National Committee on Vital and Health Statistics: Meeting, 32338-32339 [05-10965]
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Federal Register / Vol. 70, No. 105 / Thursday, June 2, 2005 / Notices
This is a new data collection.
SUPPLEMENTARY INFORMATION:
Respondent type
Activity
Number of
respondents
Responses/
respondent
Time (hr)/
response
Total
burden
Program staff ...........
HIV/AIDS Knowledge Form (pre and post) .......
HIV/AIDS Risk Behavior Form ..........................
Encounter Form .................................................
Client Background Form ....................................
Process Evaluation Form-Staff ..........................
............................................................................
Client Utilization Form (RS/INR) ........................
6
6
14
6
18
....................
210
240
240
120
120
2
....................
1
0.25
0.33
0.25
0.17
1.00
....................
0.33
360
475
420
122
36
....................
70
Recruiting Script for Utilization survey ..............
............................................................................
´ ´
Protege Utilization Form ....................................
300
....................
8
1
....................
1
0.17
....................
0.50
51
....................
4
Organizational Assessment Questionnaire (pre
and post).
Process Evaluation Form-Director .....................
Stakeholder Survey ...........................................
12
2
1.50
36
18
24
2
1
1.00
1
36
24
$1,200.00
552
....................
....................
1,635
$1,200.00
Clients of Funded
programs.
Directors, Funded
programs.
Stakeholders ............
Total .................
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access the HHS Web
site address at https://www.hhs.gov/
oirm/infocollect/pending/ or e-mail your
request, including your address, phone
number, OMB number, and OS
document identifier, to
naomi.cook@hhs.gov, or call the Reports
Clearance Office on (202) 690–6162.
Written comments and
recommendations for the proposed
information collections must be mailed
within 30 days of this notice directly to
the Desk Officer at the address below:
OMB Desk Officer: John Kraemer, OMB
Human Resources and Housing Branch,
Attention: (OMB #0990–NEW), New
Executive Office Building, Room 10235,
Washington DC 20503.
Dated: May 20, 2005.
Robert E. Polson,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. 05–10980 Filed 6–1–05; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: OS–0990–0258]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Office of the Secretary.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Office of the Secretary (OS), Department
of Health and Human Services, is
AGENCY:
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publishing the following summary of
proposed collections for public
comment. Interested persons are invited
to send comments regarding this burden
estimate or any other aspect of this
collection of information, including any
of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
Type of Information Collection
Request: Extension of Currently
Approved Collection.
Title of Information Collection:
National Study of Stroke Post Acute
Care: Outcomes and Costs.
Form/OMB No.: OS–0990–0258.
Use: This study will provide
information on Medicare outcomes and
costs of care for Medicare beneficiaries
who suffer a stroke and received
treatment in a post acute care setting
skilled nursing facility, home health, or
rehabilitation hospital.
Frequency: Reporting on occasion.
Affected Public: Business or other forprofit, not-for-profit institutions; and
individuals or households.
Annual Number of Respondents: 350.
Total Annual Responses: 350.
Average Burden Per Response: 1 hour.
Total Annual Hours: 298.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access the HHS Web
site address at https://www.hhs.gov/
oirm/infocollect/pending/ or e-mail your
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Total cost to
respondent
$0.00
$0.00
request, including your address, phone
number, OMB number, and OS
document identifier, to
naomi.cook@hhs.gov, or call the Reports
Clearance Office on (202) 690–6162.
Written comments and
recommendations for the proposed
information collections must be mailed
within 60 days of this notice directly to
the OS Paperwork Clearance Officer
designated at the following address:
Department of Health and Human
Services, Office of the Secretary,
Assistant Secretary for Budget,
Technology, and Finance, Office of
Information and Resource Management,
Attention: Naomi Cook (0990–0258),
Room 531–H, 200 Independence
Avenue, SW., Washington, DC 20201.
Dated: May 20, 2005.
