Agency Forms Undergoing Paperwork Reduction Act Review, 17921-17922 [2010-7916]
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17921
Federal Register / Vol. 75, No. 67 / Thursday, April 8, 2010 / Notices
maintain contact information for NHSC
Alumni, allow NHSC Alumni to better
communicate with each other, and
enable the Bureau to communicate with
NHSC Alumni (e.g., send updates, plan
meetings, and provide monthly
newsletters).
Basic contact information would be
collected from the NHSC Alumni, such
as, name, state (of residence and/or
employment), contact telephone
number, contact e-mail address,
discipline, specialty, uniformed services
rank and status (active duty or retired),
and NHSC service category (Scholar,
Number of
respondents
Instrument
Alumni Database ..................................................................
E-mail comments to
paperwork@hrsa.gov or mail the HRSA
Reports Clearance Officer, Room 10–33,
Parklawn Building, 5600 Fishers Lane,
Rockville, MD 20857. Written comments
should be received within 60 days of
this notice.
Dated: March 31, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2010–7927 Filed 4–7–10; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30-Day–10–0745]
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) 639–5960 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
sroberts on DSKD5P82C1PROD with NOTICES
Colorectal Cancer Screening Program
(OMB No. 0920–0745 7/31/2010)—
Responses
per
respondent
5,000
Loan Repayor, or Volunteer). The data
would be easily collected and accessed
through a secure Web portal and allow
for the safe collection and storage of this
information.
The estimated annual burden is as
follows:
Total
responses
1
Revision—Division of Cancer
Prevention and Control (DCPC),
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. Based on scientific evidence
which indicates that regular screening is
effective in reducing CRC incidence and
mortality, regular CRC screening is now
recommended for average-risk persons.
In 2005, CDC established a
demonstration program 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 have
reported information to CDC including
de-identified, patient-level
demographic, screening, diagnostic,
treatment, outcome and cost
reimbursement data (Colorectal Cancer
Screening Demonstration Program, OMB
No. 0920–0745, exp. 7/31/2010).
CDC requests OMB approval to
continue the information collection for
three years, with changes. First, the
number of funded sites will increase
from 5 to 26, and the term
‘‘Demonstration’’ will be deleted from
the title. Second, there will be a
reduction in the burden per respondent
associated with the collection of clinical
information. Reporting forms for
medical complications and medically
ineligible clients will be discontinued,
the level of detail collected from
endoscopy and pathology reports will
be reduced, and the reporting form for
colorectal cancer clinical data elements
5,000
Hours per
response
.20
Total burden
hours
1,000
(CCDE) will be streamlined. As a result,
the reporting burden per CCDE form
will be similar regardless of primary test
provided. Third, the collection of
patient-level reimbursement cost data
will be discontinued and will be
replaced by the collection of programlevel activity-based cost data using a
Cost Assessment Tool (CAT). 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 costeffectiveness of the CRC screening
program.
Each program site will screen an
estimated 375 patients per year. Deidentified CCDE information concerning
approximately 187 new screening
records 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.
Reporting is required for all sites funded
through the CRC screening program.
The goals of the expanded CRC
screening program are to increase
population-based screening and to
reduce health disparities in CRC
screening, incidence and mortality. The
program will continue to provide
services to low-income individuals age
50 and older with inadequate or no
health insurance for CRC.
The total estimated annualized
burden hours are 3,010. The increase in
the number of funded sites and the
proposed changes will result in an
overall increase in burden to
respondents. There are no costs to
respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
No. of
respondents
Type of respondents
Form type
Colorectal Cancer Screening Programs .........
Clinical Data Elements ...................................
VerDate Nov<24>2008
18:22 Apr 07, 2010
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26
08APN1
No. of responses per
respondent
375
Average
burden per
response
(in hours)
15/60
17922
Federal Register / Vol. 75, No. 67 / Thursday, April 8, 2010 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Type of respondents
Cost Assessment Tool ...................................
Dated: March 31, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2010–7916 Filed 4–7–10; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–0920–0457]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–5960 and
send comments to Maryam I. Daneshvar,
CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an e-mail to
omb@cdc.gov.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
Average
burden per
response
(in hours)
No. of responses per
respondent
No. of
respondents
Form type
26
1
22
latent tuberculosis infection. In 2000,
CDC implemented two program
evaluation reports for annual
submission: Aggregate report of followup for contacts of tuberculosis, and
aggregate report of screening and
preventive therapy for tuberculosis
infection (OMB No. 0920–0457). The
respondents for these reports are the 68
state and local tuberculosis control
programs receiving federal cooperative
agreement funding through DTBE.
