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Board of Governors of the Federal Reserve
System, August 7, 2015.
Margaret McCloskey Shanks,
Deputy Secretary of the Board.
[FR Doc. 2015–19819 Filed 8–11–15; 8:45 am]
BILLING CODE 6210–01–P

access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT:

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–15–0650; Docket No. CDC–2015–
0064]

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:

The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on the Prevention Research
Centers Program National Evaluation
Reporting System. The information
collection system is designed to monitor
progress on a set of evaluation
indicators; demonstrate public health
impact and accountability to Congress,
CDC leadership, partner organizations,
and communities; increase PRC Program
visibility; generate knowledge and share
information within and outside the PRC
Program; and facilitate PRC Program
improvement.

SUMMARY:

Written comments must be
received on or before October 13, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0064 by any of the following methods:
Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road, NE.,
MS–D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For

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To

request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train

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personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Prevention Research Centers Program
National Evaluation Reporting System
(OMB No. 0920–0650, exp. 5/31/2016)—
Revision—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
In 1984, Congress passed Public Law
98–551 directing the Department of
Health and Human Services (DHHS) to
establish Centers for Research and
Development of Health Promotion and
Disease Prevention. In 1986, the CDC
received lead responsibility for this
program, referred to as the Prevention
Research Centers (PRC) Program. PRC
Program awardees are managed as a
CDC cooperative agreement with awards
made for five years.
In 2013, the CDC published program
announcement DP14–001 for the current
PRC Program funding cycle (September
30, 2014—September 29, 2019). Twentysix PRCs were selected through a
competitive, external, peer-review
process; the program is currently in its
first year of the five year funding cycle.
Each PRC is housed within an
accredited school of public health or an
accredited school of medicine or
osteopathy with a preventive medicine
residency program. The PRCs conduct
outcomes-oriented, applied prevention
research on a broad range of topics
using a multi-disciplinary and
community-engaged approach. Research
projects involve faculty from the funded
school and various departments within
the university, as well as community
partners. Partners include, but are not
limited to, state, local, and tribal health
departments, departments of education,
schools and school districts,
community-based organizations, health
providers, and other health
organizations. Partners collaborate with
the PRCs to assess community needs;
identify research priorities; set research
agendas; conduct research projects and
related activities such as training and
technical assistance; and disseminate
research results to public health
practitioners, researchers, and the
general public.
Each PRC receives funding from the
CDC to establish its core infrastructure
and functions and support a core
research project. Core research foci
reflect each PRC’s area of expertise and

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Federal Register / Vol. 80, No. 155 / Wednesday, August 12, 2015 / Notices
community needs. Most PRC core
research aligns with the health
disparities and goals outlined in
Healthy People 2020. In addition to core
research projects, most PRCs are
awarded funding to complete special
interest projects (SIPs) and conduct
other research projects.
The DP14–001 program
announcement included language that
was used to develop and operationalize
a set of 24 PRC Program evaluation
indicators. The PRC Program evaluation
indicators were collaboratively
developed in 2013 and 2014 with
internal and external stakeholders and
correspond to the PRC Program
conceptual framework (or logic model).
The PRC Program logic model identifies
program inputs, activities, outputs, and
outcomes. The list of indicators was
revised to better reflect program needs
and capture center and research
activities, outputs, and outcomes.
The CDC is currently approved to
collect information from the PRCs
through a structured telephone
interview and a web-based survey
hosted by a third-party. The web-based
survey is designed to collect
information on the PRCs’ collaborations
with health departments; formal
training programs and other training
activities; and other-funded research
projects conducted separate from their
core projects or SIP research. Structured
telephone interviews with key PRC
informants allow PRC Program staff to
collect indicator data that do not lend
themselves to a survey-based
methodology and require a qualitative
approach.
CDC requests OMB approval to revise
the information collection plan as
follows:
(1) The content of the web-based
survey will be updated to more closely
align with revised evaluation indicators
and/or to reflect the current needs of the

PRC Program. In addition, the webbased survey will be migrated from a
third party platform to a web-based data
collection system hosted on CDC
servers. Although the estimated burden
per response will increase, the revised
data collection system will be
comprehensive and will reduce the
need for follow-up clarification by PRC
Program awardees.
(2) CDC will continue to conduct
annual interviews (herein key informant
interviews) with PRC staff to capture
qualitative data about PRC activities and
outcomes; however, the content of the
in-depth interview will vary from year
to year. In the previous OMB approval
period, the annual interview focused on
implementation of environmental and
systems-wide strategies. CDC will
continue to collect this information on
a bi-annual basis (Key Informant
Interview Part I). In alternate years,
interview content will focus on PRC
partnerships (Key Informant Interview
Part II).
(3) CDC will bi-annually conduct
focus group discussions to capture
additional qualitative information about
network formation and cohesion. Biannually, PRC Program awardees will be
required to participate in focus group
discussions about PRC Network
formation and cohesion. In the same
years, PRC Program awardees will be
invited and encouraged, but not
required, to participate in focus group
discussions about Thematic Network
formation and cohesion.
CDC will continue to use the
information reported by PRCs to
identify training and technical
assistance needs, respond to requests for
information from Congress and other
sources, monitor grantees’ compliance
with cooperative agreement
requirements, evaluate progress made in
achieving goals and objectives, and

