Proposed Data Collections Submitted for Public Comment and Recommendations, 76469-76470 [2010-30764]
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Federal Register / Vol. 75, No. 235 / Wednesday, December 8, 2010 / Notices
more accurately measure health
spending. Although panelists are not
limited in the topics they may discuss,
the Panel is not expected to discuss or
recommend changes in current or future
Medicare provider payment rates or
coverage policy.
Meeting Dates: December 13, 2010,
9:30 a.m. to 5 p.m. and December 14,
2010, 8:30 a.m.–1 p.m. e.t.
ADDRESSES: The meeting will be held at
HHS Centers for Medicare and Medicaid
Services headquarters located at 7500
Security Blvd., Baltimore, Maryland
21244, Conference Room B.
Comments: The meeting will allocate
time on the agenda to hear public
comments. In lieu of oral comments,
formal written comments may be
submitted for the record to Donald T.
Oellerich, OASPE, 200 Independence
Ave., SW., 20201, Room 405F. Those
submitting written comments should
identify themselves and any relevant
organizational affiliations.
FOR FURTHER INFORMATION CONTACT:
Donald T. Oellerich (202) 690–8410,
Don.oellerich@hhs.gov. Note: Although
the meeting is open to the public,
procedures governing security
procedures and the entrance to Federal
buildings may change without notice.
Those wishing to attend the meeting
must call or e-mail Dr. Oellerich by
Thursday, December 9, 2010, so that
their name may be put on a list of
expected attendees and forwarded to the
security officers at HHS Headquarters.
SUPPLEMENTARY INFORMATION: Topics of
the Meeting: The Panel is specifically
charged with discussing and possibly
making recommendations to the
Medicare Trustees on how the Trustees
might more accurately estimate the long
term rate of health spending in the
United States. The discussion is
expected to focus on highly technical
aspects of estimation involving
economics and actuarial science.
Panelists are not restricted, however, in
the topics that they choose to discuss.
Procedure and Agenda: This meeting
is open to the public. The Panel will
likely hear presentations from Medicare
public trustees on issues they wish the
panel to address. This may be followed
by HHS staff presentations regarding
long range growth. After any
presentations, the Panel will deliberate
openly on the topic. Interested persons
may observe the deliberations, but the
Panel will not hear public comments
during this time. The Panel will also
allow an open public session for any
attendee to address issues specific to the
topic.
Authority: 42 U.S.C. 217a; Section 222 of
the Public Health Services Act, as amended.
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18:23 Dec 07, 2010
Jkt 223001
The panel is governed by provisions of
Public Law 92–463, as amended (5 U.S.C.
Appendix 2), which sets forth standards for
the formation and use of advisory
committees.
Dated: December 2, 2010.
Sherry Glied,
Assistant Secretary for Planning and
Evaluation.
[FR Doc. 2010–30838 Filed 12–7–10; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–11–0679]
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 or send
comments to Carol E. Walker, CDC
Acting Reports Clearance Officer, 1600
Clifton Road, MS D–74, 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
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
Division of Heart Disease and Stroke
Prevention Management Information
System—Revision—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
PO 00000
Frm 00077
Fmt 4703
Sfmt 4703
76469
Background and Brief Description
CDC’s Division of Heart Disease and
Stroke Prevention (DHDSP) is currently
approved to collect progress and activity
information from awardees funded
through two programs: The National
Heart Disease and Stroke Prevention
Program (NHDSPP), and the WellIntegrated Screening and Evaluation for
Women Across the Nation
(WISEWOMAN) program. Information is
collected semi-annually through an
electronic Management Information
System (MIS). The current approval is
scheduled to expire 5/31/2011 (OMB
No. 0920–0679).
CDC plans to request OMB approval
to continue information collection, with
changes, for three years. A net reduction
in the number of respondents will result
in a net reduction in burden hours.
Although there will be an increase in
the number of state-based heart disease
and stroke prevention (HDSP) programs
funded through the NHDSPP, reporting
requirements involving the MIS will be
discontinued for awardees funded
through the WISEWOMAN program. No
changes are proposed to the information
collection instrument, the burden per
response, or the frequency of
information collection.
In 1998, Congress provided CDC with
initial funding to establish the NHDSPP,
authorized under sections 301(a) and
317b(k)(2) of the Public Health Service
(PHS) Act [42 U.S.C. 241(a) and
247b(k)(2)], as amended. The program
currently supports population-based
heart disease and stroke prevention
efforts in selected States and the District
of Columbia. As funding allows, CDC’s
strategic plan calls for expanding the
program to health departments in all
U.S. States and territories. CDC works
with HDSP program awardees to
implement and evaluate evidence-based
public health prevention and control
strategies that address risk factors and
reduce disparities, disease, disability,
and death from heart disease and stroke.
