60d FRN - published

Federal Register / Vol. 82, No. 80 / Thursday, April 27, 2017 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–17ADS; Docket No. CDC–2017–
0045]

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.
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 proposed information
collection project titled ‘‘Awardee Lead
Profile Assessment (ALPA).’’ The
information collection project includes
a questionnaire to collect information to
identify jurisdictional legal frameworks
governing funded childhood lead
poisoning prevention programs in the
United States, and strategies for
implementing childhood lead poisoning
prevention activities in the United
States.
DATES: Written comments must be
received on or before June 26, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0045 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.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
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: To
request more information on the

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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
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.

SUPPLEMENTARY INFORMATION:

AGENCY:

SUMMARY:

proposed project or to obtain a copy of
the information collection plan and
instruments, contact Leroy A.
Richardson, of Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., MS–D74, Atlanta, Georgia
30329; phone: 404–639–7570; Email:
omb@cdc.gov.

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Proposed Project
Awardee Lead Profile Assessment
(ALPA)—NEW—National Center for
Environmental Health (NCEH), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) is requesting a threeyear clearance for a new information
collection project titled ‘‘Awardee Lead
Profile Assessment (ALPA).’’ The goal of
this project is to build on an existing
childhood lead poisoning prevention
program. CDC will obtain program
management information from
participating state and local
governments that are awardees under
the CDC Healthy Homes and Lead
Poisoning Prevention Program
(HHLPPP) FY17 Funding Opportunity
Announcement (FOA No. CDC–RFA–
EH17–1701PPHF17). This annual
information collection will be used: (1)
To identify common characteristics of
funded childhood lead poisoning
prevention programs; and (2) inform
guidance and resource development in
support of the ultimate program goal,
which is blood lead elimination in
children.
The dissemination of these ALPA
results will ensure that both funded and
non-funded jurisdictions are able to: (1)
Identify policies and other factors that
support or hinder childhood lead
poisoning prevention efforts; (2)
understand what strategies are being
used by funded public health agencies
to implement childhood lead poisoning
prevention activities; and (3) use this
knowledge to develop and apply similar
strategies to support the national agenda
to eliminate childhood lead poisoning.
This program management
information will be collected annually
from 45 awardees, using two data
collection modes. We anticipate that the
majority, 40 respondents, will choose
the Web survey due to the ease of use,
and that 5 respondents will choose the
MSWord format mode.
We estimate the time burden to be the
same, 7 minutes per response,
regardless of data collection mode (Web
survey or Word format). This estimate is
based on a 2015 survey among 35
former awardees titled ‘‘Baseline Profile
of State and Local Healthy Homes and
Lead Poisoning Prevention Programs
(PROF–LEAD),’’ approved under the
generic clearance for ‘‘Information
Collections to Advance State, Tribal,
Local, and Territorial (STLT)
Governmental Health’’ (OMB Control
No. 0920–0879; expiration date 03/31/
2018). Due to its success, the PROF–

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Federal Register / Vol. 82, No. 80 / Thursday, April 27, 2017 / Notices

LEAD questionnaire is now proposed as
an annual reporting requirement for

awardees under the FY17 FOA, as the
ALPA questionnaire.

There is no cost to the respondents
other than their time. The total annual
time burden requested is six hours.

ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)

Total
burden
hours

Form name

State And Local Governments (or
their bona fide fiscal agents).

Awardee Lead Profile Assessment
(ALPA) Questionnaire—Web survey.
ALPA Questionnaire—Word format

40

1

7/60

5

5

1

7/60

1

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

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

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

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

6

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

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. 2017–08539 Filed 4–26–17; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–17–1074]

Agency Forms Undergoing Paperwork
Reduction Act Review

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Number of
responses per
respondent

Number of
respondents

Type of respondent

The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (b) Evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected; (d) Minimize the burden of
the collection of information on those
who are to respond, including through
the use of appropriate automated,
electronic, mechanical, or other

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technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and (e) Assess information
collection costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Written
comments and/or suggestions regarding
the items contained in this notice
should be directed to the Attention:
CDC Desk Officer, Office of Management
and Budget, Washington, DC 20503 or
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Colorectal Cancer Control Program
(CRCCP) Monitoring Activities (OMB
Control Number 0920–1074, expires 06/
30/2019)—Revision—National Center
for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
CDC is requesting a revision to the
approved information collection under
OMB Control Number 0920–1074. CDC
proposes use of a revised grantee survey
instrument, as well as a revised cliniclevel data collection template. The
number of respondents will also
decrease from 31 to 30 grantees, and the
total estimated annualized burden will
decrease.
Colorectal cancer (CRC) is the second
leading cause of death from cancer in
the United States among cancers that
affect both men and women. CRC
screening has been shown to reduce
incidence of and death from the disease.
Screening for CRC can detect disease
early when treatment is more effective
and prevent cancer by finding and
removing precancerous polyps. Of
individuals diagnosed with early stage

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CRC, more than 90% live five or more
years. To reduce CRC morbidity,
mortality, and associated costs, use of
CRC screening tests must be increased
among age-eligible adults with the
lowest CRC screening rates.
The purpose of the Colorectal Cancer
Control Program (CRCCP): Organized
Approaches to Increase Colorectal
Cancer Screening (CDC–RFA–DP15–
1502), is to increase CRC screening rates
among an applicant defined target
population of persons 50–75 years of
age within a partner health system
serving a defined geographical area or
disparate population. The CRCCP
includes 30 grantees that are state
governments or bona-fide agents,
universities, and tribal organizations.
The CRCCP was significantly
redesigned in 2015 and has two
components. Under Component 1, all
grantees receive funding to support
partnerships with health systems to
implement up to four priority evidencebased interventions (EBIs) described in
the Guide to Community Preventive
Services, as well as other supporting
activities (SAs). Grantees must
implement at least two EBIs in each
partnering health system. Under
Component 2, six of the 30 grantees
provide direct screening and follow-up
clinical services for a limited number of
individuals aged 50–64 in the program’s
priority population who are
asymptomatic, at average risk for CRC,
have inadequate or no health insurance
for CRC screening, and are low income.
Two forms of data collection have
been implemented to assess program
processes and outcomes. In Program
Year 1, the annual grantee survey
monitored grantee program
implementation, including (1) program
management, (2) implementation of the
EBIs and SAs, (3) health information
technology (IT), (4) partnerships, (5)
data use, (6) training and technical
assistance (TA), and (7) clinical service
delivery (for programs receiving

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