Proposed Data Collections Submitted for Public Comment and Recommendations, 64652-64653 [E7-22421]
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64652
Federal Register / Vol. 72, No. 221 / Friday, November 16, 2007 / Notices
ESTIMATED ANNUALIZED BURDEN—Continued
Average
burden per
respondent
(in hours)
Instrument name
Principal ..............
Baseline implementation survey ................................................................
Mid-implementation survey ........................................................................
End-of-school-year implementation survey ................................................
Baseline implementation survey ................................................................
49
32
49
49
1
1
1
1
15/60
15/60
15/60
15/60
Mid-implementation survey ........................................................................
End-of-school-year implementation survey ................................................
Follow-up implementation survey ..............................................................
Baseline implementation survey ................................................................
Cost survey ................................................................................................
Fifth session mid-implementation survey ...................................................
Ninth session mid-implementation survey .................................................
32
49
49
98
49
98
98
1
1
1
1
11
2
2
15/60
15/60
5/60
15/60
20/60
25/60
25/60
Prevention coordinator.
Teacher ...............
Dated: November 9, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Office of
the Chief Science Officer.
[FR Doc. E7–22419 Filed 11–15–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Proposed Data Collections Submitted
for Public Comment and
Recommendations
mstockstill on PROD1PC66 with NOTICES
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
whether the information shall have
practical utility; (b) the accuracy of the
21:48 Nov 15, 2007
Jkt 214001
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
[60Day–08–08AC]
VerDate Aug<31>2005
Number of
respondents
Number of responses per
respondent
Type of respondent
Racial and Ethnic Approaches to
Community Health (REACH) U.S.
Evaluation—New—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
REACH U.S. is an effort to meet the
Healthy People 2010 goal of eliminating
health disparities in the health status of
racial and ethnic minorities. After initial
review of the national data, a study
approach was adopted on the statistical
techniques of ‘‘excess deaths’’ to define
the difference in minority health in
relation to non-minority health. The
analysis of excess deaths revealed that
several specific health areas accounted
for the majority of the higher annual
proportion of minority deaths. Because
of these sobering statistics, and the
overarching goals of Healthy People
2010, REACH U.S. is being launched as
a national multi-level community
intervention program that serves
communities with African American,
PO 00000
Frm 00079
Fmt 4703
Sfmt 4703
American Indian, Hispanic American,
Asian American, and Pacific Islander
citizens. The REACH U.S. program
supports community coalitions in
designing, implementing, and
evaluating community-driven strategies
to eliminate health disparities in several
priority areas: Cardiovascular diseases,
diabetes, asthma, infant mortality, breast
and cervical cancer screening and
management, and adult immunization.
As part of the evaluation of the
REACH U.S. initiative, CDC proposes to
conduct risk factor surveys by
computer-assisted telephone interview
(CATI) in 29 communities participating
in REACH U.S. activities. Surveys will
be available in English, Spanish,
Vietnamese, Khmer, and Mandarin
Chinese. The target number of surveys
for each community is 900 adults, aged
18 and older, who belong to the racial/
ethnic group served by the communitybased program intervention. In
communities that focus on breast and
cervical cancer interventions,
approximately 250 of the 900 interviews
will involve women aged 40–64 years.
Respondents will be identified through
list-assisted random-digit dialing
methods. The surveys will help to
assess the prevalence of various risk
factors associated with chronic diseases,
deficits in breast and cervical cancer
screening and management, and deficits
in adult immunizations. The surveys
will also assess progress towards the
national goal of eliminating health
disparities within the communities.
There are no costs to respondents
other than their time.
E:\FR\FM\16NON1.SGM
16NON1
64653
Federal Register / Vol. 72, No. 221 / Friday, November 16, 2007 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Members of REACH U.S.
Communities.
No. of respondents
Form name
Screening Interview ..............
...............................................
2/60
3,340
26,100
1
15/60
6,525
..............................
..............................
..............................
9,865
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4163–18–P
[Document Identifier: CMS–10230]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Proposed Data Collections Submitted
for Public Comment and
Recommendations; Correction Centers
for Disease Control and Prevention;
Notice; Correction
The Centers for Disease Control and
Prevention published a document in the
Federal Register concerning a retraction
of a previously published 60-day
Federal Register Notice. The document
contained the incorrect Federal Register
Notice number.
FOR FURTHER INFORMATION CONTACT:
Maryam Daneshvar, 404–639–4604.
Correction
In the Federal Register of November
7, 2007, Volume 72, Number 215, in FR
Doc. E7–21864 page 62857, under the
agency name correct the Federal
Register notice number 60 Day–07–
07BS to read: 60 Day–07–06BS.
