Agency Forms Undergoing Paperwork Reduction Act Review, 18595 [2013-07041]
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18595
Federal Register / Vol. 78, No. 59 / Wednesday, March 27, 2013 / Notices
Dated: March 21, 2013.
Ben O’Dell,
Associate Director for Center for Faith-based
and Neighborhood Partnerships at U.S.
Department of Health and Human Services.
[FR Doc. 2013–07142 Filed 3–26–13; 8:45 am]
BILLING CODE 4154–07–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day-13–0745]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Colorectal Cancer Screening Program
(OMB No. 0920–0745, exp. 6/30/2013)—
Extension—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Of cancers affecting both men and
women, colorectal cancer (CRC) is the
second leading cause of cancer-related
deaths in the United States. Based on
scientific evidence which indicates that
regular screening is effective in reducing
CRC incidence and mortality, regular
CRC screening is now recommended for
adults starting at age 50 and continuing
until age 75 years.
In 2005, CDC established a three-year
demonstration program, subsequently
extended to four years, to screen lowincome individuals 50 years of age and
older who have no health insurance or
inadequate health insurance for CRC.
The five demonstration sites reported
information to CDC including deidentified, patient-level demographic,
screening, diagnostic, treatment,
outcome and cost reimbursement data
(OMB No. 0920–0745, exp. 7/31/2010).
The information has been used to assess
the feasibility and cost effectiveness of
a publically funded screening program,
describe key outcomes, and guide the
expansion of the program. In 2009, with
the conclusion of the demonstration
program and increased Congressional
funding to continue support of a
colorectal cancer screening program,
CDC established the Colorectal Cancer
Control Program (CRCCP) to fund 26
sites for a five-year program period to
increase population-based CRC
screening and reduce health disparities
in CRC screening, incidence and
mortality. Funded sites implement
evidence-based interventions to increase
population-level screening rates. To
address disparities in access to
screening, funded sites screen lowincome individuals 50 years of age and
older who have no health insurance or
inadequate health insurance for CRC.
The funded sites report information to
CDC including programmatic-level
activity cost data, and de-identified
patient-level demographic, screening,
diagnostic, treatment and outcome data
(OMB No. 0920–0745, exp. 6/30/2013).
CDC is requesting OMB approval to
continue the information collection for
an additional three years. CDC will
collect de-identified Colorectal Clinical
Data Elements (CCDE) on services
provided to low-income individuals age
50 and older with inadequate or no
health insurance. CDC will use the
information to monitor and evaluate the
program and funded sites; improve the
quality of screening and diagnostic
services for underserved individuals;
develop outreach strategies to increase
screening; and report program results to
Congress and other legislative
authorities. Each site will screen an
estimated 375 individuals per year (186
semiannually).
The program will also collect
program-level activity-based cost data
utilizing a Cost Assessment Tool (CAT)
previously used by other CDC-funded
cancer programs. The information to be
collected through the CAT will allow
CDC to compare activity-based costs
across multiple sites and programs, and
will provide a more effective means of
monitoring and improving the
performance and cost-effectiveness of
the CRC screening program.
Summary CCDE information will be
transmitted to CDC electronically twice
per year. Information collected through
the Cost Assessment Tool will be
transmitted electronically to CDC once
per year. Participation is required for all
sites funded through the CRC screening
program. The number of funded sites
will increase from 26 to 29 and this will
result in an increase in the number of
respondents and total burden. There are
no changes to the content of the
information collection or the estimated
burden per response.
There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
3,357.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Colorectal Cancer Screening Programs .........
mstockstill on DSK4VPTVN1PROD with NOTICES
Type of respondents
Clinical Data Elements ...................................
Cost Assessment Tool ...................................
Number of
responses per
respondent
29
29
Dated: March 21, 2013.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI),
Office of the Associate Director for Science
(OADS), Office of the Director, Centers for
Disease Control and Prevention.
[FR Doc. 2013–07041 Filed 3–26–13; 8:45 am]
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Avg. burden
per response
(in hours)
15/60
22
Agencies
[Federal Register Volume 78, Number 59 (Wednesday, March 27, 2013)]
[Notices]
[Page 18595]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-07041]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-13-0745]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-7570 or send an email to
omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-5806.
Written comments should be received within 30 days of this notice.
Proposed Project
Colorectal Cancer Screening Program (OMB No. 0920-0745, exp. 6/30/
2013)--Extension--National Center for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
Of cancers affecting both men and women, colorectal cancer (CRC) is
the second leading cause of cancer-related deaths in the United States.
Based on scientific evidence which indicates that regular screening is
effective in reducing CRC incidence and mortality, regular CRC
screening is now recommended for adults starting at age 50 and
continuing until age 75 years.
In 2005, CDC established a three-year demonstration program,
subsequently extended to four years, to screen low-income individuals
50 years of age and older who have no health insurance or inadequate
health insurance for CRC. The five demonstration sites reported
information to CDC including de-identified, patient-level demographic,
screening, diagnostic, treatment, outcome and cost reimbursement data
(OMB No. 0920-0745, exp. 7/31/2010). The information has been used to
assess the feasibility and cost effectiveness of a publically funded
screening program, describe key outcomes, and guide the expansion of
the program. In 2009, with the conclusion of the demonstration program
and increased Congressional funding to continue support of a colorectal
cancer screening program, CDC established the Colorectal Cancer Control
Program (CRCCP) to fund 26 sites for a five-year program period to
increase population-based CRC screening and reduce health disparities
in CRC screening, incidence and mortality. Funded sites implement
evidence-based interventions to increase population-level screening
rates. To address disparities in access to screening, funded sites
screen low-income individuals 50 years of age and older who have no
health insurance or inadequate health insurance for CRC. The funded
sites report information to CDC including programmatic-level activity
cost data, and de-identified patient-level demographic, screening,
diagnostic, treatment and outcome data (OMB No. 0920-0745, exp. 6/30/
2013).
CDC is requesting OMB approval to continue the information
collection for an additional three years. CDC will collect de-
identified Colorectal Clinical Data Elements (CCDE) on services
provided to low-income individuals age 50 and older with inadequate or
no health insurance. CDC will use the information to monitor and
evaluate the program and funded sites; improve the quality of screening
and diagnostic services for underserved individuals; develop outreach
strategies to increase screening; and report program results to
Congress and other legislative authorities. Each site will screen an
estimated 375 individuals per year (186 semiannually).
The program will also collect program-level activity-based cost
data utilizing a Cost Assessment Tool (CAT) previously used by other
CDC-funded cancer programs. The information to be collected through the
CAT will allow CDC to compare activity-based costs across multiple
sites and programs, and will provide a more effective means of
monitoring and improving the performance and cost-effectiveness of the
CRC screening program.
Summary CCDE information will be transmitted to CDC electronically
twice per year. Information collected through the Cost Assessment Tool
will be transmitted electronically to CDC once per year. Participation
is required for all sites funded through the CRC screening program. The
number of funded sites will increase from 26 to 29 and this will result
in an increase in the number of respondents and total burden. There are
no changes to the content of the information collection or the
estimated burden per response.
There are no costs to respondents other than their time. The total
estimated annualized burden hours are 3,357.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Avg. burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Colorectal Cancer Screening Programs.. Clinical Data Elements.. 29 375 15/60
Cost Assessment Tool.... 29 1 22
----------------------------------------------------------------------------------------------------------------
Dated: March 21, 2013.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI), Office of the Associate
Director for Science (OADS), Office of the Director, Centers for
Disease Control and Prevention.
[FR Doc. 2013-07041 Filed 3-26-13; 8:45 am]
BILLING CODE 4163-18-P