Agency Forms Undergoing Paperwork Reduction Act Review, 16016-16018 [2015-06929]
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16016
Federal Register / Vol. 80, No. 58 / Thursday, March 26, 2015 / Notices
Estimates of Annualized Hour Burden
The estimated annualized burden for
a uniform application is 37,429 hours.
Burden estimates are broken out in the
following tables showing burden
separately for Year 1 and Year 2. Year
1 includes the estimates of burden for
the uniform application and annual
reporting. Year 2 includes the estimates
of burden for the application update and
annual reporting. The reporting burden
remains constant for both years.
TABLE 1—ESTIMATES OF APPLICATION AND REPORTING BURDEN FOR YEAR 1
Application element
Burden/
response
(hours)
Responses/
respondents
Number respondents
Total burden
Application Burden
Yr One Plan (separate submissions) ..............
1
282
16,920
Yr One Plan (combined submission ...............
30 (CMHS) .....................................................
30 (SAPT) ......................................................
30 ...................................................................
1
282
8,460
Application Sub-total ................................
60 ...................................................................
........................
........................
25,380
Reporting Burden
MHBG Report .................................................
URS Tables .....................................................
SAPTBG Report ..............................................
Table 5 ............................................................
59 ...................................................................
59 ...................................................................
60 1 .................................................................
15 2 .................................................................
1
1
1
1
186
35
186
4
10,974
2,065
11,160
60
Reporting Subtotal ...................................
60 ...................................................................
........................
........................
24,259
Total ..................................................
119 .................................................................
........................
........................
49,639
1 Redlake
2 Only
Band of the Chippewa Indians from MN receives a grant.
15 States have a management information system to complete Table 5.
TABLE 2—ESTIMATES OF APPLICATION AND REPORTING BURDEN FOR YEAR 2
Application element
Burden/
response
(hours)
Responses/
respondents
Number respondents
Total burden
Application Burden
Yr Two Plan ....................................................
24 ...................................................................
1
40
960
Application Sub-total ................................
24 ...................................................................
........................
........................
960
...................................................................
...................................................................
...................................................................
...................................................................
1
1
1
1
186
35
186
4
10,974
2,065
11,160
60
Reporting Subtotal ...................................
60 ...................................................................
........................
........................
24,259
Total ..................................................
119 .................................................................
........................
........................
25,219
Reporting Burden
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MHBG Report .................................................
URS Tables .....................................................
SAPTBG Report ..............................................
Table 5 ............................................................
The total annualized burden for the
application and reporting is 37,429
hours (49,639 + 25,219 = 74,858/2 years
= 37,429).
Link for the application: https://www.
samhsa.gov/grants/block-grants.
Written comments and
recommendations concerning the
proposed information collection should
be sent by April 27, 2015 to the
SAMHSA Desk Officer at the Office of
Information and Regulatory Affairs,
Office of Management and Budget
(OMB). To ensure timely receipt of
comments, and to avoid potential delays
in OMB’s receipt and processing of mail
sent through the U.S. Postal Service,
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59
59
60
15
commenters are encouraged to submit
their comments to OMB via email to:
OIRA_Submission@omb.eop.gov.
Although commenters are encouraged to
send their comments via email,
commenters may also fax their
comments to: 202–395–7285.
Commenters may also mail them to:
Office of Management and Budget,
Office of Information and Regulatory
Affairs, New Executive Office Building,
Room 10102, Washington, DC 20503.
Summer King,
Statistician.
[FR Doc. 2015–06915 Filed 3–25–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–15–0963]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
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16017
Federal Register / Vol. 80, No. 58 / Thursday, March 26, 2015 / Notices
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (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 or
send an email to omb@cdc.gov. Written
comments and/or suggestions regarding
the items contained in this notice
should be directed to the Attention:
CDC Desk Officer, Office of Management
and Budget, Washington, DC 20503 or
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Colorectal Cancer Control Program
Indirect/Non-Medical Cost Study (OMB
No. 0920–0963, exp. 4/30/2014)—
Reinstatement—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Colorectal Cancer (CRC) is the second
leading cause of cancer-related deaths in
the United States, following lung
cancer. Regular CRC screening is now
recommended for average-risk persons.