describe the impact and effectiveness of
the PRC Program.
The CDC currently funds 26 PRCs and
each center will annually report the
required information to the CDC. The
annualized estimated burden is
expected to increase. This increase
equates to an estimated weekly burden
of one hour per respondent and more
fully accounts for the burden of
preparing responses, as well as the
burden of reporting responses. Webbased data collection will occur on an
annual basis. The Key Informant
Interview (Part I) will be conducted in
years 2 and 4 of the current funding
cycle, and the Key Informant Interview
(Part II) will be conducted in year 3 of
the current funding cycle. During the
three-year OMB approval period, this
equates to two Part I interviews and one
Part II interview per PRC Program
awardee. Both focus group discussions
will take place in years 2 and 4 of the
current funding cycle. This equates to
one PRC Network focus group
discussion and one Thematic Network
focus group discussion per PRC Program
awardee during the three year OMB
approval period. Responses are
annualized in the burden table below.
The proposed web-based data
collection system will allow data entry
during the entire year, which will
enable respondents to distribute burden
throughout each funding year. Response
burden may decrease significantly in
years 2 through 5, since the web-based
data collection system will replicate a
number of data elements from year to
year, and respondents will only need to
enter changes.
OMB approval is requested for 3
years. CDC plans to implement revised
reporting requirements in December
2015. PRC Program awardees are
required to participate in information
collection. There are no costs to
respondents other than their time.

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent

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Prevention Research Center.

Total ...............

VerDate Sep<11>2014

Number of
responses per
respondent

Number of
respondents

Form name

Average burden
per response
(in hrs.)

Total burden
(in hrs.)

Web-based Data Collection .................

26

1

48

1,248

Key Informant Interview (Part I) ...........
Key Informant Interview (Part II) ..........
Focus Group Discussion: PRCs Network.
Focus Group Discussion: Thematic
Networks.

17
9
17

1
1
1

3
3
3

51
27
51

17

1

3

51

...............................................................

..............................

..............................

..............................

1,428

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Federal Register / Vol. 80, No. 155 / Wednesday, August 12, 2015 / Notices

Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2015–19799 Filed 8–11–15; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10143, CMS–
10572 and CMS–10564]

Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:

The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
any of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
DATES: Comments must be received by
October 13, 2015.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to http://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection

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document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number ll, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
http://www.cms.hhs.gov/
PaperworkReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
[email protected].
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10143 Monthly File of Medicaid/
Medicare Dual Eligible Enrollees
CMS–10572 Transparency in
Coverage Reporting by Qualified Health
Plan Issuers
CMS–10564 Home Health Face-toFace Encounter Clinical Templates
Under the PRA (44 U.S.C. 3501–
3520), federal agencies must obtain
approval from the Office of Management
and Budget (OMB) for each collection of
information they conduct or sponsor.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.

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Information Collection
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Monthly File of
Medicaid/Medicare Dual Eligible
Enrollees; Use: The monthly data file is
provided to CMS by states on dually
eligible Medicaid and Medicare
beneficiaries, listing the individuals on
the Medicaid eligibility file, their
Medicare status and other information
needed to establish subsidy level, such
as income and institutional status. The
file is used to count the exact number
of individuals who should be included
in the phased-down state contribution
calculation that month. CMS merges the
data with other data files and
establishes Part D enrollment for those
individuals on the file. The file may be
used by CMS partners to obtain accurate
counts of duals on a current basis. Form
Number: CMS–10143 (OMB Control
Number: 0938–0958); Frequency:
Monthly; Affected Public: State, Local,
or Tribal Governments; Number of
Respondents: 51; Total Annual
Responses: 612; Total Annual Hours:
6,120. (For policy questions regarding
this collection contact Vasanthi
Kandasamy at 410–786–0433).
2. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Transparency in
Coverage Reporting by Qualified Health
Plan Issuers; Use: Section 1311(e)(3) of
the Affordable Care Act requires issuers
of Qualified Health Plans (QHPs), to
make available and submit transparency
in coverage data. This data collection
would collect certain information from
QHP issuers in Federally-facilitated
Exchanges and State-based Exchanges
that rely on the federal IT platform (i.e.,
HealthCare.gov). HHS anticipates that
consumers may use this information to
inform plan selection.
Although this proposed data
collection is limited to certain QHP
issuers, HHS intends to phase in
implementation for other entities over
time. As stated in the final rule Patient
Protection and Affordable Care Act;
Establishment of Exchanges and
Qualified Health Plans; Exchange
Standards for Employers (77 FR 18310;
March 27, 2012), broader
implementation will continue to be
addressed in separate rulemaking issued
by HHS, and the Departments of Labor
and the Treasury (the Departments). For
State-based Exchanges not addressed in
the current proposal, standards will be
proposed later.
Consistent with Public Health Service
Act (PHS Act) section 2715A, which

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