Awardees are encouraged to work at the
highest levels within priority
environments to change policies and
systems that will improve
cardiovascular outcomes.
All HDSP program awardees are
required to submit continuation
applications and semi-annual progress
reports to CDC. The DHDSP MIS
provides a standardized, electronic
interface for the collection of this
progress information, which includes
work plans, objectives, partners, data
sources, and policy and environmental
assessments. The MIS also produces
both state-specific and aggregate reports
that are used for performance
E:\FR\FM\08DEN1.SGM
08DEN1
76470
Federal Register / Vol. 75, No. 235 / Wednesday, December 8, 2010 / Notices
monitoring, program evaluation, and
technical assistance. The monitoring
and evaluation plan for the HDSP
program is part of an overall initiative
within CDC’s National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP) to promote more
efficient ways of using resources and
achieving greater health impact. CDC
plans to increase the number of HDSP
awardees reporting through the MIS
from 33 to 42.
CDC will discontinue approval to use
the DHDSP MIS for collecting
information from WISEWOMAN
program awardees. The WISEWOMAN
program is a demonstration program
that extends cardiovascular diseaserelated services to a subset of women
who also receive services through the
National Breast and Cervical Cancer
Early Detection Program (NBCCEDP).
Although approval was obtained to use
the DHDSP MIS for collecting progress
and activity information from
WISEWOMAN awardees, the
information collection was not
implemented due to a change in plans
for monitoring these awardees. The
current WISEWOMAN data collection is
described in OMB No. 0920–0612
(WISEWOMAN Reporting System, exp.
3/31/2013).
CDC will continue to use the
information collected through the
DHDSP MIS to identify state-specific
heart disease and stroke prevention
priorities and objectives, and to describe
the impact and reach of program
interventions. Respondents will be 42
health departments in 41 States and the
District of Columbia (DC). Respondents
will continue to submit their progress
and activity information to CDC semiannually. The estimated burden per
response is six hours. There are no costs
to respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Respondents
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
State-Based HDSP Programs .........................................................................
42
2
6
504
Dated: December 2, 2010.
Carol Walker,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2010–30764 Filed 12–7–10; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Proposed Project
[60 Day–11–0770]
jlentini on DSKJ8SOYB1PROD with NOTICES
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 or send
comments to Carol Walker, Acting CDC
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
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
VerDate Mar<15>2010
18:23 Dec 07, 2010
Jkt 223001
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.
National HIV Behavioral Surveillance
System (NHBS) (OMB no. 0920–0770,
exp. 03/31/2011)—Extension—National
Center for HIV, Hepatitis, STD, and TB
Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The purpose of this data collection is
to monitor behaviors related to Human
Immunodeficiency Virus (HIV) infection
among persons at high risk for infection
in the United States. The primary
objectives of the NHBS system are to
obtain data from samples of persons at
risk to: (a) Describe the prevalence and
trends in risk behaviors; (b) describe the
prevalence of and trends in HIV testing
and HIV infection; (c) describe the
prevalence of and trends in use of HIV
prevention services; (d) identify met and
unmet needs for HIV prevention
services in order to inform health
departments, community based
organizations, community planning
groups and other stakeholders.
This project addresses the goals of the
National HIV/AIDS Strategy for the
United States, which calls for State and
PO 00000
Frm 00078
Fmt 4703
Sfmt 4703
local health departments to monitor
progress towards the national goal of
reducing new HIV infections by 25% by
2015. NHBS contributes to this national
goal by describing and monitoring the
HIV risk behaviors, HIV seroprevalence
and incidence, and HIV prevention
experiences of persons at highest risk
for HIV infection.
The Centers for Disease Control and
Prevention request approval for a 3-year
extension for the previously approved
National HIV Behavioral Surveillance
System (NHBS), OMB number 0920–
0770, which expires 03/31/2011. Data
are collected through anonymous, inperson interviews conducted with
persons systematically selected from 25
Metropolitan Statistical Areas (MSAs)
throughout the United States; these 25
MSAs were chosen based on having
high AIDS prevalence. Persons at risk
for HIV infection to be interviewed for
NHBS include men who have sex with
men (MSM), injecting drug users (IDU),
and heterosexuals at increased risk of
HIV (HET). A brief screening interview
will be used to determine eligibility for
participation in the behavioral
assessment.
