30d FRN - published Round 1_5/19

Federal Register / Vol. 88, No. 97 / Friday, May 19, 2023 / Notices
1. Lake Central Financial, Inc.,
Annandale, Minnesota; to acquire State
Bank of Danvers, Benson, Minnesota.
B. Federal Reserve Bank of Kansas
City (Jeffrey Imgarten, Assistant Vice
President) One Memorial Drive, Kansas
City, Missouri 64198–0001. Comments
can also be sent electronically to
[email protected].
1. Vista Holding Company, St. Louis,
Missouri; to become a bank holding
company by acquiring Mohler
Bancshares, Inc., and thereby indirectly
acquiring The First National Bank of
Harveyville, both of Harveyville,
Kansas.
C. Federal Reserve Bank of San
Francisco: (Joseph Cuenco, Assistant
Vice President) 101 Market Street, San
Francisco, California 94105–1579.
Comments can also be sent
electronically to:
sf.fisc.comments.applications@
sf.frb.org.
1. BancPacific Financial Holding
Corporation, Hagatna, Guam, and
Marianas Finance Corporation,
Tamuning, Guam; to become bank
holding companies by acquiring
BancPacific Ltd., Hagatna, Guam, upon
the conversion of BankPacific Ltd., from
a savings association to a commercial
bank.
Board of Governors of the Federal Reserve
System.
Michele Taylor Fennell,
Deputy Associate Secretary of the Board.
[FR Doc. 2023–10761 Filed 5–18–23; 8:45 am]
BILLING CODE P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–23–23CO]

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Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘National
Center for Health Statistics (NCHS)
Rapid Surveys System (RSS)’’ to the
Office of Management and Budget
(OMB) for review and approval. CDC
previously published a ‘‘Proposed Data
Collection Submitted for Public
Comment and Recommendations’’
notice on February 17, 2023 to obtain
comments from the public and affected
agencies. CDC received two comments
related to the previous notice. This
notice serves to allow an additional 30

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days for public and affected agency
comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(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.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
National Center for Health Statistics
(NCHS) Rapid Surveys System (RSS)—
New—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 (HHS),
acting through NCHS, collect data about
the health of the population of the
United States. The NCHS Rapid Surveys

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System (RSS) will collect data on
emerging public health topics, attitudes,
and behaviors using cross-sectional
samples from two commercially
available, national probability-based
online panels. The RSS will then
combine these data to form estimates
that approximate national
representation in ways that many data
collection approaches cannot. The RSS
is intended to collect data in contexts in
which decision makers’ need for timesensitive data of known quality about
emerging and priority health concerns is
a higher priority than their need for
statistically unbiased estimates.
The RSS will complement NCHS’s
current household survey systems. As
quicker turnaround surveys that require
less accuracy and precision than CDC’s
more rigorous population representative
surveys, the RSS will incorporate
multiple mechanisms to carefully
evaluate the resulting survey data for
their appropriateness for use in public
health surveillance and research (e.g.,
hypothesis generating) and facilitate
continuous quality improvement by
supplementing these panels with
intensive efforts to understand how well
the estimates reflect populations at most
risk. The RSS data dissemination
strategy will communicate the strengths
and limitations of data collected
through online probability panels as
compared to more robust data collection
methods.
The RSS has three major goals: (1) to
provide CDC and other partners with
time-sensitive data of known quality
about emerging and priority health
concerns; (2) to use these data
collections to continue NCHS’s
evaluation of the quality of public
health estimates generated from
commercial online panels; and (3) to
improve methods to communicate the
appropriateness of public health
estimates generated from commercial
online panels.
Each round’s questionnaire will
consist of four main components: (1)
basic demographic information on
respondents to be used as covariates in
analyses; (2) new, emerging, or
supplemental content proposed by
NCHS, other CDC Centers, Institute, and
Offices, and other HHS agencies; (3)
questions used for calibrating the survey
weights; and (4) additional content
selected by NCHS to evaluate against
relevant benchmarks. NCHS will use
questions from Components 1 and 2 to
provide relevant, timely data on new,
emerging, and priority health topics to
be used for decision making. NCHS will
use questions from Components 3 and 4
to weight and evaluate the quality of the
estimates coming from questions in

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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.

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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:

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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

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