and/or particulates), and provide evidence
to support a plausible and physiologically meaningful relationship
between airborne pollutants and physiological metrics in a defined
population.
2. Propose a prototype design and development plan for an
integrated multi-sensor and data management system that may be easily
worn or carried by individuals within the defined target community/
population.
3. Conceptualize data generation, management (may include
processing & on-board storage), and transmission functionality of the
device.
4. Propose a small-scale proof-of-concept study to validate the
proposed prototype.
5. Study design process must include input from the target
community/population.
Phase 2--Proof-of-Concept Pilot Project.
6. Finalists attend an event for feedback, questions, and business/
entrepreneurial resources prepared by Challenge sponsors (EPA, HHS ONC,
NIEHS).
7. Solvers develop the proposed prototype and execute experimental
validation of the system to bring together data from personal air
quality and physiological monitors, showing how these types of data and
sensors can be integrated for practical use by health and environmental
agencies, and by individual citizens. Proof-of-concept data must
illustrate the accuracy and precision of the raw data and of any
processed data produced by the system.
Level of Focus for Health/Pollution connections: Systems must track
airborne pollutants and physiological parameters for a known or
plausible health-pollution link. Solvers must be able to justify their
chosen combination with research citations and to optimize the air
sampling parameters (volume, frequency, etc.) and physiological
measurement parameters to provide resolution appropriate to the
specific pollutant, or combination of pollutants, and related health
implications. Challenge Sponsors will provide examples of such links
for illustrative purposes (appended to the challenge announcement), but
will not limit Solvers to these particular cases.
Sensor development: Solvers are not expected to develop novel
sensors for this challenge, but are not restricted to commercially
available sensors. They may use sensors that are currently in the
development or piloting stage, but must show that the sensor will be
ready to use in functional tests--at least at a small scale--in time
for the Phase 2 proof-of-concept demonstration. Instruments must be
well characterized in terms of precision, accuracy and sensitivity.
Integrated sensor systems must be able to transmit data to the central
repository (in real time, or store and forward) using existing data
networks (e.g. 3G, LTE, or WiFi), or able to connect with personal
devices (e.g., smart phones) that have such capability. Solvers must
enable appropriate calibration and error checking capabilities,
although these need not be onboard the portable monitoring components.
Data Requirements and Constraints: Data transmitted by the
integrated devices to a centralized data repository must enable the
following to be understood from transmitted data:
1. Indicators of device functionality, including any results of
automated
[[Page 33743]]
system diagnostics, calibrations, or error logs
2. The device unique identifier, including any paired communication
device identifier (particularly important if bidirectional
communication functionality is proposed)
3. Date and time the data were collected/measurements made (start
and end timestamp)
4. The location of the device during data collection (geocode)--if
sampling occurs over several minutes or longer Solvers should consider
that users may be using transportation and that analysis should ideally
show locations between sample start and end
5. Raw measurement data (quantitative or semi-quantitative) as well
as any processed data or combined
6. Quality control metrics indicating, for instance, whether the
device is being worn/carried or functioning correctly. Error checking
can occur either prior to or after data transmission, but is an
essential component.
The preferred data transmission file format is comma separated
value (.csv) or variants thereof. Alternatively, encrypted binary files
are also acceptable. Encryption keys/codes should be provided to the
Challenge Sponsors so that data can be accessed at the central data
repository.
Pollutant Focus: Solvers will be required to include at least one
air pollution metric--although at their discretion they may include
multiple air pollution metrics and/or other environmental metrics such
as noise level and UV exposure. The focus, however, will be on chemical
and/or particulate air pollutants.
Physiological Parameter Focus: Solvers will be required to include
at least one physiological metric--although at their discretion they
may include multiple physiological metrics and/or other person-oriented
metrics such as behaviors and social interactions. The focus, however,
will be on physical parameters (e.g., heart rate, breathing, pulse
oxygenation), and their connection to pollutants.
Physical Guidelines for Sensors: At least one component of the
sensor system must be wearable or carryable, and all components should
have a minimal burden and be minimally obtrusive. The overall sensor
system must focus on personal and local metrics (i.e., measuring air
quality in the immediate vicinity of the wearer). Wearable components
must be the right size and weight for their target audience (e.g., no
more than 300 g for a child). Sampling frequency and area must be
appropriate to the pollutants and physiological metrics of interest, as
well as to the context of data collection (e.g., by walkers, cyclists
or passengers on public transportation). The sensor system must include
an on-board data buffer for when network access is unavailable, and may
also at the Solver's discretion include personal media to which data
may be downloaded for permanent or temporary storage. Open source
hardware and software are desired but not required.
