Office of the National Coordinator for Health Information Technology; Announcement of Requirements and Registration for “EHR Innovations for Improving Hypertension Challenge”, 38895-38897 [2014-16016]
Download as PDF
Federal Register / Vol. 79, No. 131 / Wednesday, July 9, 2014 / Notices
2011. No public comments were
received in prior years that have
challenged the validity of the
Government’s estimate.
Respondents: 949.
Responses per Respondent: 1.
Hours per Response: 0.325.
Total Burden Hours: 308.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat Division (MVCB),
1800 F Street NW., Washington, DC
20405, telephone 202–501–4755.
Please cite OMB Control No. 9000–
0155, Prohibition on Acquisition of
Products Produced by Forced or
Indentured Child Labor, in all
correspondence.
Dated: July 2, 2014.
Karlos Morgan,
Acting Director, Federal Acquisition Policy
Division, Office of Government-Wide
Acquisition Policy, Office of Acquisition
Policy, Office of Government-Wide Policy.
[FR Doc. 2014–16081 Filed 7–8–14; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency Information Collection
Activities: Proposed Collection; 30-Day
Public Comment Request;
Communications Testing for
Comprehensive Communication
Campaign for HITECH ACT
Office of the National
Coordinator for Health Information
Technology, Department of Health and
Human Services.
ACTION: 30-Day notice of submission of
information collection approval from
the Office of Management and Budget
and request for comments.
AGENCY:
In compliance with section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the
National Coordinator for Health
Information Technology (ONC),
Department of Health and Human
Services, announces plans to submit an
Information Collection Request (ICR),
described below, to the Office of
Management and Budget (OMB). The
ICR is for extending the use of the
approved information collection
assigned OMB control number 0955–
0005, which expires on July 31, 2014.
Prior to submitting that ICR to OMB,
ONC seeks comments from the public
regarding the burden estimate, below, or
any other aspect of the ICR.
DATES: Comments must be submitted by
August 8, 2014.
sroberts on DSK5SPTVN1PROD with NOTICES
SUMMARY:
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Written comments may be
submitted to
Information.CollectionClearance@
hhs.gov or by calling (202) 690–6162.
FOR FURTHER INFORMATION CONTACT: To
request additional information, please
contact Penelope Hughes at
Penelope.Hughes@hhs.gov or (202)
205.8658.
ADDRESSES:
SUPPLEMENTARY INFORMATION:
Title: ‘‘Communications Testing for
Comprehensive Communication
Campaign for HITECH ACT.’’
Abstract: The Office of the National
Coordinator for Health Information
Technology (ONC) serves as the Health
and Human Services (HHS) Secretary’s
principal advisor on the development,
application, and use of health
information technology (health IT). ONC
is requesting an approval by OMB on an
extension, to a previously approved
generic clearance titled
Communications Testing for
Comprehensive Communication
Campaign for HITECH ACT, 0955–0005,
for collecting information through a
variety of research methods for the
purpose of developing and testing
communications involving health
information technology and health
information privacy. ONC
responsibilities include promoting the
development of a nationwide health IT
infrastructure that allows for electronic
use and exchange of information and
fostering the public understanding of
health information technology,
including educating the public about
health information privacy. In order to
fulfill these responsibilities, information
from the public at large is necessary to
determine what education is needed
and what types of communication
techniques will be most effective. Due to
the rapidly evolving nature of health
information technology, an extension of
the original generic data collection is
being requested to ensure that these
education and communication efforts
keep pace with technological
advancements and the changing health
information technology ecosystem. This
information will be used to assess the
need for communications on specific
topics and to assist in the development
and modification of communication
messages. The data will help in tailoring
print, broadcast, and electronic media
communications and other materials for
them to have powerful and desired
impacts on target audiences. The data
will not be used for the purposes of
making policy or regulatory decisions.
The agency received no comments in
response to the 60-day notice for the
extension request published in the
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Sfmt 4703
38895
Federal Register of April 3, 2014 (79 FR
18690).
Below we provide the Office of the
National Coordinator for Health
Information Technology’s projected
average estimates for the next three
years: 1
Current Actions: New collection of
information.
