Agency Information Collection Activities; Submission for OMB Review; Comment Request; Alzheimer's Disease Demonstration Grants to States Program Standardized Data Collection, 7040-7041 [E7-2545]
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7040
Federal Register / Vol. 72, No. 30 / Wednesday, February 14, 2007 / Notices
bank’s records. This program should
include a requirement to install security
devices and should establish procedures
that satisfy minimum standards in the
regulation, with the security officer
determining the need for additional
security devices and procedures based
on the location of the banking office.
There is no formal reporting form and
the information is not submitted to the
Federal Reserve.
Current Actions: On December 4,
2006, the Federal Reserve published a
notice in the Federal Register (71 FR
70392) requesting public comment for
60 days on the extension, without
revision, of the Written Security
Program for State Member Banks. The
comment period for this notice expired
on February 2, 2007. The Federal
Reserve did not receive any comments.
Board of Governors of the Federal Reserve
System, February 8, 2007.
Jennifer J. Johnson
Secretary of the Board
[FR Doc. E7–2484 Filed 2–13–07; 8:45 am]
from the National Information Center
website at www.ffiec.gov/nic/.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than March 13,
2007.
A. Federal Reserve Bank of St. Louis
(Glenda Wilson, Community Affairs
Officer) 411 Locust Street, St. Louis,
Missouri 63166-2034:
1. Cabool State Bank Employee Stock
Ownership Plan, Cabool, Missouri; to
acquire an additional 2 percent of the
voting shares, for total ownership of
30.36 percent, of Cabool Bancshares,
Inc., Cabool, Missouri, and thereby
indirectly acquire Cabool State Bank,
Cabool, Missouri.
Board of Governors of the Federal Reserve
System, February 9, 2007.
Jennifer J. Johnson,
Secretary of the Board.
[FR Doc. E7–2517 Filed 2–13–07; 8:45 am]
BILLING CODE 6210–01–S
BILLING CODE 6210–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
ycherry on PROD1PC64 with PRELIMS
FEDERAL RESERVE SYSTEM
Administration on Aging
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR Part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The application also will be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Additional information on all bank
holding companies may be obtained
VerDate Aug<31>2005
17:27 Feb 13, 2007
Jkt 211001
Agency Information Collection
Activities; Submission for OMB
Review; Comment Request;
Alzheimer’s Disease Demonstration
Grants to States Program Standardized
Data Collection
Administration on Aging, HHS.
Notice.
AGENCY:
ACTION:
SUMMARY: The Administration on Aging
(AoA) is announcing that the proposed
collection of information listed below
has been submitted to the Office of
Management and Budget (OMB) for
review and clearance under the
Paperwork Reduction Act of 1995.
DATES: Submit written comments on the
collection of information by March 16,
2007.
ADDRESSES: Submit written comments
on the collection of information by fax
202.395.6974 or by mail to the Office of
Information and Regulatory Affairs,
OMB, New Executive Office Bldg., 725
17th St. NW., rm. 10235, Washington,
DC 20503, Attn: Carolyn Lovett, Desk
Officer for AoA.
FOR FURTHER INFORMATION CONTACT: Lori
Stalbaum at 202–357–3452 or e-mail:
lori.stalbaum@aoa.hhs.gov
In
compliance with 44 U.S.C. 3507, AoA
has submitted the following proposed
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
collection of information to OMB for
review and clearance.
The Alzheimer’s Disease
Demonstration Grants to States
(ADDGS) Program is authorized through
Sections 398, 399 and 399A of the
Public Health Service (PHS) Act, as
amended by Public Law 101–557 Home
Health Care and Alzheimer’s Disease
Amendments of 1990. The ADDGS
program funded through AoA helps
states extend family support services
provided by subgrantees to underserved
populations, including those in rural
communities.
The PHS Act requires AoA to
‘‘provide for an evaluation of each
demonstration project for which a grant
is made.’’ The PHS Act further states
that ‘‘not later than 6 months after the
completion of such evaluations, submit
a report to the Congress describing the
findings made as a result of the
evaluations.’’ In compliance with the
PHS Act, AoA developed a new State
data collection protocol that will require
future ADDGS state grantees (those
funded starting in FY 2007) to transmit
annual data information to AoA
reported to the states by the project
partners.