Measurement Guidelines for Sensors: Accuracy, detection limit,
measurement range, and sensitivity of all sensors must be at sufficient
resolution to record health-relevant changes in air pollutant(s) and
physiological marker(s). If processing of the data is required in order
to achieve this (e.g., normalization, increasing signal-to-noise
ratios), the Solver must include the algorithm and its scientific basis
(i.e., previously collected data and/or appropriate citations) in their
report. Alternatively, centralized processing that enables parsing of
local data, in order to increase data robustness and reduce false
positive signals, may be used. If such an approach is determined to be
useful, Solvers must outline suitable strategies and/or boundary
criteria. In either case, solvers must communicate the overall
uncertainty level of the final system output
Community Involvement: The sensor system must address a need in a
specific community or population. In addition to scientific evidence
supporting that need, Solvers must also seek and document community
input. Representatives of the affected community should provide
feedback on the pilot project both during conceptualization (Phase 1),
and throughout the pilot study (Phase 2). This is not intended to
override the Solvers' scientific judgment on technical issues, but to
ensure that the project is respectful of local knowledge, community
identity, and needs. Projects must include feedback to the community
regarding both technical success (e.g., whether sensors performed as
planned) and results (e.g., any correlations found in the data).
Scaling and Future Plans: While Phase 2 requires only a small-scale
proof-of-concept project, final submissions for this phase must include
a description of how the project could or will be extended and
expanded. In general, Solvers are asked to propose concrete next steps
that might be carried out with more time or resources available.
Eligibility Rules for Participating in the Competition
To be eligible to win a prize under this challenge, an individual
or entity shall have complied with all the requirements under this
section and Federal Register Notice.
This challenge is open to any Solver who is (1) an individual or
team of U.S. citizens or permanent residents of the United States who
are 18 years of age and over, or (2) an entity incorporated in and
maintaining a primary place of business in the United States. Foreign
citizens can participate as employees of an entity that is properly
incorporated in the U.S. and maintains a primary place of business in
the U.S. Solvers may submit more than one entry.
Eligibility for Phase 2 is conditional upon being selected as a
Phase 1 Finalist. Eligibility for a prize award is contingent upon
fulfilling all requirements set forth herein. An individual, team, or
entity that is currently on the Excluded Parties List (https://www.epls.gov/) will not be selected as a Finalist or Winner.
Employees of EPA, HHS, and the reviewers or any other company or
individual involved with the design, production, execution, or
distribution of the challenge and their immediate family (spouse,
parents and step-parents, siblings and step-siblings, and children and
step-children) and household members (people who share the same
residence at least three (3) months out of the year) are not eligible
to participate.
An individual or entity may not be a Federal entity or Federal
employee acting within the scope of their employment. Federal employees
seeking to participate in this challenge outside the scope of their
employment should consult their ethics official prior to developing a
submission. An individual or entity shall not be deemed ineligible
because the individual or entity used Federal facilities or consulted
with Federal employees during a competition if the facilities and
employees are made available to all individuals and entities
participating in the competition on an equitable basis.
Federal grantees may not use Federal funds to develop COMPETES Act
challenge applications unless consistent with the purpose of their
grant award. (Grantees should consult with their cognizant Grants
Management Official to make this determination.) Federal contractors
may not use Federal funds from a contract to develop COMPETES Act
challenge applications or to fund efforts in support of a COMPETES Act
challenge submission.
[[Page 33744]]
Liability and Indemnification: By participating in this
competition, Solvers agree to assume any and all risks and waive claims
against the Federal Government and its related entities, except in the
case of willful misconduct, for any injury, death, damage, or loss of
property, revenue, or profits, whether direct, indirect, or
consequential, arising from participation in this competition, whether
the injury, death, damage, or loss arises through negligence or
otherwise. By participating in this competition, Solvers agree to
indemnify the Federal Government against third party claims for damages
arising from or related to competition activities.
Insurance: Based on the subject matter of the competition, the type
of work that it will possibly require, as well as an analysis of the
likelihood of any claims for death, bodily injury, or property damage,
or loss potentially resulting from competition participation, Solvers
are not required to obtain liability insurance or demonstrate financial
responsibility in order to participate in this competition.
Registration Process for Participants
To register for this challenge participants may do any of the
following:
[ssquf] Access the www.challenge.gov Web site and search for the
``My Air, My Health Challenge''.
[ssquf] Access the ONC Investing in Innovation (i2) Challenge Web
site at:
[cir] https://www.health2con.com/devchallenge/challenges/onc-i2-challenges/.
[cir] A registration link for the challenge can be found on the
landing page under the challenge description.
[ssquf] Access the Innocentive challenge Web site at
www.innocentive.com/myairmyhealth.
Amount of the Prize
[ssquf] Phase 1: $15,000 each for up to four Finalists who are
selected to move on to Phase 2.
[ssquf] Phase 2: $100,000 to the Winner.
Awards may be subject to Federal income taxes.
Payment of the Prize
HHS and EPA prizes awarded under this competition will be paid by
electronic funds transfer and may be subject to Federal income taxes.