Type of Review: Extension.
Affected Public: Likely respondents
include consumers as well as
physicians, nurses and other health care
providers.
Average Expected Annual Number of
Activities: 6.
Respondents: 1,900.
Annual Responses: 11,400.
Frequency of Response: Once per
request.
Average Minutes per Response: 15.
Burden Hours: 2850.
An agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid
Office of Management and Budget
control number.
Darius Taylor,
Information Collections Clearance Officer.
[FR Doc. 2014–16022 Filed 7–8–14; 8:45 am]
BILLING CODE 4150–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the National Coordinator for
Health Information Technology;
Announcement of Requirements and
Registration for ‘‘EHR Innovations for
Improving Hypertension Challenge’’
Office of the National
Coordinator for Health Information
Technology, HHS.
Award Approving Official: Karen
DeSalvo, National Coordinator for
Health Information Technology.
ACTION: Notice.
AGENCY:
The goal of the EHR
Innovations for Improving Hypertension
Challenge is to seek practices that have
used clinical decision support (CDS) to
implement the most clinically
successful examples of an evidencebased blood pressure treatment
protocol, gather details about these tools
SUMMARY:
1 The 60-day notice included the following
estimate of the aggregate burden hours for this
generic clearance federal-wide:
Average Expected Annual Number of activities: 6.
Average Number of Respondents per Activity:
1,900.
Annual Responses: 11,400.
Frequency of Response: Once per request.
Average Minutes per Response: 12.
Burden Hours: 2,300.
E:\FR\FM\09JYN1.SGM
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38896
Federal Register / Vol. 79, No. 131 / Wednesday, July 9, 2014 / Notices
and their implementation, and then
drive widespread implementation of
those tools by other providers. In Phase
1 (three months), practices will
document the CDS tools they used to
implement an evidence-based BP
control protocol, as well as describe the
details and results of the
implementation. Practices must
demonstrate high BP control levels and/
or improvement to ensure that tools and
strategies merit replication across
practice settings. In Phase 2 (nine
months), practices and their partners
will conduct, evaluate and document
dissemination strategies for tools
identified in Phase 1, emphasizing
widespread, effective use of these tools
by other practices. Submitters must
demonstrate successful use of these
tools in at least 2 additional practices.
The statutory authority for this
challenge competition is Section 105 of
the America COMPETES
Reauthorization Act of 2010 (Public L.
No 111–358).
DATES:
• Phase I submission period: July 7–
October 6, 2014.
• Phase I winners announcement,
tools posted: October 27, 2014.
• Phase II submission period: October
28, 2014–July 31, 2015.
• Phase II winners announcement:
August/September, 2015.
FOR FURTHER INFORMATION CONTACT:
Adam Wong, adam.wong@hhs.gov
(preferred), 202–720–2866.
SUPPLEMENTARY INFORMATION:
sroberts on DSK5SPTVN1PROD with NOTICES
Subject of Challenge Competition
Phase 1 Details
1. Purpose: Identify CDS tools and
approaches effectively used by
individual practices to improve blood
pressure so they can be spread to other
practices.
2. Participants: A practice
implementing the protocol must lead
the submission. Practices are
encouraged to form teams supporting
their entry that include organizations
such as a Regional Extension Center
(REC), EHR developer, quality
organization and/or professional
society.
3. Duration: 3 months.
4. Required to submit:
a. Provide data on BP control rate
and/or improvement, as well as data on
hypertension prevalence in the practice
(prevalence data is collected to better
understand the organization’s
hypertension screening results, but is
not used for review)
• Submission requires more than
70% BP control (<140/90) in
hypertension patients; specifications
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20:08 Jul 08, 2014
Jkt 232001
used to determine this rate must be the
same as that used for PQRS #236/NQF
#0018 and/or
• Significant improvement over time
in BP control: Provide the percent of the
patient population whose BP rate was
improved over a specified period. Each
submission will be evaluated based on
the percent improvement and time
period but no specific threshold for
these must be met as a part of
submission requirements.
