Agency Forms Undergoing Paperwork Reduction Act Review, 1504-1505 [2015-00230]
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1504
Federal Register / Vol. 80, No. 7 / Monday, January 12, 2015 / Notices
and Budget, Washington, DC 20503 or
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Proposed Project
[30Day–15–14KE]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (b) Evaluate the
accuracy of the agencies estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected; (d) Minimize the burden of
the collection of information on those
who are to respond, including through
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and (e) Assess information
collection costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Written
comments and/or suggestions regarding
the items contained in this notice
should be directed to the Attention:
CDC Desk Officer, Office of Management
A Comprehensive Evaluation of a
Paid Social Media and Mass Media
Gynecologic Cancer Campaign—New—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
As authorized by The Gynecologic
Cancer Education and Awareness Act,
CDC currently manages the ‘‘Inside
Knowledge: Get the Facts About
Gynecologic Cancer’’ media campaign.
The campaign seeks to increase
women’s intentions to seek medical
attention for symptoms that could be
indicative of gynecologic cancer.
CDC plans to conduct an evaluation of
the Inside Knowledge (IK) campaign by
collecting information from the target
audience of women ages 40–65 in four
cities (Milwaukee, Wisconsin;
Cincinnati, Ohio; Las Vegas, Nevada
and San Antonio, Texas). In two of the
cities (Milwaukee and San Antonio), the
national IK campaign will be augmented
by an additional paid media campaign.
Evaluation information will be collected
at two time points in each city (a precampaign survey plus one additional
post-campaign survey after the media
intervention). Separate cross-sectional
samples of new respondents will
participate at each point in time. This
will allow CDC to assess exposure to
campaign messages as a function of
media ‘‘dose’’ and to assess whether
women who reside in cities with
additional paid media have higher
awareness of the campaign, higher
knowledge of gynecological cancers,
and greater intentions to seek medical
attention for gynecologic cancer
symptoms and/or to discuss symptoms
with their doctor. CDC initially
considered a more complex evaluation
strategy that involved four waves of data
collection in each city coinciding with
the release of various combinations of
digital media and traditional media. The
current campaign evaluation strategy is
based on a simplified design that allows
CDC to assess main campaign effects
with a smaller number of respondents.
Respondents will be recruited from a
national opt-in online survey panel that
prescreens participants and increases
the likelihood that they meet eligibility
criteria and live within the cities where
the media campaigns are implemented.
The total number of respondents in each
study location is approximately 606
(303 respondents who participate in the
pre-campaign information collection,
and 303 respondents who participate in
the post-campaign information
collection). The target number of
completed responses for the overall
campaign evaluation study is 2,424. The
estimated number of incomplete
responses (individuals who drop out
during or after completion of the
Screening Section of the survey) is 606.
Potential respondents will receive an
email invitation that describes the study
and provides a link to the survey Web
site. Information will then be collected
through self-administered, Web-based
surveys. Survey items will include
measures of audience recall of the
campaign; perceptions of campaign
messages; gynecologic health related
knowledge, attitudes, and beliefs;
intentions to seek care for symptoms
associated gynecologic cancers; and
sociodemographic characteristics.
Results of this evaluation study will
be used to inform CDC, policymakers,
prevention practitioners, researchers,
and the general U.S. population about
the reach and impact of the Inside
Knowledge gynecologic health
awareness campaign, and to inform the
development and implementation of
future health communication efforts.
OMB approval is requested for one
year. The same survey instrument will
be used for all information collection.
Participation is voluntary and there are
no costs to respondents other than their
time. The total estimated burden hours
are 838.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
tkelley on DSK3SPTVN1PROD with NOTICES
Type of respondents
Form name
Women Ages 45–60 in Milwaukee, Cincinnati, Las Vegas, or San Antonio.
Women’s Health Survey (Screening Section
only).
Women’s Health Survey (complete) ..............
