Proposed Data Collection Submitted for Public Comment and Recommendations, 43254-43255 [2021-16825]
Download as PDF
<![CDATA[
43254
Federal Register / Vol. 86, No. 149 / Friday, August 6, 2021 / Notices
information and will not ask questions
of a sensitive nature, such as sexual
behavior and attitudes, religious beliefs,
and other matters that are commonly
considered private. The total estimated
burden hours requested are 13,075.
There is no cost to respondents other
than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Annual
frequency
per response
Hours
per response
Type of collections
Individuals and Households, Businesses and Organizations,
State, Local or Tribal Government.
Print Surveys .........................
50,000
1
15/60
Focus Groups ........................
Online Surveys ......................
100
1500
1
1
2
15/60
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–16822 Filed 8–5–21; 8:45 am]
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
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
Understanding important issues in
ovarian cancer survivorship (OCS)
project. The OCS project aims to better
understand the needs of ovarian cancer
survivors and how to more effectively
develop interventions targeted to this
population.
DATES: CDC must receive written
comments on or before October 5, 2021.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2021–
0077 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
VerDate Sep<11>2014
19:29 Aug 05, 2021
Jkt 253001
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:
404–639–7118; 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,
FOR FURTHER INFORMATION CONTACT:
[60Day–21–1314; Docket No. CDC–2021–
0077]
SUMMARY:
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.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
jbell on DSKJLSW7X2PROD with NOTICES
Number of
respondents
Type of respondents
PO 00000
Frm 00096
Fmt 4703
Sfmt 4703
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
Understanding the needs of ovarian
cancer survivors. (OMB Control No.
0920–1314, Exp. 12/31/2021)—
Extension—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Ovarian cancer is the ninth most
common cancer, and the fifth leading
cause of cancer death among women in
the United States. Over 20,000 women
are diagnosed with ovarian cancer each
year. Due to the lack of a recommended
screening test, ovarian cancer is often
diagnosed at late stages, leading to low
five-year survival rates. While previous
studies are able to identify some of the
needs of ovarian cancer survivors,
particularly related to physical
complications and side effects,
additional research is needed to further
understand the experiences and needs
of survivors.
The National Academies of Sciences,
Engineering, and Medicine released
their report, Ovarian Cancers: Evolving
Paradigms in Research and Care, which
identified key priorities for researchers,
including recommending research on
the ‘‘supportive care needs of ovarian
cancer survivors throughout the disease
trajectory.’’ In order to address these
research gaps and supplement current
knowledge of the ongoing needs of
survivors, including how to implement
E:\FR\FM\06AUN1.SGM
06AUN1
43255
Federal Register / Vol. 86, No. 149 / Friday, August 6, 2021 / Notices
programs and interventions to improve
their health, CDC has supported a
survey of ovarian cancer survivors.
The goal of this project is to better
understand the needs of ovarian cancer
survivors and how to more effectively
develop interventions targeted to this
population. To achieve this goal,
multiple recruitment methods will be
utilized to recruit this unique
population of women for the study. By
using state cancer registries, social
media advertisements, and respondentdriven sampling (RDS), the study will
4. What unmet needs do ovarian
cancer survivors have?
The overall sample design targets
1,200 completed interviews. Completed
surveys will come from more traditional
sampling utilizing lists from the state
cancer registries (n = 1,200). This is a
request for an extension of two years to
the data collection period. Participation
in this study is voluntary. The total
estimated annual burden hours are
1,000. There are no costs to respondents
other than their time.
ensure recruit of a diverse population of
women.
This study will focus on the following
research questions:
1. What physical and mental
conditions do ovarian cancer survivors
experience?
2. What kinds of pharmacologic and
non-pharmacologic interventions do
ovarian cancer survivors utilize to
manage their conditions?
3. What barriers do ovarian cancer
survivors have in accessing and
receiving appropriate diagnostic care,
treatment, and follow-up care?