• Information about the patients
affected by the CDS interventions to
help describe the Challenge’s reach and
effects, including: Size of the practice’s
patient population and hypertension
prevalence; Aggregate demographic
information on the patient population
(e.g., disparities); and Specialty and
demographic information about the
practice (e.g., number/type of providers,
setting [rural vs. urban], type [academic
vs. community]).
b. Describe Protocol elements
addressed (use structured narrative; we
encourage but do not require that
submitters address all five elements):
• BP measurement/recording (e.g.,
use of documentation templates,
highlighting abnormal BPs in EHR).
• BP follow-up and patient recall
(e.g., use of registry reports).
• Medication selection and titration
(e.g., use of order sets).
• Patient engagement (e.g., use of
patient education and goal setting tools,
templates for documenting and
responding to home BP readings, patient
reminders for medications/
appointments).
• Workup/referral for poor control
(e.g., reference information,
hypertension-specific consult order
forms).
c. Describe EHR/health IT tools used
to implement protocol (generic
description; screenshots optional) and
details about deployment so that others
can replicate it.
• Order sets, registry reports,
documentation templates/tools,
medication protocols, patient
engagement/education tools, referral
templates, reminders, etc.
• Tool descriptions can include
generic version of intervention (e.g.,
contents of order set, documentation
template, rule), screenshots, and/or
implementable artifacts. We encourage,
but do not require, use of the format
described in the HL7 CDS Knowledge
sharing implementation guide (also
called the ‘Health eDecisions’ format).
d. Describe how the tools are
deployed in workflow.
• Use CDS/Quality Improvement
worksheets for standard presentation/
replication (e.g., similar to QI case
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
example within the CDS/QI resources
recently provided by ONC 1).
Phase 2 Details
1. Purpose:
• The ultimate goal is that many
organizations (e.g., professional
societies, developers, quality
organizations, RECs) spread use of the
effective tools and related workflows
from Phase 1 to many additional
practice settings.
• Phase 2 submitters will develop and
implement strategies for disseminating
the CDS interventions recognized from
Phase 1 as having the greatest value for
BP control.
• Organizations with the greatest
spread results and further spread
potential will be selected for
recognition, including a single winner,
from the Phase 2 Challenge component.
2. Participants: Phase 2 Challenge
applicants can include any organization
or collaboration that is able to widely
spread successful use of EHR/CDSenabled BP treatment protocols using
tools recognized during Phase 1. Phase
2 submitters need not have participated
in Phase 1.2
3. Duration: 9 months.
4. Required to submit:
a. Evidence that the tools and artifacts
were implemented, or implementation
is underway, in at least 2 other practices
or provider groups.
• As part of describing the spread
strategy, submitters must describe the
CDS tools that were used to implement
the hypertension control protocol; the
format for this is based on that from
Phase 1, and also includes any
modification made to the tools so they
could spread. We encourage, but do not
require, use of the format described in
the HL7 CDS Knowledge Sharing
Implementation Guide (i.e., the ‘Health
eDecisions’ format).
b. Results from spreading CDS tools to
other practices: Ideally blood pressure
control/improvements similar to that
achieved from the tools in Phase 1, but,
at a minimum, compelling evidence of
significant value from tool
implementation.
c. Evidence of intent from other
practices (i.e., in addition to those
practices covered in 4.a above) to
replicate the BP protocol approach
using the CDS tools.
1 These resources are available at: bit.ly/CDS4MU;
see specifically II.A: CHC Inc. and Ellsworth QI
Case Studies.
2 Phase 2 success will likely require partnership
with organizations that have significant size and
reach—such as specialty societies, quality
organizations, RECs, health IT products or services
vendors—to support tool dissemination goals.
E:\FR\FM\09JYN1.SGM
09JYN1
Federal Register / Vol. 79, No. 131 / Wednesday, July 9, 2014 / Notices
sroberts on DSK5SPTVN1PROD with NOTICES
d. Information about the patients
affected by the CDS interventions,
including:
• Size of practice’s patient population
and hypertension prevalence;
• Aggregate demographic information
on the patient population (i.e.,
disparities); and
• Specialty and demographic
information about the practice (e.g.,
number of providers, setting [rural vs.
urban], type [academic vs. community]).
