60d FRN published

60d FRN - published.pdf

The Childcare Survey of Activity and Wellness (C-SAW) Pilot Study

60d FRN published

OMB: 0920-1277

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Federal Register / Vol. 85, No. 211 / Friday, October 30, 2020 / Notices
online and all active EAS/Comprizon
contracts were migrated into the new
EASi application. A complete snapshot
of the EAS/Comprizon data was taken
and stored in the Business Intelligence
(BI) database. The snapshot still exists
in the BI database today and is used for
querying and reporting purposes. None
of the EAS/Comprizon records currently
in the BI database contain PII. The
replacement system for EAS, EASi, also
does not contain PII. The vendor
information is directly collected and
stored in SAM.
SYSTEM NAME AND NUMBER:

GSA/PBS–6 Electronic Acquisition
System (EAS).
HISTORY:

73 FR 22389.
Richard Speidel,
Chief Privacy Officer, Office of the Deputy
Chief Information Officer, General Services
Administration.
[FR Doc. 2020–24077 Filed 10–29–20; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–21–1277; Docket No. CDC–2020–
0109]

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 and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on the
existing information collection project
titled The Childcare Survey of Activity
and Wellness (C–SAW) Pilot Study. The
pilot study will determine the current
practices and policies of early care and
education (ECE) providers in four states
around nutrition, physical activity, and
wellness and will inform the
development of a potential national
surveillance system.

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SUMMARY:

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CDC must receive written
comments on or before December 29,
2020.

DATES:

You may submit comments,
identified by Docket No. CDC–2020–
0109 by any of the following methods:
• Federal eRulemaking Portal:
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–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
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
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–
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 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;
ADDRESSES:

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3. Enhance the quality, utility, and
clarity of the information to be
collected; and
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.
5. Assess information collection costs.
Proposed Project
The Childcare Survey of Activity and
Wellness (C–SAW) Pilot Study—
Revision—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) works to promote
optimal nutrition, physical activity, and
wellness in early care and education
(ECE) facilities for children 0–5 years of
age. Consistent with this mission, and
with clear evidence that ECE facilities
can impact the habits and preferences of
young children, CDC obtained OMB
approval (OMB Control No. 0920–1277,
Expiration Date 12/31/2020) to conduct
a pilot survey to better understand ECE
center practices related to nutrition,
physical activity, and wellness. CDC
was unable to collect the information as
planned due to closures of ECE centers
because of the COVID–19 pandemic.
CDC is requesting an extension of the
collection for two years due to the
COVID–19 pandemic and its impact on
information collection and to collect 10
additional COVID–19 related questions
on the survey to understand the impact
of COVID–19 on our topic areas of child
care center status, nutrition, physical
activity and wellness The additional
questions are expected to minimally
affect burden. These critical data are
used to effectively inform state and
national programs.
Data collected from this pilot survey
will be used to understand the current
practices of ECE centers in a
representative sample in four states.
This initial C–SAW will establish
baseline measures of the prevalence of
specific practices related to nutrition,
physical activity, and wellness in a
standard way across states. This
baseline will also allow CDC and state
partners to better understand ECE center
needs and provide opportunities for
collaboration and areas for improvement
at the state and national levels. Second,
the survey will be used to inform the
development of a potential national

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Federal Register / Vol. 85, No. 211 / Friday, October 30, 2020 / Notices

surveillance system enabling states and
CDC to track changes over time and
obtain data to guide the planning,
implementation, and evaluation of
national and state obesity prevention
efforts.
A sample of approximately 1,200 ECE
centers across four states will be
recruited to participate in this one-time
data collection effort. Each center will
receive a recruitment letter introducing

the survey, explaining its objectives and
the importance of their participation,
and instructions for completing the
survey. It is anticipated that most
responses will be submitted online via
the internet. However, paper surveys
will be available upon request.
Approximately two weeks after the
initial recruitment letter is mailed, all
sampled centers will receive a reminder
postcard. Approximately four weeks

after the initial recruitment letter is
mailed, non-respondents will be sent
another letter along with a hardcopy of
the questionnaire.
Participation in this study is
completely voluntary and there are no
costs to the respondent other than their
time. The estimated annualized burden
hours is 409. The approval request is for
two years.

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Average
burden per
response
(in hours)

Total burden
(in hours)

Form name

ECE Director or Administrator ..........
ECE Director or Administrator ..........

Recruitment Letter ............................
Web/Mail Survey ..............................

1,140
627

1
1

5/60
30/60

95
314

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

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

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

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

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

409

Jeffrey M. Zirger,
Lead, 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. 2020–24230 Filed 10–28–20; 4:15 pm]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention

National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention, Department of Health
and Human Services.
ACTION: Notice.
AGENCY:

NIOSH gives notice of a
decision to evaluate a petition to
designate a class of employees from the
Pinellas Plant in Clearwater, Florida, to
be included in the Special Exposure
Cohort under the Energy Employees
Occupational Illness Compensation
Program Act of 2000.
FOR FURTHER INFORMATION CONTACT:
Grady Calhoun, Director, Division of
Compensation Analysis and Support,
National Institute for Occupational
Safety and Health, 1090 Tusculum
Avenue, MS C–46, Cincinnati, OH
45226–1938, Telephone 513–533–6800.
Information requests can also be
submitted by email to [email protected].
SUMMARY:

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Pursuant
to 42 CFR 83.12, the initial proposed
definition for the class being evaluated,
subject to revision as warranted by the
evaluation, is as follows:
Facility: Pinellas Plant.
Location: Clearwater, Florida.
Job Titles and/or Job Duties: All
employees who worked in any areas of
Pinellas Plant.
Period of Employment: May 19, 1957
through December 31, 1997.

SUPPLEMENTARY INFORMATION:

Authority: 42 CFR 83.9–83.12.

Decision To Evaluate a Petition To
Designate a Class of Employees From
the Pinellas Plant in Clearwater,
Florida, To Be Included in the Special
Exposure Cohort

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Number of
respondents

Type of respondents

John J. Howard,
Director, National Institute for Occupational
Safety and Health.
[FR Doc. 2020–24123 Filed 10–29–20; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–381]

Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
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

SUMMARY:

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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
the necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions,
the accuracy of the estimated burden,
ways to enhance the quality, utility, and
clarity of the information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
December 29, 2020.
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
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 llll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.

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