60-day Federal Register Notice

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Federal Register / Vol. 81, No. 143 / Tuesday, July 26, 2016 / Notices

infrastructure to implement and sustain
science-based, culturally appropriate
High Impact HIV Prevention (HIP)
interventions and public health
strategies.
Applicants selected for funding must
work with the CDC-funded CBA
providers to develop and implement a
Capacity Building Assistance Strategic
Plan (CBASP). The information
collected via this process will be used
to construct a CBASP for each funded
organization in collaboration with
CDC’s Capacity Building Branch (CBB).
CBA Providers will provide technical
assistance and training to ensure that
the CBOs and Partnerships have the
skills and support they need to
successfully implement their CDCfunded HIV High Impact Prevention
program.

CBA providers will utilize the CBO
CBA Assessent Tool which offers a
mixed-method data collection approach
with close-ended, and open-ended
questions. CBOs will complete and
submit the completed web-based Tool,
which will be discussed, and needs
confirmed, during a follow-up phone
contact assessment. A follow-up site
visit may be recommended for CBOs
with dire needs (up to 20%), which will
be scheduled upon approval by the
Project Officer and Program Consultant.
Data from all completed Tools will be
analyzed and used to develop a CBA
Strategic Plan (CBASP) which will be
housed in the Capacity Assistance
Request Information System (managed
by the Capacity Building Branch), in the
Division of HIV/AIDS Prevention and
consulted by CBA Providers assigned to

respond to the prioritized CBOs’ CBA
needs.
By the end of the project, the
participating CBOs and Partnerships
will have tailored CBA strategic plans
that they can use to help sustain their
programs across and beyond the life of
their funding. Based on these plans, the
CBA providers in collaboration with
CDC will be able to better identify and
address those needs most reported by
CBOs. Finally, the Capacity Building
Branch will be able to refine its
approach to conceptualizing and
providing CBA on a national level in the
most cost-effective manner possible.
There is no cost to respondents other
than their time. The total annual burden
hours are 240.

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents

Form name

Number of
respondents

Number of
responses per
respondent

Avg. burden
per response
(in hrs.)

CBO Grantees ................................................

CBO CBA Assessment Tool ..........................

120

1

2

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. 2016–17643 Filed 7–25–16; 8:45 am]
BILLING CODE 4163–18–P

Centers for Disease Control and
Prevention
[60 Day–16–0214; Docket No. CDC–2016–
0069]

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 effort 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 National Health

srobinson on DSK5SPTVN1PROD with NOTICES

SUMMARY:

20:28 Jul 25, 2016

You may submit comments,
identified by Docket No. CDC–2016–
0069 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.

ADDRESSES:

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

VerDate Sep<11>2014

Interview Survey (NHIS). The annual
National Health Interview Survey is a
major source of general statistics on the
health of the U.S. population.
DATES: Written comments must be
received on or before September 26,
2016.

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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.

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

FOR FURTHER INFORMATION CONTACT:

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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

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Federal Register / Vol. 81, No. 143 / Tuesday, July 26, 2016 / Notices
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.
Proposed Project
National Health Interview Survey
(NHIS) (OMB No. 0920–0214, expires
12/31/2017)—Revision—National
Center for Health Statistics (NCHS),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C.), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on the extent and nature of
illness and disability of the population
of the United States.
The annual National Health Interview
Survey is a major source of general
statistics on the health of the U.S.

mental health. Questions from 2016 on
balance and Hepatitis B and C screening
have been removed. In addition to these
core and supplemental modules, a
subsample of NHIS respondents and/or
members of commercial survey panels
may be identified to participate in short,
web-based methodological and
cognitive testing activities that will
inform the upcoming 2018 NHIS
questionnaire redesign. The aims of
these standalone assessments include
pilot testing new and/or updated
questionnaire items, evaluating the
impact of different categorical response
option formats on answer choices, and
measuring respondent comprehension
of health care-related terms and
concepts.
In accordance with the 1995 initiative
to increase the integration of surveys
within the DHHS, respondents to the
NHIS serve as the sampling frame for
the Medical Expenditure Panel Survey
conducted by the Agency for Healthcare
Research and Quality. The NHIS has
long been used by government,
academic, and private researchers to
evaluate both general health and
specific issues, such as smoking,
diabetes, health care coverage, and
access to health care. It is a leading
source of data for the Congressionallymandated ‘‘Health US’’ and related
publications, as well as the single most
important source of statistics to track
progress toward the National Health
Promotion and Disease Prevention
Objectives, ‘‘Healthy People 2020.’’
There is no cost to the respondents
other than their time. The estimated
annualized burden hours for this data
collection are 502 hours.

