Attachment 2 - Federal Register Notice - 60-Day

Attachment 2. 60-day FRN.pdf

Racial and Ethnic Approaches to Community Health across the U.S. (REACH U.S.) Evaluation

Attachment 2 - Federal Register Notice - 60-Day

OMB: 0920-0805

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64652

Federal Register / Vol. 72, No. 221 / Friday, November 16, 2007 / Notices
ESTIMATED ANNUALIZED BURDEN—Continued

Principal ..............

Baseline implementation survey ................................................................
Mid-implementation survey ........................................................................
End-of-school-year implementation survey ................................................
Baseline implementation survey ................................................................

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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 .................................................

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49
98
98

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2
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15/60
15/60
5/60
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20/60
25/60
25/60

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
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
[email protected].
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

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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]

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Average
burden per
respondent
(in hours)

Instrument name

Prevention coordinator.

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,

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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.

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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 ..............

...............................................

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]

2/60

3,340

26,100

1

15/60

6,525

..............................

..............................

..............................

9,865

[60 Day–07–07BS]

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]

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21:48 Nov 15, 2007

Centers for Medicare & Medicaid
Services

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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:

Centers for Disease Control and
Prevention

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DEPARTMENT OF HEALTH AND
HUMAN SERVICES

Agency Information Collection
Activities: Proposed Collection;
Comment Request

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

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Total burden
(in hrs)

1

[Document Identifier: CMS–10230]

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Avg. burden per
response
(in hrs)

100,200

REACH U.S. Risk Factor
Survey.
Total ...............................

No. of responses
per respondent

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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 http://www.cms.hhs.gov/
PaperworkReductionActof1995, or email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
[email protected], 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]
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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:

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File Typeapplication/pdf
File TitleDocument
SubjectExtracted Pages
AuthorU.S. Government Printing Office
File Modified2008-01-02
File Created2007-11-16

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