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E:\FR\FM\12JAN1.SGM
Number of
responses per
respondent
Average
burden per
response
(in hours)
606
1
3/60
2,424
1
20/60
12JAN1
Federal Register / Vol. 80, No. 7 / Monday, January 12, 2015 / Notices
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2015–00230 Filed 1–9–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Proposed Project
[60Day–15–0792]
tkelley on DSK3SPTVN1PROD with NOTICES
Proposed Data Collections Submitted
for Public Comment and
Recommendations
The Centers for Disease Control and
Prevention (CDC), as part of its
continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. To request more
information on the below proposed
project or to obtain a copy of the
information collection plan and
instruments, call 404–639–7570 or send
comments to LeRoy Richardson, 1600
Clifton Road, MS–D74, Atlanta, GA
30333 or send an email to omb@cdc.gov.
Comments submitted in response to
this notice will be summarized and/or
included in the request for Office of
Management and Budget (OMB)
approval. 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; (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; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
VerDate Sep<11>2014
17:35 Jan 09, 2015
Jkt 235001
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information. Written comments should
be received within 60 days of this
notice.
Environmental Health Specialists
Network (EHS-NET) Program (OMB No.
0920–0792, expires 2/28/2015)—
Revision—National Center for
Environmental Health (NCEH), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
The CDC is requesting OMB approval
for three additional years to use this
generic clearance for a research program
focused on identifying the
environmental causes of foodborne
illness.
To date, EHS-Net has conducted four
studies under this generic clearance.
The first study collected data on
improper cooling of hot foods, a food
handling practice associated with
foodborne illness and outbreaks. The
second study collected data on the
relationship between kitchen manager
food safety certification and foodborne
illness risk factors in restaurants. Public
health agencies are increasingly
encouraging or requiring certification as
a foodborne illness prevention measure,
yet little is known about its
effectiveness. The third study collected
data on the environmental factors
associated with contamination of the
retail deli environment with Listeria, a
foodborne illness pathogen ranked 3rd
in terms of the number of deaths it
causes. The fourth study collected data
on restaurant managers’ and workers’
food allergen knowledge, attitudes, and
practices. Food allergens are an
important food safety issue for
restaurants.
The data from the first two studies
have been disseminated to
environmental public health/food safety
regulatory programs and the food
industry in the form of presentations at
conferences and meetings, scientific
journal publications, and Web site
postings. We will continue to analyze
and present the data from all four
studies, and expect that they will
continue to provide valuable and useful
data about environmental factors
PO 00000
Frm 00013
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1505
associated with foodborne illness
outbreaks and food safety issues.
This revision will provide OMB
clearance for EHS-Net data collections
conducted in 2015 through 2018
(approximately one per year). The
program is revising the generic
information collection request (ICR) in
the following ways:
(1) Because of the re-announcement
and re-competition of the EHS-Net
cooperative agreement in 2015, it is
likely that the sites in which data will
be collected will differ from the sites in
which data were collected previously.
(2) We revised the estimated study
sample size and burden downward.
Thus, the estimated burden has been
reduced.
(3) We have eliminated proposed
sample weighting analyses.
Reducing foodborne illness first
requires identification and
understanding of the environmental
factors that cause these illnesses. We
need to know how and why food
becomes contaminated with foodborne
illness pathogens. This information can
then be used to determine effective food
safety prevention methods. Ultimately,
these actions can lead to increased
regulatory program effectiveness and
decreased foodborne illness. The
purpose of this food safety research
program is to identify and understand
environmental factors associated with
foodborne illness and outbreaks. This
program is conducted by the
Environmental Health Specialists
Network (EHS-Net), a collaborative
project of CDC, FDA, USDA, and local
and state sites.
Environmental factors associated with
foodborne illness include both food
safety practices (e.g., inadequate
cleaning practices) and the factors in the
environment associated with those
practices (e.g., worker and retail food
establishment characteristics). To
understand these factors, we need to
continue to collect data from those who
prepare food (i.e., food workers) and on
the environments in which the food is
prepared (i.e., retail food establishment
kitchens). Thus, data collection methods
for this generic package include: (1)
Manager and worker interviews/
surveys, and (2) observation of kitchen
environments. Both methods allow data
collection on food safety practices and
environmental factors associated with
those practices.
For each data collection, we will
collect data in approximately 47 retail
food establishments per site. Thus, there
will be approximately 376
establishments per data collection (an
estimated 8 sites × 47 establishments).