Robert E. Polson,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. 05–10981 Filed 6–1–05; 8:45 am]
BILLING CODE 4168–17–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Committee on Vital and Health
Statistics: Meeting
Pursuant to the Federal Advisory
Committee Act, the Department of
Health and Human Services (HHS)
announces the following advisory
committee meeting.
Name: National Committee on Vital and
Health Statistics (NCVHS).
Time and Date: June 29, 2005 9 a.m.–3:30
p.m., June 30, 2005 9 a.m.–3 p.m.
Place: Hubert H. Humphrey Building, 200
Independence Avenue, SW., Room 705A,
Washington, DC 20201.
Status: Open.
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Federal Register / Vol. 70, No. 105 / Thursday, June 2, 2005 / Notices
Purpose: At this meeting the Committee
will hear presentations and hold discussions
on several health data policy topics. On the
morning of the first day the Committee will
hear updates and status reports from the
Department on topics including Clinical Data
Standards, the Consolidated Health
Informatics Initiative, and HIPAA Privacy
Rule compliance. They will also discuss
drafts of two Committee reports. In the
afternoon the Committee will hear an update
from the Office of the National Coordinator
for Health Information Technology and
briefings on the Federal Health Architecture
initiative and the Commission on Systemic
Interoperability.
On the morning of the second day the
Committee will hear an update from the
Certification Commission for Healthcare
Information Technology (CCHIT) and a
presentation by an American National
Standards Institute’s Healthcare Informatics
Standards Board (ANSI HISB) panel. There
will also be an update on the National Health
Information Infrastructure and public health.
In the afternoon, there will be reports from
the subcommittees and a discussion of
agendas for future Committee meetings.
The times shown above are for the full
Committee meetings. Subcommittee breakout
sessions are scheduled for late in the
afternoon of the first day in the morning prior
to the full Committee meeting on the second
day. Agendas for these breakout sessions will
be posted on the NCVHS Web site (URL
below) when available.
Contact Person for More Information:
Substantive program information as well as
summaries of meetings and a roster of
committee members may be obtained from
Marjorie S. Greenberg, Executive Secretary,
NCVHS, National Center for Health statistics,
Centers for Disease Control and Prevention,
3311 Toledo Road, Room 2402, Hyattsville,
Maryland 20782, telephone (301) 458–4245.
Information also is available on the NCVHS
home page of the HHS Web site: https://
www.ncvhs.hhs.gov/, where further
information including an agenda will be
posted when available.
Should you require reasonable
accommodation, please contact the CDC
Office of Equal Employment Opportunity on
(301) 458–4EEO (4336) as soon as possible.
Dated: May 23, 2005.
James Scanlon,
Acting Deputy Assistant Secretary for Science
and Data Policy, Office of the Assistant
Secretary for Planning and Evaluation.
[FR Doc. 05–10965 Filed 6–1–05; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–05–05CJ)
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 404–371–5983 and
send comments to Seleda Perryman,
CDC Assistant 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
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
Colorectal Cancer Screening
Demonstration Program ‘‘New ’’
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
The CDC is requesting approval to
collect individual patient-level
screening, diagnostic, and treatment
data in association with a new
colorectal cancer screening
demonstration program. CDC is
planning to fund 3–5 cooperative
agreements in fiscal year (FY) 2005 to
implement new colorectal cancer (CRC)
demonstration programs. These 3-year
demonstration programs are designed to
increase population-based CRC
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32339
screening among persons 50 years and
older in a geographically defined area,
focusing screening efforts on persons
age 50 years and older with low
incomes and inadequate or no health
insurance coverage for CRC screening
(priority population).
Colorectal Cancer 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
with one or a combination of the
following tests: fecal occult blood
testing (FOBT), flexible sigmoidoscopy,
colonoscopy, and/or double-contrast
barium enema (DCBE). Fecal
immunochemical testing (FIT) is
considered an acceptable alternative to
FOBT. In the absence of evidence
indicating a single most effective test,
selected programs will be able to choose
which screening test(s) they will use
from the above list of recommended
tests.
