Agency Forms Undergoing Paperwork Reduction Act Review, 6559-6560 [2022-02401]
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6559
Federal Register / Vol. 87, No. 24 / Friday, February 4, 2022 / Notices
estimated that 15 minutes is required for
the next-of-kin to complete this form.
• Authorization for Payment of
Autopsy Form (2.19)—Revised 42 CFR
part 37.204 outlines a need for a
physician pathologist to obtain written
authorization from NIOSH and
agreement regarding payment amount
for services specified in § 37.202 (a) by
completing the Authorization for
Payment of Autopsy form and
submitting it to the CWHSP for
authorization prior to completing an
autopsy on a coal miner. This is a new
form. It will be completed by the
pathologist who intends on conducting
an autopsy and the form will collect:
Demographic information on the
deceased miner, characteristics of the
miner’s pneumoconiosis (if known by
the pathologist), demographic and
medical licensure information from the
requesting pathologist, and proposed
payment amount to complete the
autopsy in accordance with § 37.203. It
is estimated that 15 minutes is required
for the pathologist to complete this
form. The total estimated burden hours
is 11,741.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Coal Mine Operator ........................................
Coal Mine Contractor ......................................
Radiograph Facility Supervisor .......................
Coal Miner .......................................................
Coal Miner—Radiograph ................................
B Reader Physician ........................................
Physicians taking the B Reader Examination
Spirometry Facility Supervisor ........................
Spirometry Facility Employee .........................
Spirometry Technician ....................................
Coal Miner—Spirometry ..................................
Pathologist ......................................................
Pathologist ......................................................
Pathologist ......................................................
Next-of-kin for deceased miner ......................
2.10 ................................................................
2.18 ................................................................
2.11 ................................................................
2.9 ..................................................................
No form required ............................................
2.8 ..................................................................
2.12 ................................................................
2.14 ................................................................
2.13 ................................................................
2.15 ................................................................
No form required ............................................
2.19 ................................................................
Invoice—No standard form ............................
Pathology Report—No standard form ............
2.6 ..................................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–02400 Filed 2–3–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–22–0800]
Agency Forms Undergoing Paperwork
Reduction Act Review
lotter on DSK11XQN23PROD with NOTICES1
No. of
respondents
Type of respondent
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Focus Group
Testing to Effectively Plan and Tailor
Cancer Prevention and Control
Communications Campaigns’’ 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 July 26, 2021 to obtain
comments from the public and affected
agencies. CDC did not receive comments
related to the previous notice. This
notice serves to allow an additional 30
VerDate Sep<11>2014
18:50 Feb 03, 2022
Jkt 256001
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.
PO 00000
Frm 00077
Fmt 4703
Sfmt 4703
220
160
20
8,500
8,500
10
220
15
8,500
8,500
8,500
4
4
4
4
No. of
responses per
respondent
Average
burden per response
(in hours)
1
1
1
1
1
1,760
1
1
1
1
1
1
1
1
1
30/60
30/60
30/60
20/60
15/60
3/60
10/60
30/60
5/60
20/60
15/60
15/60
5/60
5/60
15/60
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
Focus Group Testing to Effectively
Plan and Tailor Cancer Prevention and
Control Communications Campaigns
(OMB Control No. 0920–0800, Exp. 10/
31/2021)—Reinstatement with Change—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The mission of the CDC’s Division of
Cancer Prevention and Control (DCPC)
is to reduce the burden of cancer in the
United States through cancer
prevention, reduction of risk, early
detection, and improved quality of life
E:\FR\FM\04FEN1.SGM
04FEN1
6560
Federal Register / Vol. 87, No. 24 / Friday, February 4, 2022 / Notices
for cancer survivors. Toward this end,
the DCPC supports the scientific
development and implementation of
various health communication
campaigns with an emphasis on specific
cancer burdens.
This process requires testing of
messages, concepts, and materials prior
to their final development and
dissemination, as described in the
second step of the health
communication process. The health
communication process is a scientific
model developed by the U.S.
Department of Health and Human
Services’ National Cancer Institute to
guide sound campaign development.
The communication literature supports
various data collection methods to
conduct credible formative, concept,
message, and materials testing. This
process ensures that the public clearly
understands cancer-specific information
and concepts, are motivated to take the
desired action, and do not react
negatively to the messages. CDC was
previously approved to collect
information needed to plan and tailor
cancer communication campaigns (OMB
Control No. 0920–0800, Exp. 10/31/
2021), and seeks OMB approval to
revise the existing generic clearance to
include another cancer-related
communications campaign, expand the
modes of data collection to include
online focus groups and in-depth
interviews (in-person, phone, and
online), and to focus on respondents
from the general public.
Information collection will involve
discussions to assess numerous
qualitative dimensions of cancer
prevention and control messages,
including but not limited to, cancer
knowledge, attitudes, beliefs, behavioral
intentions, information needs and
sources, and compliance with cancer
screening as recommended by the
United States Preventive Services Task
Force. Insights gained from these
discussions will assist in the
development and/or refinement of
future campaign messages and
materials. Communication campaigns
and messages will vary according to the
type of cancer and the qualitative
dimensions of the message described
above.