We expect a manager/establishment
E:\FR\FM\12JAN1.SGM
12JAN1
Agencies
[Federal Register Volume 80, Number 7 (Monday, January 12, 2015)]
[Notices]
[Pages 1504-1505]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-00230]
[[Page 1504]]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-15-14KE]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has submitted
the following information collection request to the Office of
Management and Budget (OMB) for review and approval in accordance with
the Paperwork Reduction Act of 1995. The notice for the proposed
information collection is published to obtain comments from the public
and affected agencies.
Written comments and suggestions from the public and affected
agencies concerning the proposed collection of information are
encouraged. Your comments should address any of the following: (a)
Evaluate whether the proposed collection of information is necessary
for the proper performance of the functions of the agency, including
whether the information will have practical utility; (b) Evaluate the
accuracy of the agencies estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (c) Enhance the quality, utility, and clarity of
the information to be collected; (d) Minimize the burden of the
collection of information on those who are to respond, including
through the use of appropriate automated, electronic, mechanical, or
other technological collection techniques or other forms of information
technology, e.g., permitting electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570 or send an email to omb@cdc.gov. Written comments and/or
suggestions regarding the items contained in this notice should be
directed to the Attention: 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
A Comprehensive Evaluation of a Paid Social Media and Mass Media
Gynecologic Cancer Campaign--New--National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
As authorized by The Gynecologic Cancer Education and Awareness
Act, CDC currently manages the ``Inside Knowledge: Get the Facts About
Gynecologic Cancer'' media campaign. The campaign seeks to increase
women's intentions to seek medical attention for symptoms that could be
indicative of gynecologic cancer.
CDC plans to conduct an evaluation of the Inside Knowledge (IK)
campaign by collecting information from the target audience of women
ages 40-65 in four cities (Milwaukee, Wisconsin; Cincinnati, Ohio; Las
Vegas, Nevada and San Antonio, Texas). In two of the cities (Milwaukee
and San Antonio), the national IK campaign will be augmented by an
additional paid media campaign. Evaluation information will be
collected at two time points in each city (a pre-campaign survey plus
one additional post-campaign survey after the media intervention).
Separate cross-sectional samples of new respondents will participate at
each point in time. This will allow CDC to assess exposure to campaign
messages as a function of media ``dose'' and to assess whether women
who reside in cities with additional paid media have higher awareness
of the campaign, higher knowledge of gynecological cancers, and greater
intentions to seek medical attention for gynecologic cancer symptoms
and/or to discuss symptoms with their doctor. CDC initially considered
a more complex evaluation strategy that involved four waves of data
collection in each city coinciding with the release of various
combinations of digital media and traditional media. The current
campaign evaluation strategy is based on a simplified design that
allows CDC to assess main campaign effects with a smaller number of
respondents.
Respondents will be recruited from a national opt-in online survey
panel that prescreens participants and increases the likelihood that
they meet eligibility criteria and live within the cities where the
media campaigns are implemented. The total number of respondents in
each study location is approximately 606 (303 respondents who
participate in the pre-campaign information collection, and 303
respondents who participate in the post-campaign information
collection). The target number of completed responses for the overall
campaign evaluation study is 2,424. The estimated number of incomplete
responses (individuals who drop out during or after completion of the
Screening Section of the survey) is 606.
Potential respondents will receive an email invitation that
describes the study and provides a link to the survey Web site.
Information will then be collected through self-administered, Web-based
surveys. Survey items will include measures of audience recall of the
campaign; perceptions of campaign messages; gynecologic health related
knowledge, attitudes, and beliefs; intentions to seek care for symptoms
associated gynecologic cancers; and sociodemographic characteristics.
Results of this evaluation study will be used to inform CDC,
policymakers, prevention practitioners, researchers, and the general
U.S. population about the reach and impact of the Inside Knowledge
gynecologic health awareness campaign, and to inform the development
and implementation of future health communication efforts.
OMB approval is requested for one year. The same survey instrument
will be used for all information collection. Participation is voluntary
and there are no costs to respondents other than their time. The total
estimated burden hours are 838.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondents Form name respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Women Ages 45-60 in Milwaukee, Women's Health Survey 606 1 3/60
Cincinnati, Las Vegas, or San (Screening Section only).
Antonio.
Women's Health Survey 2,424 1 20/60
(complete).
----------------------------------------------------------------------------------------------------------------
[[Page 1505]]
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2015-00230 Filed 1-9-15; 8:45 am]
BILLING CODE 4163-18-P