While screening rates have increased
over the past decade, screening
prevalence is still lower than desirable,
particularly among individuals with low
socioeconomic status. In 2009, the
Centers for Disease Control and
Prevention (CDC) designed and initiated
the population-based Colorectal Cancer
Control Program (CRCCP) at 29 sites.
The goals of the program are to reduce
health disparities in CRC screening,
incidence and mortality by promoting
CRC screening for the eligible
population and providing CRC
screening to low-income adults over 50
years of age who have no health
insurance or inadequate health
insurance for CRC screening.
In 2013 CDC received Office of
Management and Budget (OMB)
approval to conduct a study to measure
the time and costs incurred by patients
screened for CRC (OMB No. 0920–0963,
exp. 4/30/2014). Understanding the
indirect and non-medical costs
associated with CRC screening may
provide insights on the barriers to
screening participation. Information has
been collected, however, the target
number of respondents was not
achieved during the initial approval
period. CDC requests OMB approval to
reinstate the information collection for
one year in order to meet recruitment
goals and complete the data analysis as
outlined in the original approval.
Information will be collected from a
subset of patients enrolled in the
CRCCP. Those who undergo screening
by FIT or colonoscopy will be asked to
complete a specialized questionnaire
about the time and personal expense
associated with their screening. The FIT
questionnaire is estimated to take about
10 minutes. The Colonoscopy
questionnaire, which includes
additional questions about the
preparation and recovery associated
with this procedure, has an estimated
burden per response of 25 minutes.
Demographic information will be
collected from all patients who
participate in the study.
CDC plans to conduct the information
collection in partnership with providers
in four states (Alabama, Arizona,
Georgia, and Pennsylvania). Providers
will be reimbursed for patient navigator
time and administrative expense
associated with data collection.
The target number of responses for the
overall study will result in 300
completed Colonoscopy Questionnaires
and 290 completed FIT Questionnaires.
To complete the study CDC plans to
collect an additional 150 Colonoscopy
Questionnaires and an additional 177
FIT Questionnaires.
This information collection will be
used to produce estimates of the
personal costs incurred by patients who
undergo CRC screening by FIT or
colonoscopy, and to improve
understanding of these costs as potential
barriers to participation. Study findings
will be disseminated through reports,
presentations, and publications. Results
will also be used by participating sites,
CDC, and other federal agencies to
improve delivery of CRC screening
services and to increase screening rates
among low-income adults over 50 years
of age who have no health insurance or
inadequate health insurance for CRC
screening.
OMB approval is requested for one
year. Each respondent will have the
option of completing a hardcopy
questionnaire or an on-line
questionnaire. No identifiable
information will be collected by CDC or
CDC’s data collection contractor.
Participation is voluntary and there are
no costs to respondents other than their
time. The total estimated annualized
burden hours are 93.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form type
Patients Served by the Colorectal Cancer
Control Program.
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Type of respondent
FIT questionnaire .....................................
Colonoscopy questionnaire ......................
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Number of
responses per
respondent
177
150
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Average rurden
per response
(in hours)
1
1
26MRN1
10/60
25/60
16018
Federal Register / Vol. 80, No. 58 / Thursday, March 26, 2015 / Notices
Leroy A. Richardson,
Chief, 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. 2015–06929 Filed 3–25–15; 8:45 am]
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DEPARTMENT OF HOMELAND
SECURITY
[Docket ID FEMA–2015–0006]
Notice To Extend the Comment Period
for the Proposed Revised Guidelines
for Implementing Executive Order
11988, Floodplain Management, as
Revised Through the Federal Flood
Risk Management Standard
Federal Emergency
Management Agency, DHS.
ACTION: Notice.
AGENCY:
This notice extends the
comment period for the proposed
‘‘Revised Guidelines for Implementing
Executive Order 11988, Floodplain
Management’’ published in the Federal
Register on February 5, 2015 (80 FR
6530). The comment period for the
proposed revised guidelines, which
would have ended on April 6, 2015, is
extended for 30 days.
DATES: The comment period is extended
until May 6, 2015.
ADDRESSES: Comments must be
identified by docket ID FEMA–2015–
0006 and may be submitted by one of
the following methods:
Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Mail/Hand Delivery/Courier:
Regulatory Affairs Division, Office of
Chief Counsel, Federal Emergency
Management Agency, 8NE, 500 C Street
SW., Washington, DC 20472–3100.