All funded programs will be required
to submit patient-level data on CRC
screening and diagnostic services
provided as part of this demonstration
project, which will be used to assess the
quality and appropriateness of the
services delivered.
Programs that receive CDC funding to
provide screening and diagnostic
services will collect individual patientlevel data to capture demographic
information and clinical services and
outcomes, and submit these data to CDC
on a quarterly basis. Some of the
cooperative agreement recipients may
receive funding for program
components other than the provision of
screening and diagnostic services.
Programs that do not receive CDC
funding to provide screening and
diagnostic follow up services will still
collect individual patient-level data but
will only submit the data in aggregate to
CDC, on a quarterly basis. Grantees may
be asked by CDC to submit
individualized data if aggregate data do
not meet quality indicator standards.
While CDC funds will not be used for
treatment, programs will need to
monitor treatment and document that
patients are receiving appropriate
treatment services. Submitted data must
contain no patient identifiers.
All programs will additionally submit
annual program-level data to CDC to be
used to evaluate program effectiveness
and monitor cost, funding sources, and
an increase in population-based
screening over the 3-year program
period.
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]]>Agencies
[Federal Register Volume 70, Number 105 (Thursday, June 2, 2005)]
[Notices]
[Pages 32338-32339]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-10965]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Committee on Vital and Health Statistics: Meeting
Pursuant to the Federal Advisory Committee Act, the Department of
Health and Human Services (HHS) announces the following advisory
committee meeting.
Name: National Committee on Vital and Health Statistics (NCVHS).
Time and Date: June 29, 2005 9 a.m.-3:30 p.m., June 30, 2005 9
a.m.-3 p.m.
Place: Hubert H. Humphrey Building, 200 Independence Avenue,
SW., Room 705A, Washington, DC 20201.
Status: Open.
[[Page 32339]]
Purpose: At this meeting the Committee will hear presentations
and hold discussions on several health data policy topics. On the
morning of the first day the Committee will hear updates and status
reports from the Department on topics including Clinical Data
Standards, the Consolidated Health Informatics Initiative, and HIPAA
Privacy Rule compliance. They will also discuss drafts of two
Committee reports. In the afternoon the Committee will hear an
update from the Office of the National Coordinator for Health
Information Technology and briefings on the Federal Health
Architecture initiative and the Commission on Systemic
Interoperability.
On the morning of the second day the Committee will hear an
update from the Certification Commission for Healthcare Information
Technology (CCHIT) and a presentation by an American National
Standards Institute's Healthcare Informatics Standards Board (ANSI
HISB) panel. There will also be an update on the National Health
Information Infrastructure and public health. In the afternoon,
there will be reports from the subcommittees and a discussion of
agendas for future Committee meetings.
The times shown above are for the full Committee meetings.
Subcommittee breakout sessions are scheduled for late in the
afternoon of the first day in the morning prior to the full
Committee meeting on the second day. Agendas for these breakout
sessions will be posted on the NCVHS Web site (URL below) when
available.
Contact Person for More Information: Substantive program
information as well as summaries of meetings and a roster of
committee members may be obtained from Marjorie S. Greenberg,
Executive Secretary, NCVHS, National Center for Health statistics,
Centers for Disease Control and Prevention, 3311 Toledo Road, Room
2402, Hyattsville, Maryland 20782, telephone (301) 458-4245.
Information also is available on the NCVHS home page of the HHS Web
site: https://www.ncvhs.hhs.gov/, where further information including
an agenda will be posted when available.
Should you require reasonable accommodation, please contact the
CDC Office of Equal Employment Opportunity on (301) 458-4EEO (4336)
as soon as possible.
Dated: May 23, 2005.
James Scanlon,
Acting Deputy Assistant Secretary for Science and Data Policy, Office
of the Assistant Secretary for Planning and Evaluation.
[FR Doc. 05-10965 Filed 6-1-05; 8:45 am]
BILLING CODE 4151-05-M