This information will help define the
Challenge’s reach and effects; the
Challenge is intended to affect many
different practices sizes and types.
e. Practice deployment strategy
summary and critical success factors for
spreading CDS tool implementation to
enhance BP control.
Eligibility Rules for Participating in the
Competition
To be eligible to win a prize under
this challenge, an individual or entity—
(1) Shall have registered to participate
in the competition under the rules
promulgated by the Office of the
National Coordinator for Health
Information Technology.
(2) Shall have complied with all the
requirements under this section.
(3) In the case of a private entity, shall
be incorporated in and maintain a
primary place of business in the United
States, and in the case of an individual,
whether participating singly or in a
group, shall be a citizen or permanent
resident of the United States.
(4) May not be a Federal entity or
Federal employee acting within the
scope of their employment.
(5) Shall not be an HHS employee
working on their applications or
submissions during assigned duty
hours.
(6) Shall not be an employee of Office
of the National Coordinator for Health
IT.
(7) Federal grantees may not use
Federal funds to develop COMPETES
Act challenge applications unless
consistent with the purpose of their
grant award.
(8) 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.
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.
Entrants must agree to assume any
and all risks and waive claims against
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20:08 Jul 08, 2014
Jkt 232001
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 my
participation in this prize contest,
whether the injury, death, damage, or
loss arises through negligence or
otherwise.
Entrants must also agree to indemnify
the Federal Government against third
party claims for damages arising from or
related to competition activities.
Registration Process for Participants
To register for this Challenge,
participants can access https://
www.challenge.gov and search for ‘‘EHR
Innovations for Improving Hypertension
Challenge.’’
Prize
Phase 1 will have up to 4 winners,
each of whom will receive a $5,000
prize. Other Phase 1 submitters who
provide CDS tools that reviewers select
for spread during Phase 2 dissemination
efforts will receive non-monetary
recognition (e.g., Honorable Mention).
Phase 2 will have a single winner of
a $30,000 cash prize. Other Phase 2
submitters, whose CDS tool
dissemination and implementation
strategies the reviewers deem
commendable, will receive nonmonetary recognition (e.g., Honorable
Mention).
Payment of the Prize
Prize will be paid by contractor.
Basis Upon Which Winner Will Be
Selected
The review panel will make selections
based upon the following criteria:
Phase 1
• BP Control (<140/90) among
hypertension patients.
Æ BP control rate: Specifications used
to determine this rate must be the same
as that used for PQRS #236/NQF #0018)
and/or
Æ BP control rate improvement:
Percentage point increase in BP control
rate over a specified time. Submissions
will be evaluated based on the percent
improvement, if this is provided by
submitters, but no specific threshold
must be demonstrated as a part of
submission requirements.
• Comprehensiveness and innovation
in addressing the protocol elements
using EHR or other health IT.
• CDS tool implementation
description detailed enough so that
others could replicate it.
• Ease with which others could
implement the same approach (e.g., if
PO 00000
Frm 00048
Fmt 4703
Sfmt 9990
38897
the strategy required a high degree of
custom development that cannot easily
be shared, then it would be harder for
others to replicate).
Phase 2
• Number of practices in which the
CDS interventions were implemented,
or implementation is underway.
• Number of practices expressing
interest in replicating the CDS-enabled
protocol implementation approach in
addition to those that actually
implemented it during Phase 2.
• CDS tool implementation spread
efforts resulting in demonstrated BP
control improvements. Absent actual BP
control improvements, demonstration of
compelling evidence that CDS tool
implementation has made a positive
impact on BP care processes and/or that
BP control improvements are likely.
• Comprehensiveness and innovation
in supporting BP protocol elements with
CDS tools.
• Likelihood that the submitter’s
approach to spreading the CDS toolenabled BP protocol implementation
can be further replicated beyond Phase
2.
In order for an entry to be eligible to
win this Challenge, it must not use
HHS’ or ONC’s logos or official seals in
the Submission, and must not claim
endorsement.
Additional Information
General Conditions: ONC reserves the
right to cancel, suspend, and/or modify
the Contest, or any part of it, for any
reason, at ONC’s sole discretion.
