Att 2a - Pubd 60d FRN

Att 2a - Pubd 60d FRN.pdf

Monitoring and Reporting System for DELTA FOCUS Awardees

Att 2a - Pubd 60d FRN

OMB: 0920-0968

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49798

Federal Register / Vol. 77, No. 160 / Friday, August 17, 2012 / Notices

and in-depth interview participants
(total 1000) will complete a brief paper

and pencil survey. The total estimated
annual burden hours are 2311.

There are no costs to the respondents
other than their time.

ESTIMATED ANNUALIZED BURDEN HOURS
Respondents

Individuals
Individuals
Individuals
Individuals
Individuals

(males
(males
(males
(males
(males

and
and
and
and
and

females)
females)
females)
females)
females)

aged
aged
aged
aged
aged

18–64
18–64
18–64
18–64
18–64

Kimberly S. Lane,
Deputy Director, Office of Science Integrity,
Office of the Associate Director for Science,
Office of the Director, Centers for Disease
Control and Prevention.

Proposed Project
Monitoring And Reporting System For
DELTA FOCUS Awardees—New—
National Center for Injury Prevention
and Control (NCIPC), Centers for
Disease Control and Prevention (CDC).

BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–12–12QR]

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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 404–639–7570 and
send comments to Kimberly S. Lane,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an email 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
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

15:13 Aug 16, 2012

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Study screener ...............................................
In-Depth Interview Guide ...............................
Focus Group Guide ........................................
Paper and Pencil Survey ...............................
Intercept Interview Guide ...............................

be received within 60 days of this
notice.

[FR Doc. 2012–20213 Filed 8–16–12; 8:45 am]

VerDate Mar<15>2010

Number of
respondents

Form name

Background and Brief Description
Intimate Partner Violence (IPV) is a
serious, preventable public health
problem that affects millions of
Americans and results in serious
consequences for victims, families, and
communities. IPV occurs between two
people in a close relationship. The term
‘‘intimate partner’’ describes physical,
sexual, or psychological harm by a
current or former partner or spouse. IPV
can impact health in many ways,
including long-term health problems,
emotional impacts, and links to negative
health behaviors. IPV exists along a
continuum from a single episode of
violence to ongoing battering; many
victims do not report IPV to police,
friends, or family.
Research indicates that on average, 24
people per minute are victims of rape,
physical violence, or stalking by an
intimate partner in the United States.
Over the course of one year, more than
12 million women and men reported
being a victim of rape, physical
violence, or stalking by an intimate
partner. Also, on average nearly three
women are murdered each day by an
intimate partner. In 2007, IPV resulted
in more than 2,300 deaths. Of these
deaths, 30 percent were men and 70
percent were women. The medical care,
mental health services, and lost
productivity (e.g., time away from work)
cost of IPV is estimated at $8.3 billion
per year.
The objective of primary prevention is
to stop IPV before it occurs. In 2002,
authorized by the Family Violence
Prevention Services Act (FVPSA), CDC
developed the Domestic Violence
Prevention Enhancements and

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2338
500
500
1000
700

Number of
responses per
respondent
1
1
1
1
1

Average
burden per
response
(in hours)
2/60
1
2
30/60
20/60

Leadership Through Alliances (DELTA)
Program, with a focus on the primary
prevention of IPV. The CDC funded
DELTA Program provides funding to
state domestic violence coalitions
(SDVCs) to engage in statewide primary
prevention efforts and to provide
training, technical assistance, and
financial support to local communities
for local primary prevention efforts.
DELTA FOCUS (Domestic Violence
Prevention Enhancement and
Leadership Through Alliances, Focusing
on Outcomes for Communities United
with States) builds on that history by
providing focused funding to states and
communities for intensive
implementation and evaluation of IPV
primary prevention strategies that
address the structural determinants of
health at the societal and community
levels of the social-ecological model
(SEM).
By emphasizing primary prevention,
the DELTA FOCUS program will
support comprehensive and coordinated
approaches to IPV prevention. The
strategies will address the structural
determinants of health at the outer
layers (societal and community) of the
SEM that coordinate and align with
existing prevention strategies at the
inner layers of the SEM. This program
addresses the ‘‘Healthy People 2020’’
focus area(s) of Injury and Violence
Prevention and Social Determinants of
Health.
Information will be collected from the
12 DELTA FOCUS awardees through an
electronic Performance Management
Information System (PMIS). The PMIS
will collect information about the
staffing resources dedicated by each
awardee, as well as partnerships with
external organizations. Information
collected through the PMIS will be used
to inform performance monitoring and
program evaluation. Information will
also be used to respond to requests from
the National Center for Injury
Prevention and Control, Department of
Health and Human Services, White
House, Congress, and other sources.

