Agency Forms Undergoing Paperwork Reduction Act Review, 40360-40361 [2012-16647]
Download as PDF
40360
Federal Register / Vol. 77, No. 131 / Monday, July 9, 2012 / Notices
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 provided
additional support for the expansion of
tobacco quitline services and
established a National Quitline Data
Warehouse (NDQW) to collect
information from the 50 states, the
District of Columbia, Puerto Rico, and
Guam. The principal information
collection is based on a uniform
Minimum Data Set (MDS) developed
collaboratively by the North American
Quitline Consortium and other tobacco
control organizations.
Currently, the National Quitline Data
Warehouse is an ongoing data collection
that continues to standardize services,
individual-level intake, and follow-up
data collected by CDC-funded quitlines
for the purposes of program monitoring,
evaluation, and improvement. CDC is
requesting OMB approval to continue
the National Quitline Data Warehouse to
evaluate the impact of Affordable Care
Act, Prevention and Public Health
Funds, and other CDC funding streams,
such as the National Tobacco Control
Program.
Quitline service providers use a
common interview instrument to collect
intake 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 are asked to participate in a
short, voluntary follow-up interview
seven months after intake. Individuallevel data (intake and 7-month followup) are submitted to CDC electronically
through a secure FTP server (60%) and
via U.S. mail (40%).
In addition, CDC collects a web-based
quarterly report about each quitline
program from the designated Tobacco
Control Manager. These reports are used
to quantify changes in service provision
and improvements in the capacity of the
quitlines to assist tobacco users over
time. The majority of these data (90%)
are submitted through the web-based
survey, while the remaining 10% are
submitted through other electronic
means (i.e. email, PDF, fax). Based on
NQDW data collected during the first
two-year OMB clearance period, the
estimated burden per response for the
NQDW Quitline Services Online Survey
is being increased from 7 minutes to 20
minutes.
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. CDC received
public comments about uses of NQDW
data, and other issues, in response to
publication of the 60-day Federal
Register Notice. In response to those
comments, the revision request includes
additional information about uses of
information collected through the
NQDW and describes CDC’s plans to
establish an evaluation working group
to further enhance uses of NQDW data.
Information will be collected
electronically and through the U.S. mail
for a three-year period. There are no
costs to respondents other than their
time. The total estimated annualized
burden hours are 88,982.
ESTIMATED ANNUALIZED BURDEN HOURS
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 ........................
NQDW Intake Questionnaire ....................
1
1/60
510,768
1
10/60
NQDW 7–Month Follow-up Questionnaire
28,900
1
7/60
NQDW Quitline Services Online Survey ..
53
4
20/60
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[FR Doc. 2012–16648 Filed 7–6–12; 8:45 am]
[30Day–12–0821]
sroberts on DSK5SPTVN1PROD with NOTICES
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.
VerDate Mar<15>2010
16:20 Jul 06, 2012
Jkt 226001
Average burden
per response
(in hours)
24,688
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.
BILLING CODE 4163–18–P
Number of
responses per
respondent
Number of
respondents
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
chapter 35). To request a copy of these
requests, call (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC 20503 or by fax to (202) 395–5806.
Written comments should be received
within 30 days of this notice.
Proposed Project
Quarantine Station Illness and Death
Investigation Forms—Airline, Maritime,
Land/Border Crossing Illness and Death
Investigation Forms—Revision—
National Center for Zoonotic and
Emerging Infectious Diseases (NCEZID)
E:\FR\FM\09JYN1.SGM
09JYN1
Federal Register / Vol. 77, No. 131 / Monday, July 9, 2012 / Notices
(0920–0821, expires 9/30/2012), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
CDC is requesting a revision to an
existing data collection of patient-level
clinical, epidemiologic, and
demographic data from ill travelers and
their possible contacts in order to fulfill
its regulatory responsibility to prevent
the importation of communicable
diseases from foreign countries (42 CFR
part 71) and interstate control of
communicable diseases in humans (42
CFR part 70).
Section 361 of the Public Health
Service (PHS) Act (42 U.S.C. 264)
authorizes the Secretary of Health and
Human Services to make and enforce
regulations necessary to prevent the
introduction, transmission or spread of
communicable diseases from foreign
countries into the United States. The
regulations that implement this law, 42
CFR parts 70 and 71, authorize
quarantine officers and other personnel
to inspect and undertake necessary
control measures with respect to
conveyances (e.g., airplanes, cruise
ships, trucks, etc.), persons, and
shipments of animals and etiologic
agents in order to protect the public
health. The regulations also require
conveyances to immediately report an
‘‘ill person’’ or any death on board to
the Quarantine Station prior to arrival in
the United States. An ‘‘ill person’’ is
defined in statute by:
sroberts on DSK5SPTVN1PROD with NOTICES
—Fever (≥100 °F or 38 °C) persisting ≥48
hours.