Dated: November 7, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–22420 Filed 11–15–07; 8:45 am]
mstockstill on PROD1PC66 with NOTICES
BILLING CODE 4163–18–P
VerDate Aug<31>2005
21:48 Nov 15, 2007
Jkt 214001
Centers for Medicare & Medicaid
Services
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS) is 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.
1. Type of Information Collection
Request: New collection; Title of
Information Collection: PACE Audit
Guide Version 1; Use: CMS conducts a
comprehensive annual on-site review of
Programs of All-Inclusive Care for the
Elderly (PACE) program provider
operations in order to assure contract
compliance during the first three years
(the trail period) with CMS and the
State administering agency. Onsite
monitoring continues at least every 2
years after the first 3-year trial period
ends. The purpose of the guide is
oversight, monitoring, compliance and
auditing of the activities necessary to
ensure quality provision of the Medicare
Parts A, B and D benefits to
beneficiaries. Form Number: CMS–
10230 (OMB#: 0938–New); Frequency:
AGENCY:
[60 Day–07–07BS]
PO 00000
Frm 00080
Total burden
(in hrs)
1
Dated: November 9, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–22421 Filed 11–15–07; 8:45 am]
Centers for Disease Control and
Prevention
Avg. burden per
response
(in hrs)
100,200
REACH U.S. Risk Factor
Survey.
Total ...............................
No. of responses
per respondent
Fmt 4703
Sfmt 4703
Yearly; Affected Public: Private sector—
Business or other for-profit and Not-forprofit institutions; Number of
Respondents: 22; Total Annual
Responses: 22; Total Annual Hours:
6,336.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web Site
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786–
1326.
To be assured consideration,
comments and recommendations for the
proposed information collections must
be received at the address below, no
later than 5 p.m. on January 15, 2008.
CMS, Office of Strategic Operations and
Regulatory Affairs, Division of
Regulations Development–C, Attention:
Bonnie L Harkless, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
Dated: November 8, 2007.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E7–22255 Filed 11–15–07; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–382]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS), Department of Health
AGENCY:
E:\FR\FM\16NON1.SGM
16NON1
]]>Agencies
[Federal Register Volume 72, Number 221 (Friday, November 16, 2007)]
[Notices]
[Pages 64652-64653]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-22421]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-08-08AC]
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 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
Racial and Ethnic Approaches to Community Health (REACH) U.S.
Evaluation--New--National Center for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
REACH U.S. is an effort to meet the Healthy People 2010 goal of
eliminating health disparities in the health status of racial and
ethnic minorities. After initial review of the national data, a study
approach was adopted on the statistical techniques of ``excess deaths''
to define the difference in minority health in relation to non-minority
health. The analysis of excess deaths revealed that several specific
health areas accounted for the majority of the higher annual proportion
of minority deaths. Because of these sobering statistics, and the
overarching goals of Healthy People 2010, REACH U.S. is being launched
as a national multi-level community intervention program that serves
communities with African American, American Indian, Hispanic American,
Asian American, and Pacific Islander citizens. The REACH U.S. program
supports community coalitions in designing, implementing, and
evaluating community-driven strategies to eliminate health disparities
in several priority areas: Cardiovascular diseases, diabetes, asthma,
infant mortality, breast and cervical cancer screening and management,
and adult immunization.
As part of the evaluation of the REACH U.S. initiative, CDC
proposes to conduct risk factor surveys by computer-assisted telephone
interview (CATI) in 29 communities participating in REACH U.S.
activities. Surveys will be available in English, Spanish, Vietnamese,
Khmer, and Mandarin Chinese. The target number of surveys for each
community is 900 adults, aged 18 and older, who belong to the racial/
ethnic group served by the community-based program intervention. In
communities that focus on breast and cervical cancer interventions,
approximately 250 of the 900 interviews will involve women aged 40-64
years. Respondents will be identified through list-assisted random-
digit dialing methods. The surveys will help to assess the prevalence
of various risk factors associated with chronic diseases, deficits in
breast and cervical cancer screening and management, and deficits in
adult immunizations. The surveys will also assess progress towards the
national goal of eliminating health disparities within the communities.
There are no costs to respondents other than their time.
[[Page 64653]]
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
No. of No. of responses Avg. burden per Total burden (in
Type of respondents Form name respondents per respondent response (in hrs) hrs)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Members of REACH U.S. Communities........... Screening Interview........... 100,200 1 2/60 3,340
REACH U.S. Risk Factor Survey. 26,100 1 15/60 6,525
---------------------------------------------------------------------------
Total................................... .............................. ................. ................. ................. 9,865
--------------------------------------------------------------------------------------------------------------------------------------------------------
Dated: November 9, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E7-22421 Filed 11-15-07; 8:45 am]
BILLING CODE 4163-18-P
