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: VerDate Mar<15>2010 20:08 Jul 08, 2014 Jkt 232001 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 PO 00000 Frm 00046 Fmt 4703 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 09JYN1 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 VerDate Mar<15>2010 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 VerDate Mar<15>2010 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
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