Proposed Data Collection Submitted for Public Comment and Recommendations, 69680-69681 [2015-28473]
Download as PDF
<![CDATA[
69680
Federal Register / Vol. 80, No. 217 / Tuesday, November 10, 2015 / Notices
Educational Program, Tools, or
Materials to Enhance Self-Management
in Systemic Lupus Erythematosus’’ to
identify and address the needs of lupus
patients in practicing effective selfmanagement. The purpose of this
project is to develop a SLE selfmanagement tool to improve the ability
of people living with lupus to manage
their condition.
The proposed information collection
will assess a SLE self-management tool
that is in development to ensure that the
tool is usable and useful to members of
the target audience. The tool is expected
to be comprised of multiple SLE selfmanagement resources that may
include, but are not limited to:
Education resources about fatigue
management, pain management, healthy
telephone interviews with men with a
diagnosis of SLE will be conducted to
assess the tool. The same discussion
guide will be used for all information
collection. The estimated burden per
response for participating in a focus
group discussion is 2 hours. The
estimated burden per response for a
discussion conducted via telephone
interview is 45 minutes. Respondent
burden also includes 2 hours for
reviewing the draft SLE selfmanagement tool in advance of the
focus group meeting or telephone
interview.
OMB approval is requested for one
year. Participation is voluntary and
there are no costs to respondents other
than their time.
diet, and exercise; symptom trackers;
medication trackers; appointment
calendars; resources about
communication with family, friends,
and co-workers about SLE; and
strategies for coping with depression
and anxiety. CDC plans to make the tool
available in an electronic format (webbased or a native mobile application)
and will consider making it available as
a printed resource, depending on the
feedback obtained during the testing
process.
The information collection will also
gauge the needs of the target
audience(s), tool format and delivery
method(s), and the tool’s clarity,
relevance, salience and appeal. A series
of focus groups with women with a
diagnosis of SLE, and one-on-one
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Number of
respondents
Form name
Average
burden per
response
(in hrs.)
Number of
responses per
respondent
Total burden
(in hrs.)
Women with SLE diagnosis.
Screener ...............................................................
192
1
10/60
32
Men with SLE diagnosis
Review of the CDC SLE Self-Management Tool
Discussion Guide .................................................
Screener ...............................................................
Review of the CDC SLE Self-Management Tool
Discussion Guide .................................................
128
128
40
20
20
1
1
1
2
1
2
2
10/60
2
45/60
256
256
7
40
15
Total .......................
..............................................................................
........................
........................
........................
606
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. 2015–28472 Filed 11–9–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–16CP; Docket No. CDC–2015–
0100]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
asabaliauskas on DSK5VPTVN1PROD with NOTICES
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
SUMMARY:
VerDate Sep<11>2014
19:41 Nov 09, 2015
Jkt 238001
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. This notice invites
comment on a proposed information
collection request entitled ‘‘Data
Collection for Community-based Tick
Control for the Prevention of Rocky
Mountain Spotted Fever in Hermosillo,
Mexico.’’ This project will be carried
out in collaboration with the Rickettsial
Zoonoses Branch, National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC) and the
University of Sonora School of
Medicine (UNSOM) to assess the
efficacy and impact of a community
based tick prevention project.
DATES: Written comments must be
received on or before January 11, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0100 by any of the following methods:
• Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
PO 00000
Frm 00049
Fmt 4703
Sfmt 4703
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
FOR FURTHER INFORMATION CONTACT:
E:\FR\FM\10NON1.SGM
10NON1
69681
Federal Register / Vol. 80, No. 217 / Tuesday, November 10, 2015 / Notices
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
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
The information collection for which
approval is sought is in accordance with
RZB’s mission to reduce morbidity and
mortality of rickettsial diseases and
decrease the burden of disease through
control and prevention methods.
Authorizing Legislation comes from
section 301 of the Public Health Service
Act (42 U.S.C. 241).
Approval for a three-year data
collection will allow RZB to collect
information related to risk of RMSF to
improve and inform prevention
activities. Successful execution of RZB’s
public health mission requires use data
collection activities in collaboration
with multiple local and international
partners. RZB proposes the following
use of pre/posttests to evaluate the
changes in knowledge, attitudes and
practices relating to tick control as well
as perceived impact of the intervention
project. The project will also collect
basic household information to
document their consent to participate.
Data collection will be conducted inperson. Data will be recorded on paper
forms and then entered into an
electronic database.
RZB estimates involvement of 1,300
respondents and a maximum of 600
hours of burden for research activities
each year. The collected information
will not impose a cost burden on the
respondents beyond that associated
with their time to provide the required
data.
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
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.
