Agency Forms Undergoing Paperwork Reduction Act Review, 28620-28621 [2010-12181]
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28620
Federal Register / Vol. 75, No. 98 / Friday, May 21, 2010 / Notices
what studies, if any, are needed before
implementing a policy change; what
monitoring tools or surveillance
activities would need to be in place
before implementing a policy change;
what additional safety measures, if any,
are needed to assure blood safety under
a revised deferral policy?
The public will have opportunity to
present their views to the Committee on
the second day. A public comment
session has been scheduled for June 11,
2010. Comments will be limited to five
minutes per speaker and must be
pertinent to the discussion. Preregistration is required for participation
in the public comment session. Any
member of the public who would like to
participate in this session should
contact the Executive Secretary no later
than June 8, 2010. It is requested that
those who wish to have printed material
distributed to the Committee provide
thirty (30) copies of the document to be
distributed to the Executive Secretary,
ACBSA, prior to close of business June
8, 2010. If it is not possible to provide
30 copies of the material to be
distributed, then individuals are
requested to provide at a minimum one
(1) copy of the document(s) to be
distributed prior to the close of business
June 8, 2010. It also is requested that
any member of the public who wishes
to provide comments to the Committee
utilizing electronic data projection
submit the necessary material to the
Executive Secretary prior to close of
business June 8, 2010. Electronic
comments must adhere to disability
accessibility guidelines (Section 508
compliance).
Dated: May 4, 2010.
Jerry A. Holmberg,
Executive Secretary, Advisory Committee on
Blood Safety and Availability.
[FR Doc. 2010–12326 Filed 5–20–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30 Day–10–10BT]
emcdonald on DSK2BSOYB1PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
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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) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
National Quitline Data Warehouse—
New—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Tobacco use remains the leading
preventable cause of disease and death
in the United States, resulting in
approximately 440,000 deaths annually
and contributing to $92 billion annually
in lost worker productivity. Although
the prevalence of current smoking
among adults decreased significantly
since its peak in the 1960s, overall
smoking prevalence among U.S. adults
has remained virtually unchanged
during the past five years. Large
disparities in smoking prevalence
continue to exist among members of
racial/ethnic minority groups and
individuals of low socioeconomic
status.
The National Tobacco Control
Program (NTCP) was established by
CDC to help reduce tobacco-related
disease, disability, and death. The NTCP
provides funding for state Quitlines,
which provide telephone-based tobacco
cessation services to help tobacco users
quit. Quitlines overcome many of the
barriers to tobacco cessation classes and
traditional clinics because they are free
and available at the caller’s
convenience. Quitline services in all
states can be accessed through a toll-free
national portal number at 1–800–QUIT–
NOW. According to CDC’s Best
Practices for Comprehensive Tobacco
Control, approximately six to eight
percent of tobacco users potentially can
be reached successfully by Quitlines;
however, currently, only one to two
percent of tobacco users contact
Quitlines.
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With funding authorized by the
American Recovery and Reinvestment
Act of 2009 (ARRA), CDC has provided
additional support for the expansion of
tobacco Quitline services. CDC is
therefore requesting OMB approval to
establish a National Quitline Data
Warehouse (NDQW), and to collect
information from the 50 states, the
District of Columbia, Puerto Rico, and
Guam. The principal information
collection will be based on a uniform
Minimum Data Set (MDS) developed
collaboratively by the North American
Quitline Consortium and other tobacco
control organizations.
Quitline service providers will use a
common interview instrument to collect
information from all callers. A oneminute interview will be conducted
with callers who contact the Quitline to
obtain information on another person’s
behalf. Callers who contact the Quitline
to obtain information or services for
themselves will be asked to participate
in a 10-minute interview. A random
sample of callers who receive a Quitline
service will be asked to participate in a
short, voluntary follow-up interview
seven months after intake.