A separate information collection
request will be submitted to OMB for
approval of each discussion activity.
The request will describe the purpose of
the activity and include the customized
information collection instruments.
OMB approval is requested for three
years. CDC requests OMB approval for
an estimated 1,680 annual burden
hours. Participation is voluntary and
there are no costs to respondents except
their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
General Public ................................................
General Public ................................................
Screening Form ..............................................
Discussion Guide ...........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–02401 Filed 2–3–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
CDC must receive written
comments on or before April 5, 2022.
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 efforts 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 a proposed and/or
continuing information collection, as
VerDate Sep<11>2014
18:50 Feb 03, 2022
Jkt 256001
You may submit comments,
identified by Docket No. CDC–2022–
0017 by any of the following methods:
• Federal eRulemaking Portal:
regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffery 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
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
ADDRESSES:
Extension of Existing Collection of
Information Submitted for Public
Comment and Recommendations
SUMMARY:
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on the extension of an existing
collection of information titled
Assessment of Outcomes Associated
with the Preventive Health and Health
Services Block Grant. This assessment
will assess select cross-cutting outputs
and outcomes of the Preventive Health
and Health Services Block Grant and
demonstrate the utility of the grant on
a national level.
DATES:
[60Day–22–1257; Docket No. CDC–2022–
0017]
lotter on DSK11XQN23PROD with NOTICES1
Number of
respondents
Type of respondents
PO 00000
Frm 00078
Fmt 4703
Sfmt 4703
1,600
800
Number of
responses per
respondent
Average
burden per
response
(in hours)
1
1
3/60
2
(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 Jeffery M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, H21–
8, Atlanta, Georgia 30329; phone: 404–
639–7570; Email: omb@cdc.gov.
FOR FURTHER INFORMATION CONTACT:
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.
SUPPLEMENTARY INFORMATION:
E:\FR\FM\04FEN1.SGM
04FEN1
]]>Agencies
[Federal Register Volume 87, Number 24 (Friday, February 4, 2022)]
[Notices]
[Pages 6559-6560]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-02401]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-22-0800]
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 ``Focus Group Testing to Effectively Plan and
Tailor Cancer Prevention and Control Communications Campaigns'' 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 July 26, 2021 to obtain
comments from the public and affected agencies. CDC did not receive
comments related to the previous notice. This notice serves to allow an
additional 30 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
Focus Group Testing to Effectively Plan and Tailor Cancer
Prevention and Control Communications Campaigns (OMB Control No. 0920-
0800, Exp. 10/31/2021)--Reinstatement with Change--National Center for
Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The mission of the CDC's Division of Cancer Prevention and Control
(DCPC) is to reduce the burden of cancer in the United States through
cancer prevention, reduction of risk, early detection, and improved
quality of life
[[Page 6560]]
for cancer survivors. Toward this end, the DCPC supports the scientific
development and implementation of various health communication
campaigns with an emphasis on specific cancer burdens.
This process requires testing of messages, concepts, and materials
prior to their final development and dissemination, as described in the
second step of the health communication process. The health
communication process is a scientific model developed by the U.S.
Department of Health and Human Services' National Cancer Institute to
guide sound campaign development. The communication literature supports
various data collection methods to conduct credible formative, concept,
message, and materials testing. This process ensures that the public
clearly understands cancer-specific information and concepts, are
motivated to take the desired action, and do not react negatively to
the messages. CDC was previously approved to collect information needed
to plan and tailor cancer communication campaigns (OMB Control No.
0920-0800, Exp. 10/31/2021), and seeks OMB approval to revise the
existing generic clearance to include another cancer-related
communications campaign, expand the modes of data collection to include
online focus groups and in-depth interviews (in-person, phone, and
online), and to focus on respondents from the general public.
Information collection will involve discussions to assess numerous
qualitative dimensions of cancer prevention and control messages,
including but not limited to, cancer knowledge, attitudes, beliefs,
behavioral intentions, information needs and sources, and compliance
with cancer screening as recommended by the United States Preventive
Services Task Force. Insights gained from these discussions will assist
in the development and/or refinement of future campaign messages and
materials. Communication campaigns and messages will vary according to
the type of cancer and the qualitative dimensions of the message
described above.
A separate information collection request will be submitted to OMB
for approval of each discussion activity. The request will describe the
purpose of the activity and include the customized information
collection instruments. OMB approval is requested for three years. CDC
requests OMB approval for an estimated 1,680 annual burden hours.
Participation is voluntary and there are no costs to respondents except
their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondents Form name respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
General Public........................ Screening Form.......... 1,600 1 3/60
General Public........................ Discussion Guide........ 800 1 2
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-02401 Filed 2-3-22; 8:45 am]
BILLING CODE 4163-18-P