Intellectual Property:
• Each entrant retains title and full
ownership in and to their submission.
Entrants expressly reserve all
intellectual property rights not
expressly granted under the challenge
agreement.
• By participating in the challenge,
each entrant hereby irrevocably grants
to Sponsor and Administrator a limited,
non-exclusive, royalty-free, worldwide
license and right to reproduce,
publically perform, publically display,
and use the Submission to the extent
necessary to administer the challenge,
and to publically perform and
publically display the Submission,
including, without limitation, for
advertising and promotional purposes
relating to the challenge.
Authority: 15 U.S.C. 3719.
Dated: June 26, 2014.
Karen DeSalvo,
National Coordinator for Health Information
Technology.
[FR Doc. 2014–16016 Filed 7–7–14; 8:45 am]
BILLING CODE 4150–45–P
E:\FR\FM\09JYN1.SGM
09JYN1
Agencies
[Federal Register Volume 79, Number 131 (Wednesday, July 9, 2014)]
[Notices]
[Pages 38895-38897]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-16016]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the National Coordinator for Health Information
Technology; Announcement of Requirements and Registration for ``EHR
Innovations for Improving Hypertension Challenge''
AGENCY: Office of the National Coordinator for Health Information
Technology, HHS.
Award Approving Official: Karen DeSalvo, National Coordinator for
Health Information Technology.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The goal of the EHR Innovations for Improving Hypertension
Challenge is to seek practices that have used clinical decision support
(CDS) to implement the most clinically successful examples of an
evidence-based blood pressure treatment protocol, gather details about
these tools
[[Page 38896]]
and their implementation, and then drive widespread implementation of
those tools by other providers. In Phase 1 (three months), practices
will document the CDS tools they used to implement an evidence-based BP
control protocol, as well as describe the details and results of the
implementation. Practices must demonstrate high BP control levels and/
or improvement to ensure that tools and strategies merit replication
across practice settings. In Phase 2 (nine months), practices and their
partners will conduct, evaluate and document dissemination strategies
for tools identified in Phase 1, emphasizing widespread, effective use
of these tools by other practices. Submitters must demonstrate
successful use of these tools in at least 2 additional practices.
The statutory authority for this challenge competition is Section
105 of the America COMPETES Reauthorization Act of 2010 (Public L. No
111-358).
DATES:
Phase I submission period: July 7-October 6, 2014.
Phase I winners announcement, tools posted: October 27,
2014.
Phase II submission period: October 28, 2014-July 31,
2015.
Phase II winners announcement: August/September, 2015.
FOR FURTHER INFORMATION CONTACT: Adam Wong, adam.wong@hhs.gov
(preferred), 202-720-2866.
SUPPLEMENTARY INFORMATION:
Subject of Challenge Competition
Phase 1 Details
1. Purpose: Identify CDS tools and approaches effectively used by
individual practices to improve blood pressure so they can be spread to
other practices.
2. Participants: A practice implementing the protocol must lead the
submission. Practices are encouraged to form teams supporting their
entry that include organizations such as a Regional Extension Center
(REC), EHR developer, quality organization and/or professional society.
3. Duration: 3 months.
4. Required to submit:
a. Provide data on BP control rate and/or improvement, as well as
data on hypertension prevalence in the practice (prevalence data is
collected to better understand the organization's hypertension
screening results, but is not used for review)
Submission requires more than 70% BP control (<140/90) in
hypertension patients; specifications used to determine this rate must
be the same as that used for PQRS 236/NQF 0018 and/or
Significant improvement over time in BP control: Provide
the percent of the patient population whose BP rate was improved over a
specified period. Each submission will be evaluated based on the
percent improvement and time period but no specific threshold for these
must be met as a part of submission requirements.
Information about the patients affected by the CDS
interventions to help describe the Challenge's reach and effects,
including: Size of the practice's patient population and hypertension
prevalence; Aggregate demographic information on the patient population
(e.g., disparities); and Specialty and demographic information about
the practice (e.g., number/type of providers, setting [rural vs.
urban], type [academic vs. community]).
b. Describe Protocol elements addressed (use structured narrative;
we encourage but do not require that submitters address all five
elements):
BP measurement/recording (e.g., use of documentation
templates, highlighting abnormal BPs in EHR).