HHS and EPA will comply with the Internal Revenue Service withholding
and reporting requirements, where applicable.
Basis Upon Which Winner Will Be Selected
The review panel will make selections based upon the following
criteria in Phase 1:
[ssquf] Strength of evidence and/or argumentation regarding the
linkage between air pollutant and physiological effect.
[ssquf] Potential significance of technology and eventual benefit
to target population(s).
[ssquf] Viability of proposed sensor technologies to detect and
quantify pollutants and their effects, and provide physiologically
relevant health and air quality data.
[ssquf] Viability of the proposed data reporting technology
(communication to a centralized data repository provided by EPA and
HHS)
[ssquf] Viability of the proposed project plan.
[ssquf] Viability of the proposed instrument design as a wearable/
portable device.
[ssquf] Viability of the proposed proof-of-concept study (low
complexity is preferred).
[ssquf] Appropriate use of community input in designing proof-of-
concept study.
The review panel will make selections based upon the following
criteria in Phase 2:
[ssquf] Sensors: Successful technical collection of both health and
environmental data
[ssquf] Data Reporting: Successful formatting and transmission of
data
[ssquf] Data processing and evaluation
[ssquf] Community Involvement and Interaction
Additional Information
Intellectual Property Rights: Upon submission, each Solver warrants
that he or she is the sole author and owner of the work, that the work
is wholly original with the Solver (or is an improved version of an
existing work that the Solver has sufficient rights to use--including
the substantial improvement of existing open-source work) and that it
does not infringe any copyright or any other rights of any third party
of which Solver is aware. Each Solver also warrants that the work is
free of malware.
(a) Copyright. By participating in this competition, each Solver
hereby grants to the Federal government an irrevocable, paid-up,
royalty-free, nonexclusive worldwide license to reproduce, distribute
copies, display, create derivative works, and publicly post, link to,
and share, the work or parts thereof, including any parts for which it
has obtained rights from a third party, in any medium, for Federal
purposes. User warrants that it has obtained rights to any parts of the
work not authored by Solver adequate to convey the aforementioned
license. (b) Inventions. Finalists hereby grant to the Federal
government a nonexclusive, nontransferable, irrevocable, paid-up
license to practice or have practiced for or on behalf of the United
States any invention throughout the world made by Finalists that, if
patented, would cover the submission or its use.
Privacy, Data Security, Ethics, and Compliance
Solvers are required to identify and address privacy and security
issues in their proposed projects, and describe specific solutions for
meeting them.
In addition to complying with appropriate policies, procedures, and
protections for data that ensures all privacy requirements and
institutional policies are met, use of data should not allow the
identification of the individual from whom the data was collected.
Solvers are responsible for compliance with all applicable federal,
state, local, and institutional laws, regulations, and policy. These
may include, but are not limited to, HIPAA, HHS Protection of Human
Subjects regulations, and FDA regulations. If approvals (e.g., from
Institutional Review Boards) will be required to initiate project
activities in Phase 2, it is recommended that solvers apply for
approval at or before the Phase 1 submission deadline.
The following links are intended as a starting point for addressing
regulatory requirements, but should not be interpreted as a complete
list of resources on these issues:
HIPAA
Main link: https://www.hhs.gov/ocr/privacy/.
Summary of the HIPAA Privacy Rule: https://www.hhs.gov/ocr/privacy/hipaa/understanding/summary/.
Summary of the HIPAA Privacy Rule: https://www.hhs.gov/ocr/privacy/hipaa/understanding/summary/.
Summary of the HIPAA Security Rule: https://www.hhs.gov/ocr/privacy/hipaa/understanding/srsummary.html.
Human Subjects--HHS
Office for Human Research Protections: https://www.hhs.gov/ohrp/.
Protection of Human Subjects Regulations: https://www.hhs.gov/ohrp/humansubjects/guidance/45cfr46.html.
Policy & Guidance: https://www.hhs.gov/ohrp/policy/.
Institutional Review Boards & Assurances: https://www.hhs.gov/ohrp/assurances/.
[[Page 33745]]
Human Subjects--FDA
Clinical Trials: https://www.fda.gov/ScienceResearch/SpecialTopics/RunningClinicalTrials/default.htm.
Office of Good Clinical Practice: https://www.fda.gov/AboutFDA/CentersOffices/OfficeofMedicalProductsandTobacco/OfficeofScienceandHealthCoordination/ucm2018191.
Consumer Protection--FTC
Bureau of Consumer Protection: https://business.ftc.gov/privacy-and-security.
Authority: 15 U.S.C. 3719.
Dated: May 31, 2012.
Farzad Mostashari,
National Coordinator for Health Information Technology.
[FR Doc. 2012-13834 Filed 6-6-12; 8:45 am]
BILLING CODE 4150-45-P