Many of the elements for the ADDGS
Data Program Report are the same as
those collected for Older Americans Act
Title III and Title VII programs
administered by AoA. To ensure
inclusion of essential information the
ADDGS Project Officer first contacted
all current ADDGS grantees to find out
what type of information they are
already collecting. Then, the ADDGS
Project Officer solicited information on
key data elements from experts familiar
with the previous ADDGS Program
evaluation. Following this input,
modifications were made to the data
collection tool and input was solicited
from all ADDGS state Project Directors
and their project partners. Twenty-three
(23) of thirty-eight (38) states,
approximately 60% responded to the
request for feedback. Again,
modifications were made to fine tune
the data collection tool into a format
that would minimize burden on state
grantees. Finally, ten (10) ADDGS
Project Directors participated in a
telephone focus group. The ten Project
Directors were selected based on the
detail of their responses to the original
request for feedback.
The result of this input is the
proposed data collection tool and
accompanying definition of terms. AoA
is aware that different states have
different capabilities in terms of data
collection. Thus, it is understood that
following the approval of the proposed
ADDGS data collection tool, AoA will
E:\FR\FM\14FEN1.SGM
14FEN1
7041
Federal Register / Vol. 72, No. 30 / Wednesday, February 14, 2007 / Notices
need to work with ADDGS grantees to
ensure easy access to a reporting system
as well as offer regular training to state
grantees to ensure minimal burden.
AoA estimates the burden of this
collection of information as follows: 950
hours.
Dated: February 9, 2007.
Josefina G. Carbonell,
Assistant Secretary for Aging.
[FR Doc. E7–2545 Filed 2–13–07; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–07–0255]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC, or by fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
Information Collection of the
Resources and Services Database of the
National Prevention Information
Network-Extension—National Center for
HIV, STD, & TB Prevention (NCHSTP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The National Center for HIV, STD,
and TB Prevention (NCHSTP) proposes
to continue data collection for the
Resources and Services Database on
CDC National Prevention Information
Network.
The CDC, NCHSTP program has the
primary responsibility within the CDC
and the U.S. Public Health Service for
the prevention and control of HIV
infection, sexually transmitted diseases
(STDs), tuberculosis (TB), and related
infections, as well as for communitybased HIV prevention activities, syphilis
and TB elimination programs. To
support NCHSTP’s mission and to link
Americans to prevention, education,
and care services, the CDC National
Prevention Information Network (NPIN)
serves as the U.S. reference, referral, and
distribution service for information on
HIV/AIDS, STDs, and TB. NPIN is a
critical member of the network of
government agencies, community
organizations, businesses, health
professionals, educators, and human
services providers that educate the
American public about the grave threat
to public health posed by HIV/AIDS,
STDs, and TB, and provides services for
persons infected with human
immunodeficiency virus (HIV).
Established in 1988, the NPIN
Resources and Services Database
contains entries on approximately
15,000 organizations and is the most
comprehensive listing of HIV/AIDS,
STD and TB resources and services
available throughout the country. This
database describes national, state and
local organizations that provide services
related to HIV/AIDS, STDs, and TB,
services such as; counseling and testing,
prevention, education and support. The
NPIN reference staff relies on the
Resources and Services Database to
respond to thousands of requests each
year for information or referral from
community based organizations, state
and local health departments, and
health professionals working in HIV/
AIDS, STD and TB prevention. The
CDC–INFO (formerly the CDC National
AIDS Hotline) staff also uses the NPIN
Resources and Services Database to refer
up to 500,000 callers each year to local
programs for information, services, and
treatment. The American public can
also access the NPIN Resources and
Services database through the NPIN
Web site. More than 24 million hits and
2 million visits by the public to the
website are recorded annually.
A representative from each new
organization identified will be
administered the resource organization
questionnaire via the telephone.
Representatives may include registered
nurses, social and community service
managers, health educators, or social
and human service assistants. As part of
the update and verification process for
organizations currently included in the
Resources and Services Database, about
30 percent of the organization’s
representatives will receive a copy of
their current database entry by
electronic mail, including an
introductory message and a list of
instructions. The remaining 70 percent
will receive a telephone call to review
their database record. This request is for
a 3-year renewal of clearance. There are
no costs to respondents other than their
time. The total estimated annual burden
hours are 3,007.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of responses per
respondent
Average
burden per response
(in hours)
125
7,000
3,000
75
1
1
1
1
17/60
10/60
16/60
17/60
Annual Update Request (Telephone) ....................................
