60d FRN - published

32220

Federal Register / Vol. 88, No. 97 / Friday, May 19, 2023 / Notices

Components 1 and 2. Components 1 and
2 will contain different topics in each
round of the survey. NCHS will submit
a 30-day Federal Register Notice with
information on the contents of each
round of data collection.
In the first round of RSS, contributed
content is included on knowledge,
attitudes, and beliefs regarding Long
COVID; mammograms and notifications
about breast density; medical
procedures on fallopian tubes and
ovaries; concerns about genetic testing;
knowledge about the relationship
between alcohol use and cancer;
sunscreen use and beliefs about
sunscreen; use of chemical hair
straighteners, relaxers, or pressing
products; use of air cleaners or purifiers
in the home; intimate partner violence;
and new questions about race and
ethnicity to assist in the development of
recommendations on how to improve
the quality and usefulness of OMB
Statistical Policy Directive No. 15.
NCHS will calibrate data from the
RSS to other surveys. Questions used for
calibration in the first round of RSS will
include marital status and employment,
social and work limitations, use of the
internet in general and for medical
reasons, telephone use, civic

engagement, and language used at home
and in other settings. All these
questions have been on the National
Health Interview Survey (NHIS) in prior
years allowing calibration to these data.
Finally, several questions that were
previously on NHIS will be used for
benchmarking. Panelists in the RSS will
be asked if they have been told they
have chronic conditions including
hypertension, high cholesterol, coronary
heart disease, asthma, diabetes, and
Long COVID. Questions about selfreported health; pregnancy status;
height and weight, difficulty paying
medical bills; access to and use of
medical, dental, eye care and physical
therapy; preventive care; mental health;
and cigarette use will be used to
benchmark the RSS to NCHS surveys.
The RSS is designed to have four
rounds of data collection each year with
data being collected by two contractors
with probability panels. A crosssectional nationally representative
sample will be drawn from the online
probability panel maintained by each of
the contractors. As part of the base
(minimum sample size), each round of
data collection will collect 2,000
responses per quarter. The RSS can be
expanded by increasing the number of

completed responses per round or the
number of rounds per year as needed up
to a maximum of 28,000 responses per
year per contractor or 56,000 total
responses per year. Additionally, each
data collection may include up to 2,000
additional responses per quarter (8,000
for the year) to improve
representativeness. This increases the
maximum burden by up to 16,000
responses per year. The RSS may also
target individual surveys to collect data
only from specific subgroups within
existing survey panels and may
supplement data collection for such
groups with additional respondents
from other probability or nonprobability
samples. An additional 12,000
responses per year may be used for
these developmental activities. Survey
questions being asked of the panelists
will be cognitively tested. This cognitive
testing will help survey users interpret
the findings by understanding how
respondents answer each question.
CDC requests OMB approval for an
estimated 28,079 burden hours annually
over the course of the three-year
approval period. There are no costs to
respondents other than their time.

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents

Adults
Adults
Adults
Adults
Adults

18+
18+
18+
18+
18+

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

Number of
respondents

Form name

Base Surveys .........................................................................
Potential Sample Expansion ..................................................
Additional Surveys to Increase Representativeness .............
Developmental: Additional Surveys for Specific Subgroups ..
Cognitive interviews ...............................................................

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
[FR Doc. 2023–10745 Filed 5–18–23; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–23–0841; Docket No. CDC–2023–
0038]

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.

ddrumheller on DSK120RN23PROD with NOTICES1

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

SUMMARY:

VerDate Sep<11>2014

18:30 May 18, 2023

Jkt 259001

PO 00000

Frm 00045

Fmt 4703

Sfmt 4703

Number of
responses per
respondent

16,000
40,000
16,000
12,000
80

1
1
1
1
1

Average
burden per
response
(in hours)
20/60
20/60
20/60
20/60
1

agencies the opportunity to comment on
a continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled ‘‘Management
Information System for Comprehensive
Cancer Control Programs’’. The CDC
will use annual key informant
interviews and biennial NCCCP survey
to monitor program outcomes and report
progress to CDC yearly.
DATES: CDC must receive written
comments on or before July 18, 2023.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2023–
0038 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600

E:\FR\FM\19MYN1.SGM

19MYN1

32221

Federal Register / Vol. 88, No. 97 / Friday, May 19, 2023 / Notices
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to
the address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 404–639–7570; Email: omb@
cdc.gov.
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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;

Agents, to design, implement, and
evaluate comprehensive cancer control
plans to reduce the burden of cancer
locally. Support for these programs is a
cornerstone of CDC efforts to reduce the
burden of cancer throughout the nation.
Awards to individual applicants are
made for a five-year program period.
Continuation awards for subsequent
budget periods are made on the basis of
satisfactory progress in achieving both
national and program-specific goals and
objectives, as well as the availability of
funds.
In 2022, 66 recipients were selected
for funding for DP22–2202 (‘‘Cancer
Prevention and Control Programs for
State, Territorial, and Tribal
Organizations’’) to implement a program
to support cancer coalition efforts that
leverage resources to plan and
implement evidence-based strategies to
promote the primary prevention of
cancer; support cancer early detection
efforts; address the needs of cancer
survivors; and promote health equity.
Consistent with programmatic
changes, the proposed data collection
plan for DP22–2202 has been redesigned
to increase efficiency by updating
existing and adding new data collection
instruments. This revised data
collection will allow CDC to continue
providing routine feedback to recipients
based on their data submissions, tailor
technical assistance as needed, support
program planning, and assess program
outcomes. In this Revision request, CDC
seeks OMB approval to use an interview
and web-based survey to collect, store,
retrieve, share, and report accurate and
timely information to monitor and
evaluate recipient performance.
OMB approval is requested for three
years. The total estimated annualized
burden hours requested are 401 hours.
Participation is voluntary and there are
no costs to respondents other than their
time.