These reports emphasize treatment
outcomes, high-priority target
populations vulnerable to tuberculosis,
and programmed electronic report entry,
which will be transitioned to the
National Tuberculosis Indicators Project
(NTIP), a secure Web-based system for
program evaluation data, in 2010. No
other federal agency collects this type of
national tuberculosis data, and the
aggregate report of follow-up for
contacts of tuberculosis, and aggregate
report of screening and preventive
therapy for tuberculosis infection are
the only data source about latent
tuberculosis infection for monitoring
national progress toward tuberculosis
elimination with these activities. CDC
provides ongoing assistance in the
preparation and utilization of these
reports at the local and state levels of
public health jurisdiction. CDC also
provides respondents with technical
support for the NTIP software
(Electronic—100%, Use of Electronic
Signatures—No). There is no cost to
respondents.
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
Aggregate Reports for Tuberculosis
Program Evaluation (OMB No. 0920–
0457 exp. 5/31/2010)—Reinstatement—
National Center for HIV/AIDS, Viral
Hepatitis, STD, and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
CDC requests the reinstatement of the
Aggregate Reports for Tuberculosis
Program Evaluation, previously
approved under OMB No. 0920–0457
after the 5/31/2010 expiration date, for
3 years. There are no revisions to the
report forms, data definitions, or
reporting instructions.
To ensure the elimination of
tuberculosis in the United States, CDC
monitors indicators for key program
activities, such as finding tuberculosis
infections in recent contacts of cases
and in other persons likely to be
infected and providing therapy for
ESTIMATED ANNUALIZED BURDEN HOURS
sroberts on DSKD5P82C1PROD with NOTICES
Targeted Testing and Treatment for Latent Tuberculosis Infection.
VerDate Nov<24>2008
18:24 Apr 07, 2010
Response format
68 data clerks .......................
50 Electronic .........................
18 Manual .............................
1
1
30/60
3
34
204
50 Electronic .........................
18 Manual .............................
1
1
30/60
30/60
34
34
68 data clerks .......................
50 Electronic .........................
18 Manual .............................
1
1
30/60
3
34
204
68 program managers ..........
Follow-up and Treatment of
Contacts to Tuberculosis
Cases.
Respondents
(state and local tuberculosis
control programs)
68 program managers ..........
Report name
50 Electronic .........................
18 Manual .............................
1
1
30/60
30/60
34
34
Jkt 220001
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PO 00000
Frm 00027
Sfmt 4703
No. response
per
respondent
E:\FR\FM\08APN1.SGM
08APN1
Hours per
response
Total burden
(in hours)
]]>Agencies
[Federal Register Volume 75, Number 67 (Thursday, April 8, 2010)]
[Notices]
[Pages 17921-17922]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-7916]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30-Day-10-0745]
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) 639-5960 or send an e-mail
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 7/31/2010)--
Revision--Division of Cancer Prevention and Control (DCPC), 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. Based on
scientific evidence which indicates that regular screening is effective
in reducing CRC incidence and mortality, regular CRC screening is now
recommended for average-risk persons.
In 2005, CDC established a demonstration program 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 have reported information to CDC including de-
identified, patient-level demographic, screening, diagnostic,
treatment, outcome and cost reimbursement data (Colorectal Cancer
Screening Demonstration Program, OMB No. 0920-0745, exp. 7/31/2010).
CDC requests OMB approval to continue the information collection
for three years, with changes. First, the number of funded sites will
increase from 5 to 26, and the term ``Demonstration'' will be deleted
from the title. Second, there will be a reduction in the burden per
respondent associated with the collection of clinical information.
Reporting forms for medical complications and medically ineligible
clients will be discontinued, the level of detail collected from
endoscopy and pathology reports will be reduced, and the reporting form
for colorectal cancer clinical data elements (CCDE) will be
streamlined. As a result, the reporting burden per CCDE form will be
similar regardless of primary test provided. Third, the collection of
patient-level reimbursement cost data will be discontinued and will be
replaced by the collection of program-level activity-based cost data
using a Cost Assessment Tool (CAT). 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.
Each program site will screen an estimated 375 patients per year.
De-identified CCDE information concerning approximately 187 new
screening records 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. Reporting is required
for all sites funded through the CRC screening program.
The goals of the expanded CRC screening program are to increase
population-based screening and to reduce health disparities in CRC
screening, incidence and mortality. The program will continue to
provide services to low-income individuals age 50 and older with
inadequate or no health insurance for CRC.
The total estimated annualized burden hours are 3,010. The increase
in the number of funded sites and the proposed changes will result in
an overall increase in burden to respondents. There are no costs to
respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
No. of No. of burden per
Type of respondents Form type respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Colorectal Cancer Screening Programs.. Clinical Data Elements.. 26 375 15/60
[[Page 17922]]
Cost Assessment Tool.... 26 1 22
----------------------------------------------------------------------------------------------------------------
Dated: March 31, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2010-7916 Filed 4-7-10; 8:45 am]
BILLING CODE 4163-18-P