—Fever (≥100 °F or 38 °C) AND rash,
glandular swelling, or jaundice.
—Diarrhea (≥3 stools in 24 hours or greater
than normal amount).
The 2003 SARS situation and concern
about pandemic influenza and other
communicable diseases have prompted
CDC Quarantine Stations to recommend
that all illnesses be reported prior to
arrival.
CDC Quarantine Stations are currently
located at 20 international U.S. Ports of
Entry. When a suspected illness is
reported to the Quarantine Station,
officers promptly respond to this report
by meeting the incoming conveyance in
person (when possible), collecting
information and evaluating the
patient(s), and determining whether an
ill person can safely be admitted into
the U.S. If Quarantine Station staff are
unable to meet the conveyance, the crew
or medical staff of the conveyance are
trained to complete the required
documentation and forward it (using a
secure system) to the Quarantine Station
for review and follow-up.
VerDate Mar<15>2010
16:20 Jul 06, 2012
Jkt 226001
To perform these tasks in a
streamlined manner and ensure that all
relevant information is collected in the
most efficient and timely manner
possible, Quarantine Stations use a
number of forms—the Air Travel Illness
or Death Investigation Form, Maritime
Conveyance Illness or Death
Investigation Form, and the Land Travel
Illness or Death Investigation Form—to
collect data on passengers with
suspected illness and other travelers/
crew who may have been exposed to an
illness. These forms are also used to
respond to a report of a death aboard a
conveyance.
The purpose of all three forms is the
same: To collect information that helps
quarantine officials detect and respond
to potential public health
communicable disease threats. All three
forms collect the following categories of
information: Demographics and mode of
transportation, clinical and medical
history, and any other relevant facts
(e.g., travel history, traveling
companions, etc.). As part of this
documentation, quarantine public
health officers look for specific signs
and symptoms common to the nine
quarantinable diseases (Pandemic
influenza; SARS; Cholera; Plague;
Diphtheria; Infectious Tuberculosis;
Smallpox; Yellow fever; and Viral
Hemorrhagic Fevers), as well as most
communicable diseases in general.
These signs and symptoms include
fever, difficulty breathing, shortness of
breath, cough, diarrhea, jaundice, or
signs of a neurological infection. The
forms also collect data specific to the
traveler’s conveyance.
These data are used by Quarantine
Stations to make decisions about a
passenger’s suspected illness as well as
its communicability. This in turn
enables Quarantine Station staff to assist
conveyances in the public health
management of passengers and crew.
The estimated total burden on the
public, included in the chart below, can
vary a great deal depending on the
severity of the illness being reported,
the number of contacts, the number of
follow-up inquiries required, and who is
recording the information (e.g.,
Quarantine Station staff versus the
conveyance medical authority). In all
cases, Quarantine Stations have
implemented practices and procedures
that balance the health and safety of the
American public against the public’s
desire for minimal interference with
their travel and trade. Whenever
possible, Quarantine Station staff obtain
information from other documentation
(e.g., manifest order, other airline
documents) to reduce the amount of the
public burden. The total estimated
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
40361
burden requested for this data collection
is 377 hours.
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.
[FR Doc. 2012–16647 Filed 7–6–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–12–0556]
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) 639–7570 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
Assisted Reproductive Technology
(ART) Program Reporting System (0920–
0559, exp. 9/30/2012)—Revision—
National Center for Chronic Disease and
Public Health Promotion (NCDDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The ART program reporting system is
used to comply with Section 2(a) of Pub.
L. 102–493 (known as the Fertility
Clinic Success Rate and Certification
Act of 1992 (FCSRCA)), 42 U.S.C. 263a–
1(a)). FCSRCA requires each ART
program to annually report to the
Secretary through the CDC pregnancy
success rates achieved by each ART
program, the identity of each embryo
laboratory used by such ART program,
and whether the laboratory is certified
or has applied for certification under the
Act. The reporting system allows CDC to
publish an annual success rate report to
Congress as specified by the FCSRCA.
CDC requests OMB approval to
continue information collection for
three years. This Revision request
includes an increase in the total
estimated burden hours due to an
increase in the estimated number of
E:\FR\FM\09JYN1.SGM
09JYN1
Agencies
[Federal Register Volume 77, Number 131 (Monday, July 9, 2012)]
[Notices]
[Pages 40360-40361]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-16647]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-12-0821]
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
(404) 639-7570 or send an email to omb@cdc.gov. Send written comments
to CDC Desk Officer, Office of Management and Budget, Washington, DC
20503 or by fax to (202) 395-5806. Written comments should be received
within 30 days of this notice.