BP follow-up and patient recall (e.g., use of registry
reports).
Medication selection and titration (e.g., use of order
sets).
Patient engagement (e.g., use of patient education and
goal setting tools, templates for documenting and responding to home BP
readings, patient reminders for medications/appointments).
Workup/referral for poor control (e.g., reference
information, hypertension-specific consult order forms).
c. Describe EHR/health IT tools used to implement protocol (generic
description; screenshots optional) and details about deployment so that
others can replicate it.
Order sets, registry reports, documentation templates/
tools, medication protocols, patient engagement/education tools,
referral templates, reminders, etc.
Tool descriptions can include generic version of
intervention (e.g., contents of order set, documentation template,
rule), screenshots, and/or implementable artifacts. We encourage, but
do not require, use of the format described in the HL7 CDS Knowledge
sharing implementation guide (also called the `Health eDecisions'
format).
d. Describe how the tools are deployed in workflow.
Use CDS/Quality Improvement worksheets for standard
presentation/replication (e.g., similar to QI case example within the
CDS/QI resources recently provided by ONC \1\).
---------------------------------------------------------------------------
\1\ These resources are available at: bit.ly/CDS4MU; see
specifically II.A: CHC Inc. and Ellsworth QI Case Studies.
---------------------------------------------------------------------------
Phase 2 Details
1. Purpose:
The ultimate goal is that many organizations (e.g.,
professional societies, developers, quality organizations, RECs) spread
use of the effective tools and related workflows from Phase 1 to many
additional practice settings.
Phase 2 submitters will develop and implement strategies
for disseminating the CDS interventions recognized from Phase 1 as
having the greatest value for BP control.
Organizations with the greatest spread results and further
spread potential will be selected for recognition, including a single
winner, from the Phase 2 Challenge component.
2. Participants: Phase 2 Challenge applicants can include any
organization or collaboration that is able to widely spread successful
use of EHR/CDS-enabled BP treatment protocols using tools recognized
during Phase 1. Phase 2 submitters need not have participated in Phase
1.\2\
---------------------------------------------------------------------------
\2\ Phase 2 success will likely require partnership with
organizations that have significant size and reach--such as
specialty societies, quality organizations, RECs, health IT products
or services vendors--to support tool dissemination goals.
---------------------------------------------------------------------------
3. Duration: 9 months.
4. Required to submit:
a. Evidence that the tools and artifacts were implemented, or
implementation is underway, in at least 2 other practices or provider
groups.
As part of describing the spread strategy, submitters must
describe the CDS tools that were used to implement the hypertension
control protocol; the format for this is based on that from Phase 1,
and also includes any modification made to the tools so they could
spread. We encourage, but do not require, use of the format described
in the HL7 CDS Knowledge Sharing Implementation Guide (i.e., the
`Health eDecisions' format).
b. Results from spreading CDS tools to other practices: Ideally
blood pressure control/improvements similar to that achieved from the
tools in Phase 1, but, at a minimum, compelling evidence of significant
value from tool implementation.
c. Evidence of intent from other practices (i.e., in addition to
those practices covered in 4.a above) to replicate the BP protocol
approach using the CDS tools.
[[Page 38897]]
d. Information about the patients affected by the CDS
interventions, including:
Size of practice's patient population and hypertension
prevalence;
Aggregate demographic information on the patient
population (i.e., disparities); and
Specialty and demographic information about the practice
(e.g., number of providers, setting [rural vs. urban], type [academic
vs. community]).
This information will help define the Challenge's reach and
effects; the Challenge is intended to affect many different practices
sizes and types.
e. Practice deployment strategy summary and critical success
factors for spreading CDS tool implementation to enhance BP control.
Eligibility Rules for Participating in the Competition
To be eligible to win a prize under this challenge, an individual
or entity--
(1) Shall have registered to participate in the competition under
the rules promulgated by the Office of the National Coordinator for
Health Information Technology.
