Att B - 60 day FRN

Federal Register / Vol. 77, No. 68 / Monday, April 9, 2012 / Notices
(12 CFR 225.28) or that the Board has
determined by Order to be closely
related to banking and permissible for
bank holding companies. Unless
otherwise noted, these activities will be
conducted throughout the United States.
Each notice is available for inspection
at the Federal Reserve Bank indicated.
The notice also will be available for
inspection at the offices of the Board of
Governors. Interested persons may
express their views in writing on the
question whether the proposal complies
with the standards of section 4 of the
BHC Act.
Unless otherwise noted, comments
regarding the applications must be
received at the Reserve Bank indicated
or the offices of the Board of Governors
not later than April 24, 2012.
A. Federal Reserve Bank of Richmond
(Adam M. Drimer, Assistant Vice
President) 701 East Byrd Street,
Richmond, Virginia 23261–4528:
1. City Holding Company, Cross
Lanes, West Virginia; to acquire 100
percent of the voting shares of Virginia
Savings Bancorp, Inc., and thereby
indirectly acquire Virginia Savings
Bank, F.S.B., both in Front Royal,
Virginia, and thereby engage in
operating a savings and loan
association, pursuant to section
225.28(4)(ii).
Board of Governors of the Federal Reserve
System, April 4, 2012.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. 2012–8480 Filed 4–6–12; 8:45 am]
BILLING CODE 6210–01–P

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

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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 or send
comments to Ron Otten, at CDC, 1600
Clifton Road, MS D–74, Atlanta, GA
30333 or send an email to omb@cdc.gov.

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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
Evaluation of U.S. Family Planning
Guidelines—New—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention’s (CDC) Division of
Reproductive Health (DRH), in
collaboration with the Office of
Population Affairs (OPA), plans to
conduct an evaluation of the diffusion,
utilization of, and impact on providerand clinic-level attitudes and practices
of three national guidance documents.
These guidelines, which are intended to
improve contraceptive use and the
delivery of quality family planning
services in the United States, are: (1)
The U.S. Medical Eligibility Criteria for
Contraceptive Use (U.S. MEC); (2) the
forthcoming U.S. Selected Practice
Recommendations for Contraceptive
Use (U.S. SPR); and (3) the forthcoming
Guidelines for Providing Quality Family
Planning Services (QFPS). The guidance
documents have or will be widely
disseminated to health-care providers
and other constituents, via professional
organizations, federal program grantees,
scientific and programmatic meetings,
scientific manuscripts, online resources,
and other avenues, as deemed
appropriate. The purpose of this
information collection is to evaluate the
adoption and implementation of
recommendations included in the U.S.
MEC, approximately two years after its
release, and to collect baseline
information on selected attitudes and
practices that will be addressed in the
forthcoming U.S. SPR and QFPS. The
information to be collected will also
allow CDC and OPA to improve family
planning-related public health practice,
as CDC and OPA will tailor future
dissemination activities, and develop
needed provider tools, based upon the

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results. CDC will consider conducting a
follow-up information collection
approximately three years after the
baseline survey.
For the baseline information
collection, CDC plans to administer a
mailed survey to a sample of 13,125
private- and public-sector family
planning providers and clinic
administrators in the United States.
Private-sector providers will be
randomly selected from sampling
frames with individual-level
information on providers. To reach
public-sector providers and clinic
administrators, publicly funded clinics
will be randomly selected; one provider
and the clinic administrator will be
asked to complete surveys at sampled
clinics. Specifically, surveys will be
completed by: (a) 3,125 private-sector
office-based physicians (i.e., those
specializing in obstetrics/gynecology,
family medicine, and adolescent
medicine), sampled from the American
Medical Association Physician
Masterfile; (b) 2,000 private-sector midlevel providers (i.e., nurse practitioners
in women’s health and certified nurse
midwives), sampled from the Nurse
Practitioners in Women’s Health
(NPWH) and the American College of
Nurse Midwives (ACNM) membership
lists; (c) 2,000 providers from Title X
clinics, sampled from the Guttmacher
Institute database of publicly funded
family planning clinics; (d) 2,000
providers from non-Title X clinics,
sampled from the Guttmacher Institute
database of publicly funded family
planning clinics; (e) 2,000 clinic
administrators from Title X clinics,
sampled from the Guttmacher Institute
database of publicly funded family
planning clinics; and (f) 2,000 clinic
administrators from non-Title X clinics,
sampled from the Guttmacher Institute
database of publicly funded family
planning clinics.
Each sampled provider and clinic will
receive a mailed survey package. For
private-sector family planning
providers, each mailed survey package
will include a single survey to be
completed by the provider. For publicsector clinics, each mailed survey
package will include two surveys—one
to be completed by a randomly selected
family planning provider at the clinic,
and the second to be completed by the
clinic administrator. Each mailed survey
will be accompanied by a postage-paid
return envelope. Individuals will also be
given the option to complete the survey
online via a password protected webbased data collection system.
Participation in the survey will be
completely voluntary. OMB approval is
requested for one year.

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21102

Federal Register / Vol. 77, No. 68 / Monday, April 9, 2012 / Notices

There are no costs to respondents
other than their time.

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Dated: April 3, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity, Office
of the Associate Director for Science (OADS),
Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2012–8448 Filed 4–6–12; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Child Welfare Demonstration
Projects Information Collection.
OMB No.: New.
Description: Per section 1130 of the
Social Security Act as amended by
Public Law 112–34, the Administration
for Children and Families (ACF),
Administration on Children, Youth and
Families (ACYF), Children’s Bureau
(CB) is planning to announce an

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opportunity for title IV–E agencies to
submit proposals for new child welfare
waiver demonstration projects. CB is
able to approve up to ten child welfare
waiver demonstration projects in each
of Fiscal Years 2012, 2013 and 2014.
These waiver demonstration projects
involve the waiver of certain
requirements of title IV–E and IV–B.
These projects do not provide additional
funding to carry out new services; rather
they allow more flexible uses of Federal
funds in order to test new approaches to
service delivery or financing structures
in an effort to improve outcomes for
children and families involved in the
child welfare system. We encourage title
IV–E agencies wishing to apply for
approval of a waiver demonstration
project to submit a letter of intent
followed by a full proposal at a later
date. For title IV–E agencies that choose
to submit a letter of intent, the letter of
intent should indicate the title IV–E
agency’s intent to submit a proposal,
and briefly describe the demonstration
project, including the nature of the
intervention the agency wishes to

implement, the target population the
agency wishes to serve, the reasons for
selecting the proposed project and the
evaluation design that the agency is
considering. The full proposal must
describe the project in extensive detail
including the goals identified in statute
that the project is intended to
accomplish, the geographic areas in
which the proposed project will be
conducted, the service interventions to
be implemented, the impact
intervention is expected to have on
outcomes related to safety, permanency,
well-being, how service provision will
change for children and families under
the waiver demonstration, a statement
of program requirements for waivers
needed to conduct the project, an
estimate of the projected costs or
savings of the proposed project, a
description of the proposed evaluation
design and an accounting of any other
sources of funding that have been used
to provide the services that the agency
now proposes to address under a waiver
demonstration.
Respondents: State Governments.

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