Proposed Project
Quarantine Station Illness and Death Investigation Forms--Airline,
Maritime, Land/Border Crossing Illness and Death Investigation Forms--
Revision--National Center for Zoonotic and Emerging Infectious Diseases
(NCEZID)
[[Page 40361]]
(0920-0821, expires 9/30/2012), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
CDC is requesting a revision to an existing data collection of
patient-level clinical, epidemiologic, and demographic data from ill
travelers and their possible contacts in order to fulfill its
regulatory responsibility to prevent the importation of communicable
diseases from foreign countries (42 CFR part 71) and interstate control
of communicable diseases in humans (42 CFR part 70).
Section 361 of the Public Health Service (PHS) Act (42 U.S.C. 264)
authorizes the Secretary of Health and Human Services to make and
enforce regulations necessary to prevent the introduction, transmission
or spread of communicable diseases from foreign countries into the
United States. The regulations that implement this law, 42 CFR parts 70
and 71, authorize quarantine officers and other personnel to inspect
and undertake necessary control measures with respect to conveyances
(e.g., airplanes, cruise ships, trucks, etc.), persons, and shipments
of animals and etiologic agents in order to protect the public health.
The regulations also require conveyances to immediately report an ``ill
person'' or any death on board to the Quarantine Station prior to
arrival in the United States. An ``ill person'' is defined in statute
by:
--Fever (>=100 [deg]F or 38 [deg]C) persisting >=48 hours.
--Fever (>=100 [deg]F or 38 [deg]C) AND rash, glandular swelling, or
jaundice.
--Diarrhea (>=3 stools in 24 hours or greater than normal amount).
The 2003 SARS situation and concern about pandemic influenza and
other communicable diseases have prompted CDC Quarantine Stations to
recommend that all illnesses be reported prior to arrival.
CDC Quarantine Stations are currently located at 20 international
U.S. Ports of Entry. When a suspected illness is reported to the
Quarantine Station, officers promptly respond to this report by meeting
the incoming conveyance in person (when possible), collecting
information and evaluating the patient(s), and determining whether an
ill person can safely be admitted into the U.S. If Quarantine Station
staff are unable to meet the conveyance, the crew or medical staff of
the conveyance are trained to complete the required documentation and
forward it (using a secure system) to the Quarantine Station for review
and follow-up.
To perform these tasks in a streamlined manner and ensure that all
relevant information is collected in the most efficient and timely
manner possible, Quarantine Stations use a number of forms--the Air
Travel Illness or Death Investigation Form, Maritime Conveyance Illness
or Death Investigation Form, and the Land Travel Illness or Death
Investigation Form--to collect data on passengers with suspected
illness and other travelers/crew who may have been exposed to an
illness. These forms are also used to respond to a report of a death
aboard a conveyance.
The purpose of all three forms is the same: To collect information
that helps quarantine officials detect and respond to potential public
health communicable disease threats. All three forms collect the
following categories of information: Demographics and mode of
transportation, clinical and medical history, and any other relevant
facts (e.g., travel history, traveling companions, etc.). As part of
this documentation, quarantine public health officers look for specific
signs and symptoms common to the nine quarantinable diseases (Pandemic
influenza; SARS; Cholera; Plague; Diphtheria; Infectious Tuberculosis;
Smallpox; Yellow fever; and Viral Hemorrhagic Fevers), as well as most
communicable diseases in general. These signs and symptoms include
fever, difficulty breathing, shortness of breath, cough, diarrhea,
jaundice, or signs of a neurological infection. The forms also collect
data specific to the traveler's conveyance.
These data are used by Quarantine Stations to make decisions about
a passenger's suspected illness as well as its communicability. This in
turn enables Quarantine Station staff to assist conveyances in the
public health management of passengers and crew.
The estimated total burden on the public, included in the chart
below, can vary a great deal depending on the severity of the illness
being reported, the number of contacts, the number of follow-up
inquiries required, and who is recording the information (e.g.,
Quarantine Station staff versus the conveyance medical authority). In
all cases, Quarantine Stations have implemented practices and
procedures that balance the health and safety of the American public
against the public's desire for minimal interference with their travel
and trade. Whenever possible, Quarantine Station staff obtain
information from other documentation (e.g., manifest order, other
airline documents) to reduce the amount of the public burden. The total
estimated burden requested for this data collection is 377 hours.
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.
[FR Doc. 2012-16647 Filed 7-6-12; 8:45 am]
BILLING CODE 4163-18-P