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Ovarian cancer survivors—state cancer registries.
Total ...........................................
Mail-in or web-based questionnaire
...........................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–16825 Filed 8–5–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10653]
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
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
jbell on DSKJLSW7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
19:29 Aug 05, 2021
Number of
respondents
Form name
Jkt 253001
Frm 00097
Fmt 4703
Avg. burden
per response
(in hrs)
Total burden
(in hours)
1,200
1
50/60
1,000
........................
........................
........................
1,000
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
October 5, 2021.
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 https://
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: lll , Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
PO 00000
Number of
responses per
respondent
Sfmt 4703
1. Access CMS’ website address at
https://www.cms.gov/Regulations-andGuidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10653 Coverage of Certain
Preventive Services Under the
Affordable Care Act
Under the 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.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
E:\FR\FM\06AUN1.SGM
06AUN1
]]>Agencies
[Federal Register Volume 86, Number 149 (Friday, August 6, 2021)]
[Notices]
[Pages 43254-43255]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-16825]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-21-1314; Docket No. CDC-2021-0077]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: 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 Understanding
important issues in ovarian cancer survivorship (OCS) project. The OCS
project aims to better understand the needs of ovarian cancer survivors
and how to more effectively develop interventions targeted to this
population.
DATES: CDC must receive written comments on or before October 5, 2021.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2021-
0077 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: 404-639-7118; 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;
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
Understanding the needs of ovarian cancer survivors. (OMB Control
No. 0920-1314, Exp. 12/31/2021)--Extension--National Center for Chronic
Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Ovarian cancer is the ninth most common cancer, and the fifth
leading cause of cancer death among women in the United States. Over
20,000 women are diagnosed with ovarian cancer each year. Due to the
lack of a recommended screening test, ovarian cancer is often diagnosed
at late stages, leading to low five-year survival rates. While previous
studies are able to identify some of the needs of ovarian cancer
survivors, particularly related to physical complications and side
effects, additional research is needed to further understand the
experiences and needs of survivors.
The National Academies of Sciences, Engineering, and Medicine
released their report, Ovarian Cancers: Evolving Paradigms in Research
and Care, which identified key priorities for researchers, including
recommending research on the ``supportive care needs of ovarian cancer
survivors throughout the disease trajectory.'' In order to address
these research gaps and supplement current knowledge of the ongoing
needs of survivors, including how to implement
[[Page 43255]]
programs and interventions to improve their health, CDC has supported a
survey of ovarian cancer survivors.
The goal of this project is to better understand the needs of
ovarian cancer survivors and how to more effectively develop
interventions targeted to this population. To achieve this goal,
multiple recruitment methods will be utilized to recruit this unique
population of women for the study. By using state cancer registries,
social media advertisements, and respondent-driven sampling (RDS), the
study will ensure recruit of a diverse population of women.
This study will focus on the following research questions:
1. What physical and mental conditions do ovarian cancer survivors
experience?
2. What kinds of pharmacologic and non-pharmacologic interventions
do ovarian cancer survivors utilize to manage their conditions?
3. What barriers do ovarian cancer survivors have in accessing and
receiving appropriate diagnostic care, treatment, and follow-up care?
4. What unmet needs do ovarian cancer survivors have?
The overall sample design targets 1,200 completed interviews.
Completed surveys will come from more traditional sampling utilizing
lists from the state cancer registries (n = 1,200). This is a request
for an extension of two years to the data collection period.
Participation in this study is voluntary. The total estimated annual
burden hours are 1,000. There are no costs to respondents other than
their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Avg. burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hrs) (in hours)
----------------------------------------------------------------------------------------------------------------
Ovarian cancer survivors-- Mail-in or web- 1,200 1 50/60 1,000
state cancer registries. based
questionnaire.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 1,000
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2021-16825 Filed 8-5-21; 8:45 am]
BILLING CODE 4163-18-P