Annual Update Request (Email) ............................................
Annual Update Request (Telephone) ....................................
3,220
1,380
280
1
1
1
10/60
16/60
10/60
Annual Update Request (Email) ............................................
120
1
16/60
Type of
respondent
Form
Private Sector Organizations ..
Questionnaire (Telephone Script) ..........................................
Annual Update Request (Telephone) ....................................
Annual Update Request (Email) ............................................
Questionnaire (Telephone Script) ..........................................
State and Local Government
Organizations.
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Federal Government Organizations.
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Number of
respondents
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14FEN1
]]>Agencies
[Federal Register Volume 72, Number 30 (Wednesday, February 14, 2007)]
[Notices]
[Pages 7040-7041]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-2545]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration on Aging
Agency Information Collection Activities; Submission for OMB
Review; Comment Request; Alzheimer's Disease Demonstration Grants to
States Program Standardized Data Collection
AGENCY: Administration on Aging, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration on Aging (AoA) is announcing that the
proposed collection of information listed below has been submitted to
the Office of Management and Budget (OMB) for review and clearance
under the Paperwork Reduction Act of 1995.
DATES: Submit written comments on the collection of information by
March 16, 2007.
ADDRESSES: Submit written comments on the collection of information by
fax 202.395.6974 or by mail to the Office of Information and Regulatory
Affairs, OMB, New Executive Office Bldg., 725 17th St. NW., rm. 10235,
Washington, DC 20503, Attn: Carolyn Lovett, Desk Officer for AoA.
FOR FURTHER INFORMATION CONTACT: Lori Stalbaum at 202-357-3452 or e-
mail: lori.stalbaum@aoa.hhs.gov
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, AoA has
submitted the following proposed collection of information to OMB for
review and clearance.
The Alzheimer's Disease Demonstration Grants to States (ADDGS)
Program is authorized through Sections 398, 399 and 399A of the Public
Health Service (PHS) Act, as amended by Public Law 101-557 Home Health
Care and Alzheimer's Disease Amendments of 1990. The ADDGS program
funded through AoA helps states extend family support services provided
by subgrantees to underserved populations, including those in rural
communities.
The PHS Act requires AoA to ``provide for an evaluation of each
demonstration project for which a grant is made.'' The PHS Act further
states that ``not later than 6 months after the completion of such
evaluations, submit a report to the Congress describing the findings
made as a result of the evaluations.'' In compliance with the PHS Act,
AoA developed a new State data collection protocol that will require
future ADDGS state grantees (those funded starting in FY 2007) to
transmit annual data information to AoA reported to the states by the
project partners.
Many of the elements for the ADDGS Data Program Report are the same
as those collected for Older Americans Act Title III and Title VII
programs administered by AoA. To ensure inclusion of essential
information the ADDGS Project Officer first contacted all current ADDGS
grantees to find out what type of information they are already
collecting. Then, the ADDGS Project Officer solicited information on
key data elements from experts familiar with the previous ADDGS Program
evaluation. Following this input, modifications were made to the data
collection tool and input was solicited from all ADDGS state Project
Directors and their project partners. Twenty-three (23) of thirty-eight
(38) states, approximately 60% responded to the request for feedback.
Again, modifications were made to fine tune the data collection tool
into a format that would minimize burden on state grantees. Finally,
ten (10) ADDGS Project Directors participated in a telephone focus
group. The ten Project Directors were selected based on the detail of
their responses to the original request for feedback.
The result of this input is the proposed data collection tool and
accompanying definition of terms. AoA is aware that different states
have different capabilities in terms of data collection. Thus, it is
understood that following the approval of the proposed ADDGS data
collection tool, AoA will
[[Page 7041]]
need to work with ADDGS grantees to ensure easy access to a reporting
system as well as offer regular training to state grantees to ensure
minimal burden.
AoA estimates the burden of this collection of information as
follows: 950 hours.
Dated: February 9, 2007.
Josefina G. Carbonell,
Assistant Secretary for Aging.
[FR Doc. E7-2545 Filed 2-13-07; 8:45 am]
BILLING CODE 4154-01-P
