Att B_Published 60d FRN

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:

E:\FR\FM\10NON1.SGM

10NON1

69682

Federal Register / Vol. 80, No. 217 / Tuesday, November 10, 2015 / Notices

You may submit comments,
identified by Docket No. CDC–2015–
0101 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.

ADDRESSES:

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 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

asabaliauskas on DSK5VPTVN1PROD with NOTICES

FOR FURTHER INFORMATION CONTACT:

VerDate Sep<11>2014

19:41 Nov 09, 2015

Jkt 238001

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
Occupational Health Safety Network
(OHSN)—Existing Information
Collection in use Without an OMB
Control Number—National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Healthcare in the United States is a
growing industry that employs more
than 19 million workers with a
substantial burden of occupational
injuries and illnesses. In 2013, one in
five workers in the healthcare and social
assistance industry reported a nonfatal
job-related injury. This is the highest
number of non-fatal injuries reported
among all private industries.
U.S. healthcare facilities depend on
surveillance data to track the incidence
of injuries, identify risk factors, target
prevention activities and evaluate
interventions to reduce the occurrence
of occupational injury among healthcare
personnel. To assist healthcare facilities
to enhance capacity to use existing
surveillance data, in 2012, the National
Institute for Occupational Safety and
Health (NIOSH) launched the
Occupational Health Safety Network
(OHSN), a voluntary surveillance
system developed specifically for
healthcare personnel environment.
OHSN is a free and secure electronic
occupational safety and health
surveillance system that has provided
U.S. healthcare facilities the ability to
efficiently analyze their own
occupational injury data while, at the
same time, serving as a source for
national surveillance by sharing their
de-identified injury data with NIOSH.

PO 00000

Frm 00051

Fmt 4703

Sfmt 4703

Unlike other national occupational
surveillance systems, OHSN offers an
integrated approach to monitor standard
occupational injuries among facilitybased healthcare personnel in the U.S.
and to provide timely, facility-level
feedback to participants with
benchmarking and analyses capabilities.
OHSN collects two types of data from
participating facilities. Facilities collect
these data to meet specific regulatory or
administrative requirements. Thus, no
new data collection is required.
Participating facilities provide OHSN a
onetime enrollment. The enrollment
form requests information about the
participating facility, which is
publically available from American
Hospital Association. Participating
facilities also provide a monthly
submission of occupational injury data
collected in the previous month. These
data are sent to OHSN via a web portal
in a format using standardized data
elements and value sets. No personal
identifiable information is transmitted
to OHSN. Data elements include: Injury
time, location and surrounding
circumstances of each injury event.
Healthcare facilities download data
through an OHSN-provided data
conversion and mapping tools which
uploads the monthly occupational
injury data.
Each participating facility has access
to the OHSN web portal, facilities are
able to analyze current and historical
data to benchmark their worker injury
rates and trends and compare their data
to aggregate data from similar
workplaces. In addition they are able to
assess the impact of prevention efforts
on occupational health and safety over
time using aggregated data analysis and
visualization tools (charts and graphs).
OHSN currently tracks three common,
serious, and preventable categories of
traumatic injury to healthcare
personnel: Slips, trips and falls;
musculoskeletal disorders resulting
from patient handling and movement
events; and workplace violence. NIOSH
proposes to add new modules about
exposure to sharps injury and blood and
body fluids exposures.
NIOSH analyzes the data submitted to
OHSN to conduct occupational health
surveillance and to produce periodic
aggregate reports on the occurrence of
and risk factors for occupational injuries
among all OHSN facilities.
OHSN has been operating
continuously and receiving voluntary
monthly reports from 116 participating
facilities since 2012 and is projected to
enroll total of 300 facilities in the next
3 years. NIOSH seeks approval for an
OMB control number to continue this

E:\FR\FM\10NON1.SGM

10NON1

69683

Federal Register / Vol. 80, No. 217 / Tuesday, November 10, 2015 / Notices
important work. There is no cost to the
respondents other than their time.

ESTIMATED ANNUALIZED BURDEN HOURS
Total burden
(in hrs.)

Form name

U.S. healthcare facilities ...................

300

12

3/60

180

U.S. healthcare facilities ...................

Occupational Health Safety Network
(OHSN).
Enrollment form ................................

300

1

1/60

5

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

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

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

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

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

185

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. 2015–28474 Filed 11–9–15; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

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.

Centers for Disease Control and
Prevention

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.

[60Day–16–16CM; Docket No. CDC–2015–
0097]

FOR FURTHER INFORMATION CONTACT:

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:

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. CDC is requesting a new
three-year approval for ‘‘The
Cooperative Re-engagement Controlled
Trial (CoRECT)’’ information
collections.

SUMMARY:

Written comments must be
received on or before January 11, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0097 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
DATES:

asabaliauskas on DSK5VPTVN1PROD with NOTICES

Average
burden per
response
(in hrs.)

Number of
responses per
respondent

Number of
respondents

Type of respondents

VerDate Sep<11>2014

19:41 Nov 09, 2015

Jkt 238001

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
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

PO 00000

Frm 00052

Fmt 4703

Sfmt 4703

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
The Cooperative Re-engagement
Controlled Trial (CoRECT)—New—
National Center for HIV/AIDS, Viral
Hepatitis, STD, and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC), National Center for
HIV/AIDS, Viral Hepatitis, STD, and TB
Prevention (NCHHSTP), Division of
HIV/AIDS Prevention (DHAP) requests a
new three-year OMB approval for
information collection for a new
research study entitled ‘‘The
Cooperative Re-engagement Controlled
Trial (CoRECT)’’. The purpose of the
study is to evaluate a combined health
department and clinic intervention to
improve engagement in HIV care.

E:\FR\FM\10NON1.SGM

10NON1