Instructions: All submissions received
must include the docket ID FEMA–
2015–0006. Comments received will be
posted without alteration at https://
www.regulations.gov, including any
personal information provided.
Docket: For access to the docket to
read comments received, go to https://
www.regulations.gov, and search for the
Docket ID FEMA–2015–0006.
Background Information: Background
information about these topics is
available on the FFRMS Web site at
https://www.fema.gov/federal-floodrisk-management-standard-ffrms or in
the docket for this Notice at
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FOR FURTHER INFORMATION CONTACT:
Bradley Garner, 202–646–3901 or
FEMA-FFRMS@fema.dhs.gov. Mailing
Address: FFRMS, 1800 South Bell
Street, Room 627, Arlington, VA 20598–
3030. The Web site is https://www.fema.
gov/federal-flood-risk-managementstandard-ffrms.
On
January 30, 2015, the President signed
Executive Order 13690, directing FEMA,
on behalf of the Mitigation Framework
Leadership Group, to publish for public
comment draft revised Floodplain
Management Guidelines to provide
guidance to agencies on the
implementation of Executive Order
11988, as amended, consistent with a
new Federal Flood Risk Management
Standard. These draft revised
Guidelines were developed by the
Mitigation Framework Leadership
Group in consultation with the Federal
Interagency Floodplain Management
Task Force. On February 5, 2015, FEMA
published the proposed ‘‘Revised
Guidelines for Implementing Executive
Order 11988, Floodplain Management’’
on behalf of the Mitigation Framework
Leadership Group to solicit and
consider public input.
The Mitigation Framework
Leadership Group has received several
comments regarding the 60-day time
period to submit comments. The
commenters stated that they needed
additional time to review and
adequately respond to the proposed
revised guidelines because of the
complex nature of the topic. Because of
the scope of the proposed revised
guidelines, and because the Mitigation
Framework Leadership Group has
specifically requested the public’s
comments on the proposed revised
guidelines in an attempt to benefit from
the experience of all interested parties,
the comment period will be extended
for an additional 30 days. This notice
announces the extension of the public
comment period to May 6, 2015.
SUPPLEMENTARY INFORMATION:
Federal Emergency Management
Agency
SUMMARY:
www.regulations.gov, Docket ID FEMA–
2015–0006.
Authority: Executive Order 11988, as
amended; Executive Order 13690.
DEPARTMENT OF THE INTERIOR
Bureau of Land Management
[LLIDT000000.L11200000.DD0000.241A.00;
4500069133]
Notice of Public Meetings, Twin Falls
District Resource Advisory Council,
Idaho
AGENCY:
Bureau of Land Management,
Interior.
ACTION:
Notice of public meetings.
In accordance with the
Federal Land Policy and Management
Act (FLPMA), the Federal Advisory
Committee Act of 1972 (FACA), the U.S.
Department of the Interior, Bureau of
Land Management (BLM) Twin Falls
District Resource Advisory Council
(RAC) will meet as indicated below.
SUMMARY:
The Twin Falls District RAC will
meet April 22, 2015, at the Sawtooth
Best Western Inn, 2653 S. Lincoln
Avenue, Jerome, Idaho 83338. The
meeting will begin at 9:00 a.m. and end
no later than 3:00 p.m. The public
comment period will take place from
9:10 a.m. to 9:40 a.m.
DATES:
FOR FURTHER INFORMATION CONTACT:
Heather Tiel-Nelson, Twin Falls
District, Idaho, 2536 Kimberly Road,
Twin Falls, Idaho 83301, (208) 736–
2352.
The 15member RAC advises the Secretary of
the Interior, through the Bureau of Land
Management, on a variety of planning
and management issues associated with
public land management in Idaho.
During the April 22nd meeting, there
will be an overview of the roles and
responsibilities of a BLM manager, an
update on the Idaho and Southwest
Montana Sub-regional Sage-Grouse Draft
Environmental Impact Statement, and
field office updates. Additional topics
may be added and will be included in
local media announcements.
More information is available at
www.blm.gov/id/st/en/res/resource_
advisory.3.html. RAC meetings are open
to the public.
SUPPLEMENTARY INFORMATION:
Roy Wright,
Deputy Associate Administrator for
Mitigation, Federal Emergency Management
Agency.
Elizabeth Maclean,
BLM Twin Falls District Manager (Acting).