In addition, to monitor and evaluate
the expenditure of Recovery Act
funding, CDC will collect a quarterly
report about each Quitline program from
the designated Tobacco Control
Manager. These reports will be used to
quantify improvements in the capacity
of the Quitlines to assist tobacco users
over time.
The information collected in the
NQDW will be used to determine the
role Quitlines play in promoting tobacco
use cessation, measure the number of
tobacco users being served by state
Quitlines, determine reach of Quitlines
to high-risk populations (e.g., racial and
ethnic minorities and the medically
underserved), measure the number
using each state Quitline who quit,
determine whether some combinations
of services contribute to higher quit
rates than others, and improve the
timeliness, access to, and quality of data
collected by Quitlines.
Information will be collected
electronically for a two-year period.
There are no costs to respondents other
than their time. The total estimated
annualized burden hours are 90,563.
E:\FR\FM\21MYN1.SGM
21MYN1
28621
Federal Register / Vol. 75, No. 98 / Friday, May 21, 2010 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Average
burden per response
(in hours)
230,000
1
1/60
.........................................................................
500,000
1
10/60
Follow-up Questionnaire ................................
Quitline Services Questionnaire .....................
28,900
53
1
4
7/60
7/60
Number of
respondents
Type of respondent
Form name
Caller who contacts the Quitline on behalf of
someone else.
Caller who contacts the Quitline for personal
use.
Quitline caller who received a Quitline service
Tobacco Control Manager ..............................
Intake Questionnaire ......................................
Dated: May 13, 2010.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2010–12181 Filed 5–20–10; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
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
Centers for Disease Control and
Prevention
[60Day–10–10DE]
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)
Creation of state and metropolitan
area-based surveillance projects for
Amyotrophic Lateral Sclerosis (ALS)—
New—Agency for Toxic Substances and
Disease Registry (ATSDR), Coordinating
Center for Environmental Health and
Injury Prevention (CCEHIP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
On October 10, 2008, President Bush
signed S. 1382: ALS Registry Act which
amended the Public Health Service Act
to provide for the establishment of an
Amyotrophic Lateral Sclerosis (ALS)
Registry. The activities described are
part of the effort to create the National
ALS Registry. The purpose of the
registry is to: (1) Better describe the
incidence and prevalence of ALS in the
United States; (2) examine appropriate
factors, such as environmental and
occupational, that might be associated
with the disease; (3) better outline key
demographic factors (such as age, race
or ethnicity, gender, and family history)
associated with the disease; and (4)
better examine the connection between
ALS and other motor neuron disorders
that can be confused with ALS,
misdiagnosed as ALS, and in some cases
progress to ALS. The registry will
collect personal health information that
may provide a basis for further scientific
studies of potential risks for developing
ALS.
This project purposes to collect
information specific data related to ALS.
The objective of this project is to
develop state-based and metropolitan
area-based surveillance projects for
ALS. The primary goal of the state-based
and metropolitan area-based
surveillance project is to use these data
to evaluate the completeness of the
National ALS Registry. The secondary
goal of the surveillance project is to
obtain reliable and timely information
on the incidence and prevalence of ALS
and to better describe the demographic
characteristics (e.g., age, race, sex, and
geographic location) of those with ALS.
Neurologists or their staff will
complete an ALS Case Reporting Form
on each of their ALS patients. This will
be transmitted to the state or
metropolitan health department.
Approval is being requested for a 3-year
period; it is estimated that there will be
approximately 6,750 cases of ALS
reported in the state and metropolitan
areas during this 3-year period. An ALS
Medical Record Verification Form will
be collected on a subset of cases
reported.
Surveillance items to be collected
include information to make sure that
there are no duplicates such as full
name, address, date of birth, and last
five digits of the Social Security
number.
There are no costs to the neurologist
respondents reporting the cases other
than their time.
emcdonald on DSK2BSOYB1PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses
per respondent
Average
burden per
response
(in hours)
Total
burden
hours
Type of respondents
Form
Neurologists ..........................................................
Neurologists ..........................................................