(2) Shall have complied with all the requirements under this
section.
(3) In the case of a private entity, shall be incorporated in and
maintain a primary place of business in the United States, and in the
case of an individual, whether participating singly or in a group,
shall be a citizen or permanent resident of the United States.
(4) May not be a Federal entity or Federal employee acting within
the scope of their employment.
(5) Shall not be an HHS employee working on their applications or
submissions during assigned duty hours.
(6) Shall not be an employee of Office of the National Coordinator
for Health IT.
(7) Federal grantees may not use Federal funds to develop COMPETES
Act challenge applications unless consistent with the purpose of their
grant award.
(8) 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.
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.
Entrants must 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 my participation in this prize contest,
whether the injury, death, damage, or loss arises through negligence or
otherwise.
Entrants must also agree to indemnify the Federal Government
against third party claims for damages arising from or related to
competition activities.
Registration Process for Participants
To register for this Challenge, participants can access https://www.challenge.gov and search for ``EHR Innovations for Improving
Hypertension Challenge.''
Prize
Phase 1 will have up to 4 winners, each of whom will receive a
$5,000 prize. Other Phase 1 submitters who provide CDS tools that
reviewers select for spread during Phase 2 dissemination efforts will
receive non-monetary recognition (e.g., Honorable Mention).
Phase 2 will have a single winner of a $30,000 cash prize. Other
Phase 2 submitters, whose CDS tool dissemination and implementation
strategies the reviewers deem commendable, will receive non-monetary
recognition (e.g., Honorable Mention).
Payment of the Prize
Prize will be paid by contractor.
Basis Upon Which Winner Will Be Selected
The review panel will make selections based upon the following
criteria:
Phase 1
BP Control (<140/90) among hypertension patients.
[cir] BP control rate: Specifications used to determine this rate
must be the same as that used for PQRS 236/NQF 0018)
and/or
[cir] BP control rate improvement: Percentage point increase in BP
control rate over a specified time. Submissions will be evaluated based
on the percent improvement, if this is provided by submitters, but no
specific threshold must be demonstrated as a part of submission
requirements.
Comprehensiveness and innovation in addressing the
protocol elements using EHR or other health IT.
CDS tool implementation description detailed enough so
that others could replicate it.
Ease with which others could implement the same approach
(e.g., if the strategy required a high degree of custom development
that cannot easily be shared, then it would be harder for others to
replicate).
Phase 2
Number of practices in which the CDS interventions were
implemented, or implementation is underway.
Number of practices expressing interest in replicating the
CDS-enabled protocol implementation approach in addition to those that
actually implemented it during Phase 2.
CDS tool implementation spread efforts resulting in
demonstrated BP control improvements. Absent actual BP control
improvements, demonstration of compelling evidence that CDS tool
implementation has made a positive impact on BP care processes and/or
that BP control improvements are likely.
Comprehensiveness and innovation in supporting BP protocol
elements with CDS tools.
Likelihood that the submitter's approach to spreading the
CDS tool-enabled BP protocol implementation can be further replicated
beyond Phase 2.
In order for an entry to be eligible to win this Challenge, it must
not use HHS' or ONC's logos or official seals in the Submission, and
must not claim endorsement.
Additional Information
General Conditions: ONC reserves the right to cancel, suspend, and/
or modify the Contest, or any part of it, for any reason, at ONC's sole
discretion.
Intellectual Property:
Each entrant retains title and full ownership in and to
their submission. Entrants expressly reserve all intellectual property
rights not expressly granted under the challenge agreement.
By participating in the challenge, each entrant hereby
irrevocably grants to Sponsor and Administrator a limited, non-
exclusive, royalty-free, worldwide license and right to reproduce,
publically perform, publically display, and use the Submission to the
extent necessary to administer the challenge, and to publically perform
and publically display the Submission, including, without limitation,
for advertising and promotional purposes relating to the challenge.
Authority: 15 U.S.C. 3719.
Dated: June 26, 2014.
Karen DeSalvo,
National Coordinator for Health Information Technology.
[FR Doc. 2014-16016 Filed 7-7-14; 8:45 am]
BILLING CODE 4150-45-P