[FR Doc. 2015–06879 Filed 3–25–15; 8:45 am]
[FR Doc. 2015–06912 Filed 3–25–15; 8:45 am]
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Authority: 43 CFR 1784.4–1.
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Agencies
[Federal Register Volume 80, Number 58 (Thursday, March 26, 2015)]
[Notices]
[Pages 16016-16018]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-06929]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-15-0963]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has submitted
the following information collection request to the Office of
Management and Budget (OMB) for review and approval in accordance with
the Paperwork Reduction Act of 1995. The notice for
[[Page 16017]]
the proposed information collection is published to obtain comments
from the public and affected agencies.
Written comments and suggestions from the public and affected
agencies concerning the proposed collection of information are
encouraged. Your comments should address any of the following: (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 or send an email to omb@cdc.gov. Written comments and/or
suggestions regarding the items contained in this notice should be
directed to the Attention: CDC Desk Officer, Office of Management and
Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written
comments should be received within 30 days of this notice.
Proposed Project
Colorectal Cancer Control Program Indirect/Non-Medical Cost Study
(OMB No. 0920-0963, exp. 4/30/2014)--Reinstatement--National Center for
Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Colorectal Cancer (CRC) is the second leading cause of cancer-
related deaths in the United States, following lung cancer. Regular CRC
screening is now recommended for average-risk persons. While screening
rates have increased over the past decade, screening prevalence is
still lower than desirable, particularly among individuals with low
socioeconomic status. In 2009, the Centers for Disease Control and
Prevention (CDC) designed and initiated the population-based Colorectal
Cancer Control Program (CRCCP) at 29 sites. The goals of the program
are to reduce health disparities in CRC screening, incidence and
mortality by promoting CRC screening for the eligible population and
providing CRC screening to low-income adults over 50 years of age who
have no health insurance or inadequate health insurance for CRC
screening.
In 2013 CDC received Office of Management and Budget (OMB) approval
to conduct a study to measure the time and costs incurred by patients
screened for CRC (OMB No. 0920-0963, exp. 4/30/2014). Understanding the
indirect and non-medical costs associated with CRC screening may
provide insights on the barriers to screening participation.
Information has been collected, however, the target number of
respondents was not achieved during the initial approval period. CDC
requests OMB approval to reinstate the information collection for one
year in order to meet recruitment goals and complete the data analysis
as outlined in the original approval.
Information will be collected from a subset of patients enrolled in
the CRCCP. Those who undergo screening by FIT or colonoscopy will be
asked to complete a specialized questionnaire about the time and
personal expense associated with their screening. The FIT questionnaire
is estimated to take about 10 minutes. The Colonoscopy questionnaire,
which includes additional questions about the preparation and recovery
associated with this procedure, has an estimated burden per response of
25 minutes. Demographic information will be collected from all patients
who participate in the study.
CDC plans to conduct the information collection in partnership with
providers in four states (Alabama, Arizona, Georgia, and Pennsylvania).
Providers will be reimbursed for patient navigator time and
administrative expense associated with data collection.
The target number of responses for the overall study will result in
300 completed Colonoscopy Questionnaires and 290 completed FIT
Questionnaires. To complete the study CDC plans to collect an
additional 150 Colonoscopy Questionnaires and an additional 177 FIT
Questionnaires.
This information collection will be used to produce estimates of
the personal costs incurred by patients who undergo CRC screening by
FIT or colonoscopy, and to improve understanding of these costs as
potential barriers to participation. Study findings will be
disseminated through reports, presentations, and publications. Results
will also be used by participating sites, CDC, and other federal
agencies to improve delivery of CRC screening services and to increase
screening rates among low-income adults over 50 years of age who have
no health insurance or inadequate health insurance for CRC screening.
OMB approval is requested for one year. Each respondent will have
the option of completing a hardcopy questionnaire or an on-line
questionnaire. No identifiable information will be collected by CDC or
CDC's data collection contractor. Participation is voluntary and there
are no costs to respondents other than their time. The total estimated
annualized burden hours are 93.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average rurden
Type of respondent Form type Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Patients Served by the Colorectal FIT questionnaire.... 177 1 10/60
Cancer Control Program. Colonoscopy 150 1 25/60
questionnaire.
----------------------------------------------------------------------------------------------------------------
[[Page 16018]]
Leroy A. Richardson,
Chief, 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. 2015-06929 Filed 3-25-15; 8:45 am]
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