population and has been in the field
continuously since 1957. Clearance is
sought for three years, to collect data for
2017–2019.
This voluntary and confidential
household-based survey collects
demographic and health-related
information from a nationallyrepresentative sample of
noninstitutionalized, civilian persons
and households throughout the country.
Personal identification information is
requested from survey respondents to
facilitate linkage of survey data with
health-related administrative and other
records. In 2017 the NHIS will collect
information from approximately 45,000
households, which contain about
100,000 individuals. Information is
collected using computer assisted
personal interviews (CAPI).
A core set of data is collected each
year that remains largely unchanged,
whereas sponsored supplements vary
from year to year. The core set includes
socio-demographic characteristics,
health status, health care services, and
health behaviors. For 2017,
supplemental questions will be cycled
in pertaining to alternative and
integrative medicine, cognitive
disability, and receipt of culturally and
linguistically appropriate health care
services, epilepsy, and heart disease and
stroke. Supplemental topics that
continue or are enhanced from 2016
pertain to the Affordable Care Act,
chronic pain, Crohn’s disease and
colitis, diabetes, disability and
functioning, family food security, ABCS
of heart disease and stroke prevention,
immunizations, smokeless tobacco and
e-cigarettes, vision, and children’s

srobinson on DSK5SPTVN1PROD with NOTICES

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Number of
responses per
respondent

Average
burden per
response
(in hours)

Total
burden
(in hours)

Type of Respondent

Form name

Adult Family Member ........................
Sample Adult .....................................
Adult Family Member ........................
Adult Family Member ........................
Adult Family Member ........................
Adult Family Member ........................

Family Core ......................................
Adult Core ........................................
Child Core ........................................
Supplements ....................................
Methodological Projects ...................
Re-interview Survey .........................

45,000
36,000
14,000
45,000
15,000
5,000

1
1
1
1
1
1

23/60
15/60
10/60
15/60
30/60
5/60

17,250
9,000
2,333
15,000
5,000
417

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

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

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

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

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

49,000

VerDate Sep<11>2014

20:28 Jul 25, 2016

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Federal Register / Vol. 81, No. 143 / Tuesday, July 26, 2016 / 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. 2016–17611 Filed 7–25–16; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30 Day–16–15AUK]

Agency Forms Undergoing Paperwork
Reduction Act Review
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 agencies 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
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 [email protected]. 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
Monitoring and Reporting System for
the Prescription Drug Overdose
Prevention for States Cooperative
agreement—New—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Drug overdose is the leading cause of
injury death in the United States.
Opioid-prescribing behaviors are
associated with an increased risk for
morbidity and mortality. While opioid
pain relievers can play an important
role in the management of some types
of pain, the overprescribing of these
powerful drugs has fueled a national
epidemic of prescription drug abuse and
overdose. To reverse this complex
epidemic and prevent future overdose,
abuse, and misuse, the Centers for
Disease Control and Prevention (CDC)
provides support to states to improve

surveillance. Support and guidance for
these programs have been provided
through cooperative agreement funding
and technical assistance administered
by CDC’s National Center for Injury
Prevention and Control (NCIPC).
The Centers for Disease Control and
Prevention (CDC) seeks new OMB
approval to collect information from
awardees funded under the Prescription
Drug Overdose Prevention for States
(CDC–RFA–CE15–1501) cooperative
agreement, for program monitoring and
improvement among funded state health
departments. Awardees will report
progress and activity information to
CDC on an annual schedule using an
Excel-based fillable electronic
templates, pre-populated to the extent
possible by CDC staff. In Year 1, each
awardee will have additional burden
related to initial collection of the
reporting tools. After completing the
initial population of the tools, pertinent
information only needs to be updated
for each annual report. The same
instruments will be used for all
information collection and reporting.
CDC will use the information
collected to monitor each awardee’s
progress and to identify facilitators and
challenges to program implementation
and achievement of outcomes.
Monitoring allows CDC to determine
whether an awardee is meeting
performance and budget goals and to
make adjustments in the type and level
of technical assistance provided to
them, as needed, to support attainment
of their performance measures.
The total estimated annualized
burden for this collection is 812 hours.
OMB approval is requested for three
years. Participation in the information
collection is required as a condition of
funding. There are no costs to
respondents other than their time.

srobinson on DSK5SPTVN1PROD with NOTICES

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Type of respondents

Form name

State and Territorial Health Department Program Awardees.

Initial
population—Annual
reporting—
Progress Report Tool.
Annual reporting—Progress Report Tool .......
Annual reporting—Plan Tool ..........................

1

20

29
29

1
1

4
4

[FR Doc. 2016–17604 Filed 7–25–16; 8:45 am]
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Average
burden per
response
(in hours)

29

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.

VerDate Sep<11>2014

Number of
responses per
respondent

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