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Federal Register / Vol. 77, No. 160 / Friday, August 17, 2012 / Notices
DELTA FOCUS awardees will use the
information collection to manage and
coordinate their activities and to
improve their efforts to prevent IPV.
The PMIS will collect a limited
amount of information in identifiable
form (IIF) for key program staff (e.g.,
Executive Director). Only names and
professional contact information will be

collected, limiting the potential negative
impact this data collection might have
on the privacy of respondents. No
personal contact information will be
collected. All respondents will be state
and territorial domestic violence
coalitions. The time commitments for
data entry and training are greatest

during the initial population of the
PMIS, typically in the first six months
of funding. Estimated burden for the
first-time population of the PMIS is
fifteen hours. Semi-Annual Reporting is
estimated at three hours per respondent.
There are no costs to respondents
other than their time.

ESTIMATED ANNUALIZED BURDEN TO RESPONDENTS
Number of
respondents

Type of respondents

Form name

State and/or Territorial Domestic Violence Coalitions.

DELTA FOCUS PMIS: Initial population.
DELTA FOCUS PMIS: Semi-annual
reporting.

Total ...........................................

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

Average
burden per
response
in hours)

Total burden
(in hours)

12

1

15

180

12

2

3

72

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

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

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

252

Kimberly S. Lane,
Deputy Director, Office of Scientific Integrity,
Office of the Associate Director for Science,
Office of the Director, Centers for Disease
Control and Prevention.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

[FR Doc. 2012–20211 Filed 8–16–12; 8:45 am]

[CMS–9074–N]

and interpretive regulations, and other
Federal Register notices that were
published from April through June
2012, relating to the Medicare and
Medicaid programs and other programs
administered by CMS.

Centers for Medicare & Medicaid
Services

BILLING CODE 4163–18–P

Medicare and Medicaid Programs;
Quarterly Listing of Program
Issuances—April Through June 2012
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:

This quarterly notice lists
CMS manual instructions, substantive

SUMMARY:

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Number of
responses per
respondent

It is
possible that an interested party may
need specific information and not be
able to determine from the listed
information whether the issuance or
regulation would fulfill that need.
Consequently, we are providing contact
persons to answer general questions
concerning each of the addenda
published in this notice.

FOR FURTHER INFORMATION CONTACT:

Addenda

Contact

I CMS Manual Instructions ......................................................
II Regulation Documents Published in the Federal Register
III CMS Rulings .......................................................................
IV Medicare National Coverage Determinations .....................
V FDA-Approved Category B IDEs .........................................
VI Collections of Information ...................................................
VII Medicare-Approved Carotid Stent Facilities ......................
VIII American College of Cardiology-National Cardiovascular
Data Registry Sites.
IX Medicare’s Active Coverage-Related Guidance Documents.
X One-time Notices Regarding National Coverage Provisions
XI National Oncologic Positron Emission Tomography Registry Sites.
XII Medicare-Approved Ventricular Assist Device (Destination Therapy) Facilities.
XIII Medicare-Approved Lung Volume Reduction Surgery Facilities.
XIV Medicare-Approved Bariatric Surgery Facilities ...............
XV Fluorodeoxyglucose Positron Emission Tomography for
Dementia Trials.
All Other Information ..................................................................

Ismael Torres ...........................................................................
Terri Plumb ...............................................................................
Tiffany Lafferty .........................................................................
Wanda Belle .............................................................................
John Manlove ...........................................................................
Mitch Bryman ...........................................................................
Sarah J. McClain ......................................................................
JoAnna Baldwin, MS ................................................................

(410)
(410)
(410)
(410)
(410)
(410)
(410)
(410)

Lori Ashby ................................................................................

(410) 786–6322

Lori Ashby ................................................................................
Stuart Caplan, RN, MAS ..........................................................

(410) 786–6322
(410) 786–8564

JoAnna Baldwin, MS ................................................................

(410) 786–7205

JoAnna Baldwin, MS ................................................................

(410) 786–7205

Kate Tillman, RN, MAS ............................................................
Stuart Caplan, RN, MAS ..........................................................

(410) 786–9252
(410) 786–8564

Annette Brewer ........................................................................

(410) 786–6580

I. Background
Among other things, the Centers for
Medicare & Medicaid Services (CMS) is

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responsible for administering the
Medicare and Medicaid programs and
coordination and oversight of private

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Phone No.
786–1864
786–4481
786–7548
786–7491
786–6877
786–5258
786–2294
786–7205

health insurance. Administration and
oversight of these programs involves the
following: (1) Furnishing information to

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