60 Day FRN - published

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

Women with SLE diagnosis.
Men with SLE diagnosis

Total .......................

Total burden
(in hrs.)

192

1

10/60

32

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

..............................................................................

........................

........................

........................

606

[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.
AGENCY:
asabaliauskas on DSK5VPTVN1PROD with NOTICES

Average
burden per
response
(in hrs.)

Number of
responses per
respondent

Screener ...............................................................

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.

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

Number of
respondents

Form name

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

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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: [email protected].
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:

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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
Average
burden per
response
(in hours)

Number of
responses per
respondent

Total burden
(in hours)

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.
[FR Doc. 2015–28473 Filed 11–9–15; 8:45 am]
asabaliauskas on DSK5VPTVN1PROD with NOTICES

Number of
respondents

Type of respondents

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:

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