The data from the behavioral
assessment will provide frequency
estimates of behavior related to the risk
of HIV and other sexually transmitted
diseases, prior testing for HIV, and use
of HIV prevention services. All persons
interviewed will also be offered an HIV
test, and will participate in a pre-test
counseling session. No other Federal
agency systematically collects this type
of information from persons at risk for
HIV infection. These data will have a
E:\FR\FM\08DEN1.SGM
08DEN1
Agencies
[Federal Register Volume 75, Number 235 (Wednesday, December 8, 2010)]
[Notices]
[Pages 76469-76470]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-30764]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-11-0679]
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 or
send comments to Carol E. Walker, CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS D-74, 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 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
Division of Heart Disease and Stroke Prevention Management
Information System--Revision--National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
CDC's Division of Heart Disease and Stroke Prevention (DHDSP) is
currently approved to collect progress and activity information from
awardees funded through two programs: The National Heart Disease and
Stroke Prevention Program (NHDSPP), and the Well-Integrated Screening
and Evaluation for Women Across the Nation (WISEWOMAN) program.
Information is collected semi-annually through an electronic Management
Information System (MIS). The current approval is scheduled to expire
5/31/2011 (OMB No. 0920-0679).
CDC plans to request OMB approval to continue information
collection, with changes, for three years. A net reduction in the
number of respondents will result in a net reduction in burden hours.
Although there will be an increase in the number of state-based heart
disease and stroke prevention (HDSP) programs funded through the
NHDSPP, reporting requirements involving the MIS will be discontinued
for awardees funded through the WISEWOMAN program. No changes are
proposed to the information collection instrument, the burden per
response, or the frequency of information collection.
In 1998, Congress provided CDC with initial funding to establish
the NHDSPP, authorized under sections 301(a) and 317b(k)(2) of the
Public Health Service (PHS) Act [42 U.S.C. 241(a) and 247b(k)(2)], as
amended. The program currently supports population-based heart disease
and stroke prevention efforts in selected States and the District of
Columbia. As funding allows, CDC's strategic plan calls for expanding
the program to health departments in all U.S. States and territories.
CDC works with HDSP program awardees to implement and evaluate
evidence-based public health prevention and control strategies that
address risk factors and reduce disparities, disease, disability, and
death from heart disease and stroke. Awardees are encouraged to work at
the highest levels within priority environments to change policies and
systems that will improve cardiovascular outcomes.
All HDSP program awardees are required to submit continuation
applications and semi-annual progress reports to CDC. The DHDSP MIS
provides a standardized, electronic interface for the collection of
this progress information, which includes work plans, objectives,
partners, data sources, and policy and environmental assessments. The
MIS also produces both state-specific and aggregate reports that are
used for performance
[[Page 76470]]
monitoring, program evaluation, and technical assistance. The
monitoring and evaluation plan for the HDSP program is part of an
overall initiative within CDC's National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP) to promote more efficient
ways of using resources and achieving greater health impact. CDC plans
to increase the number of HDSP awardees reporting through the MIS from
33 to 42.
CDC will discontinue approval to use the DHDSP MIS for collecting
information from WISEWOMAN program awardees. The WISEWOMAN program is a
demonstration program that extends cardiovascular disease-related
services to a subset of women who also receive services through the
National Breast and Cervical Cancer Early Detection Program (NBCCEDP).
Although approval was obtained to use the DHDSP MIS for collecting
progress and activity information from WISEWOMAN awardees, the
information collection was not implemented due to a change in plans for
monitoring these awardees. The current WISEWOMAN data collection is
described in OMB No. 0920-0612 (WISEWOMAN Reporting System, exp. 3/31/
2013).
CDC will continue to use the information collected through the
DHDSP MIS to identify state-specific heart disease and stroke
prevention priorities and objectives, and to describe the impact and
reach of program interventions. Respondents will be 42 health
departments in 41 States and the District of Columbia (DC). Respondents
will continue to submit their progress and activity information to CDC
semi-annually. The estimated burden per response is six hours. There
are no costs to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Respondents Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
State-Based HDSP Programs................... 42 2 6 504
----------------------------------------------------------------------------------------------------------------
Dated: December 2, 2010.
Carol Walker,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2010-30764 Filed 12-7-10; 8:45 am]
BILLING CODE 4163-18-P