2. 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;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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 submissions
of responses; and
5. Assess information collection costs.
Proposed Project
Management Information System for
Comprehensive Cancer Control
Programs (OMB Control No. 0920–0841,
Exp. 7/31/2023)—Revision—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC)
Background and Brief Description
CDC requests a Revision of the
National Comprehensive Cancer Control
Program’s (NCCCP) Management
Information System for Comprehensive
Cancer Control Programs (OMB Control
No. 0920–0841, Exp. 7/31/2023) to
continue electronic data collection of
information about the NCCCP, funded
by the Comprehensive Cancer Control
Branch of the CDC.
The Comprehensive Cancer Control
Branch manages the NCCCP, which
provides funding to 66 State health
departments and the District of
Columbia, US Territories and Freely
Associated States, Federally Recognized
American Indian Tribes, Tribal
Organizations, Alaska Native
Organizations, and Urban Indian
Organizations; or their Bona Fide

ddrumheller on DSK120RN23PROD with NOTICES1

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Average
burden per
response
(in hours)

Number of
responses per
respondent

Total burden
(in hours)

Type of respondents

Form name

Program Director for State-, Tribal-,
or Territorial-based Cancer Prevention and Control Program.
Program Director for State-, Tribal-,
or Territorial-based Cancer Prevention and Control Program.

NCCCP Survey ................................

132

2

45/60

198

NCCCP Annual Key Informant Interview.

54

5

90/120

203

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

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

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

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

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

401

VerDate Sep<11>2014

18:30 May 18, 2023

Jkt 259001

PO 00000

Frm 00046

Fmt 4703

Sfmt 4703

E:\FR\FM\19MYN1.SGM

19MYN1

32222

Federal Register / Vol. 88, No. 97 / Friday, May 19, 2023 / Notices

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
[FR Doc. 2023–10747 Filed 5–18–23; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–23–23EZ; Docket No. CDC–2023–
0037]

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 the opportunity to comment on
a proposed information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Workplans for
Regional Centers to Enhance Public
Health Preparedness and Response. This
data collection is designed to support
regional centers’ creation of a five-year
workplan which addresses focus areas
that would benefit from use of new or
enhanced evidence-based strategies
(EBSI), existing and needed approaches
to meet regional emergency
preparedness and EBSI needs, proposed
measures to ensure strategies and
interventions are effectively
implemented, and regional
sustainability of evidence-based practice
beyond the five-year workplan.
DATES: CDC must receive written
comments on or before July 18, 2023.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2023–
0037 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without

ddrumheller on DSK120RN23PROD with NOTICES1

SUMMARY:

VerDate Sep<11>2014

18:30 May 18, 2023

Jkt 259001

change, all relevant comments to
www.regulations.gov. Please note:
Submit all comments through the
Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to
the address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 404–639–7570; Email: omb@
cdc.gov.
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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. 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;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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 submissions
of responses; and
5. Assess information collection costs.
Proposed Project
Workplans for Regional Centers to
Enhance Public Health Preparedness
and Response—New—Office of
Readiness and Response (ORR), Centers

PO 00000

Frm 00047

Fmt 4703

Sfmt 4703

for Disease Control and Prevention
(CDC).
Background and Brief Description
Since 2001, CDC has supported the
development, implementation,
evaluation, translation and
dissemination of research findings,
strategies, and interventions to improve
public health preparedness and
response systems, infrastructures,
processes, and practices. This includes
the long-standing PHEP cooperative
agreement, CDC’s Public Health Crisis
Response Funding, and support for
applied research and evaluation,
metrics, measures, tools, and training
development.
In 2021, with contract support, CDC’s
Office of Applied Research (OAR)
initiated 12 scoping reviews, six
landscape analyses, and one systematic
review to conduct deeper dives into
topics such as trust in public health
preparedness and response, emergency
communications strategies with people
with limited English proficiency, public
health emergency preparedness and
response (PHEPR) practice in rural and
tribal communities, and use of health
equity coordinators in incident
management. The results of these
reviews show great breadth in the
PHEPR field as it relates to knowledge
available to support current practice and
highlights the need to expand
knowledge to address specific gaps.
These needs and gaps may differ across
geographical regions and within those
regions at the state or local level. To
address needs to increase the uptake of
evidence-based interventions, in
December 2022, through Section 2231 of
the Federal appropriations for fiscal
year 2023, CDC was directed to support
not fewer than 10 Centers for PHEPR
that are equally distributed among the
geographical regions of the U.S.
(referred to as the ‘‘network of centers’’.
The goal of this project is to conduct
a needs assessment to enhance the
PHEPR capabilities in the 10 designated
Health and Human Services (HHS)
regions by creating an optimal five-year
workplan to implement evidence-based
strategies or interventions (EBSI) in this
space. The five-year workplan will
address: (1) focus areas that would
benefit from use of new or enhanced
evidence-based strategies or
interventions (EBSI) or interventions,
particularly to increase health equity;
(2) existing and needed approaches as
well as STLT health departments’
capacity and capability to meet regional
emergency preparedness and EBSI
needs; (3) prioritized strategies and
interventions to implement (and
develop, if needed) EBSIs over the next

E:\FR\FM\19MYN1.SGM

19MYN1