Proposed Project
Community-based Tick Control for
the Prevention of Rocky Mountain
Spotted Fever in Hermosillo, Mexico’’—
New—National Center for Emerging and
Zoonotic Diseases (NCEZID), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) Rickettsial Zoonoses
Branch (RZB) requests approval of a
public health intervention assessment
tool to demonstrate the efficacy and
impact of public health research related
to the prevention of Rocky Mountain
spotted fever [RMSF] in Hermosillo,
Mexico. These activities include
monitoring cases, conducting tick
control interventions, and performing
participant surveys to assess the
knowledge, attitudes, and practices
relating to tick control and prevention.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Average
burden per
response
(in hours)
Number of
responses per
respondent
Total burden
(in hours)
Type of respondents
Form name
General Public ..................................
General Public ..................................
Registration ......................................
KAP survey (pre and post intervention).
500
800
1
2
20/60
20/60
167
533
Total ...........................................
...........................................................
........................
........................
........................
700
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.
asabaliauskas on DSK5VPTVN1PROD with NOTICES
[FR Doc. 2015–28473 Filed 11–9–15; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–16CQ; Docket No. CDC–2015–
0101]
BILLING CODE 4163–18–P
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
VerDate Sep<11>2014
19:41 Nov 09, 2015
Jkt 238001
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts 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. This notice invites
comment on the ‘‘Occupational Health
Safety Network (OHSN)’’ data
collection.
DATES: Written comments must be
received on or before January 11, 2016.
SUMMARY:
E:\FR\FM\10NON1.SGM
10NON1
]]>Agencies
[Federal Register Volume 80, Number 217 (Tuesday, November 10, 2015)]
[Notices]
[Pages 69680-69681]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-28473]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-16-16CP; Docket No. CDC-2015-0100]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing efforts 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. This notice invites comment on a proposed
information collection request entitled ``Data Collection for
Community-based Tick Control for the Prevention of Rocky Mountain
Spotted Fever in Hermosillo, Mexico.'' This project will be carried out
in collaboration with the Rickettsial Zoonoses Branch, National Center
for Emerging and Zoonotic Infectious Diseases (NCEZID), Centers for
Disease Control and Prevention (CDC) and the University of Sonora
School of Medicine (UNSOM) to assess the efficacy and impact of a
community based tick prevention project.
DATES: Written comments must be received on or before January 11, 2016.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2015-
0100 by any of the following methods:
Federal eRulemaking Portal: Regulation.gov. Follow the
instructions for submitting comments.
Mail: Leroy A. Richardson, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE., MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. All relevant comments received will be posted
without change to Regulations.gov, including any personal information
provided. For access to the docket to read background documents or
comments received, go to Regulations.gov.
Please note: All public comment should be submitted through the
Federal eRulemaking portal (Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact the Information Collection Review Office,
Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS-
D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of
[[Page 69681]]
Management and Budget (OMB) for each collection of information they
conduct or sponsor. In addition, the PRA also requires Federal agencies
to provide a 60-day notice in the Federal Register concerning each
proposed collection of information, including each new proposed
collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
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 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.
Proposed Project
Community-based Tick Control for the Prevention of Rocky Mountain
Spotted Fever in Hermosillo, Mexico''--New--National Center for
Emerging and Zoonotic Diseases (NCEZID), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) Rickettsial
Zoonoses Branch (RZB) requests approval of a public health intervention
assessment tool to demonstrate the efficacy and impact of public health
research related to the prevention of Rocky Mountain spotted fever
[RMSF] in Hermosillo, Mexico. These activities include monitoring
cases, conducting tick control interventions, and performing
participant surveys to assess the knowledge, attitudes, and practices
relating to tick control and prevention.
The information collection for which approval is sought is in
accordance with RZB's mission to reduce morbidity and mortality of
rickettsial diseases and decrease the burden of disease through control
and prevention methods. Authorizing Legislation comes from section 301
of the Public Health Service Act (42 U.S.C. 241).
Approval for a three-year data collection will allow RZB to collect
information related to risk of RMSF to improve and inform prevention
activities. Successful execution of RZB's public health mission
requires use data collection activities in collaboration with multiple
local and international partners. RZB proposes the following use of
pre/posttests to evaluate the changes in knowledge, attitudes and
practices relating to tick control as well as perceived impact of the
intervention project. The project will also collect basic household
information to document their consent to participate. Data collection
will be conducted in-person. Data will be recorded on paper forms and
then entered into an electronic database.
RZB estimates involvement of 1,300 respondents and a maximum of 600
hours of burden for research activities each year. The collected
information will not impose a cost burden on the respondents beyond
that associated with their time to provide the required data.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hours)
respondent hours)
----------------------------------------------------------------------------------------------------------------
General Public................ Registration.... 500 1 20/60 167
General Public................ KAP survey (pre 800 2 20/60 533
and post
intervention).
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 700
----------------------------------------------------------------------------------------------------------------
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. 2015-28473 Filed 11-9-15; 8:45 am]
BILLING CODE 4163-18-P