Case Reporting Form ...........................................
Case Verification Form .........................................
2,250
540
5/60
20/60
188
180
Total ......................................................................
...............................................................................
....................
....................
368
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Agencies
[Federal Register Volume 75, Number 98 (Friday, May 21, 2010)]
[Notices]
[Pages 28620-28621]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-12181]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30 Day-10-10BT]
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 e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-5806.
Written comments should be received within 30 days of this notice.
Proposed Project
National Quitline Data Warehouse--New--National Center for Chronic
Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Tobacco use remains the leading preventable cause of disease and
death in the United States, resulting in approximately 440,000 deaths
annually and contributing to $92 billion annually in lost worker
productivity. Although the prevalence of current smoking among adults
decreased significantly since its peak in the 1960s, overall smoking
prevalence among U.S. adults has remained virtually unchanged during
the past five years. Large disparities in smoking prevalence continue
to exist among members of racial/ethnic minority groups and individuals
of low socioeconomic status.
The National Tobacco Control Program (NTCP) was established by CDC
to help reduce tobacco-related disease, disability, and death. The NTCP
provides funding for state Quitlines, which provide telephone-based
tobacco cessation services to help tobacco users quit. Quitlines
overcome many of the barriers to tobacco cessation classes and
traditional clinics because they are free and available at the caller's
convenience. Quitline services in all states can be accessed through a
toll-free national portal number at 1-800-QUIT-NOW. According to CDC's
Best Practices for Comprehensive Tobacco Control, approximately six to
eight percent of tobacco users potentially can be reached successfully
by Quitlines; however, currently, only one to two percent of tobacco
users contact Quitlines.
With funding authorized by the American Recovery and Reinvestment
Act of 2009 (ARRA), CDC has provided additional support for the
expansion of tobacco Quitline services. CDC is therefore requesting OMB
approval to establish a National Quitline Data Warehouse (NDQW), and to
collect information from the 50 states, the District of Columbia,
Puerto Rico, and Guam. The principal information collection will be
based on a uniform Minimum Data Set (MDS) developed collaboratively by
the North American Quitline Consortium and other tobacco control
organizations.
Quitline service providers will use a common interview instrument
to collect information from all callers. A one-minute interview will be
conducted with callers who contact the Quitline to obtain information
on another person's behalf. Callers who contact the Quitline to obtain
information or services for themselves will be asked to participate in
a 10-minute interview. A random sample of callers who receive a
Quitline service will be asked to participate in a short, voluntary
follow-up interview seven months after intake.
In addition, to monitor and evaluate the expenditure of Recovery
Act funding, CDC will collect a quarterly report about each Quitline
program from the designated Tobacco Control Manager. These reports will
be used to quantify improvements in the capacity of the Quitlines to
assist tobacco users over time.
The information collected in the NQDW will be used to determine the
role Quitlines play in promoting tobacco use cessation, measure the
number of tobacco users being served by state Quitlines, determine
reach of Quitlines to high-risk populations (e.g., racial and ethnic
minorities and the medically underserved), measure the number using
each state Quitline who quit, determine whether some combinations of
services contribute to higher quit rates than others, and improve the
timeliness, access to, and quality of data collected by Quitlines.
Information will be collected electronically for a two-year period.
There are no costs to respondents other than their time. The total
estimated annualized burden hours are 90,563.
[[Page 28621]]
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Caller who contacts the Quitline on Intake Questionnaire.... 230,000 1 1/60
behalf of someone else.
Caller who contacts the Quitline for ........................ 500,000 1 10/60
personal use.
Quitline caller who received a Follow-up Questionnaire. 28,900 1 7/60
Quitline service.
Tobacco Control Manager............... Quitline Services 53 4 7/60
Questionnaire.
----------------------------------------------------------------------------------------------------------------
Dated: May 13, 2010.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2010-12181 Filed 5-20-10; 8:45 am]
BILLING CODE 4163-18-P