60 Day FRN

59381

Federal Register / Vol. 84, No. 213 / Monday, November 4, 2019 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)

Number of
responses per
respondent

Number of
respondents

Total burden
(in hours)

Type of respondent

Form name

Airline Medical Officer or Equivalent/
Computer and Information Systems Manager.
Airline Medical Officer or Equivalent/
Computer and Information Systems Manager.
Traveler .............................................

Domestic TB Manifest Template or
Informal Manifest Request.

2

1

360/60

12

Domestic Non-TB Manifest Template or Informal Manifest Request.
Public Health Passenger Locator
Form: Outbreak of public health
significance* (international flights).
Public Health Passenger Locator
Form: Limited onboard exposure †
(international flights).
Public Health Passenger Locator
Form (domestic flights).

48

1

360/60

288

2,700,000

1

5/60

225,000

800

1

5/60

67

800

1

5/60

67

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

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

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

225,434

Traveler .............................................
Traveler .............................................
Total ...........................................

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

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–24006 Filed 11–1–19; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–0995; Docket No. CDC–2019–
0097]

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 effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled National Network of Sexually
Transmitted Diseases Clinical
Prevention Training Centers.’’ The
purpose of the collection is to support
program management of the National
Network of Sexually Transmitted
Disease Clinical Prevention Training
Center (NNPTC) and to evaluate the

SUMMARY:

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reach and impact of the NNPTC’s
training activities.
DATES: CDC must receive written
comments on or before January 3, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2019–
0097 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
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 Jeffrey M. Zirger,
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
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

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proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. 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 submissions
of responses.
5. Assess information collection costs.
Proposed Project
National Network of Sexually
Transmitted Diseases Clinical
Prevention Training Centers (NNPTC):
Evaluation (OMB Control No. 0920–
0995, Exp. 05/31/2020)—Extension—
National Center for HIV/AIDS, Viral
Hepatitis, STD, and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).

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59382

Federal Register / Vol. 84, No. 213 / Monday, November 4, 2019 / Notices

Background and Brief Description
The Centers for Disease Control and
Prevention (CDC), Division of STD
Prevention requests an extension and
three-year approval of the currently
approved information collection request
that comprises the NNPTC Abbreviated
Health Professional Application for
Training (NNPTC Abbreviated HPAT).
This extension will allow the NNPTC
Abbreviated HPAT to continue to serve
as the official training application form
used for training activities conducted by
the Sexually Transmitted Disease (STD)
Prevention Training Centers’ (PTCs)
grantees funded by the (CDC).
The PTCs are funded by CDC/Division
of STD Prevention (DSTDP) to provide
training and capacity-building that
includes information, training, technical
assistance and technology transfer. PTCs
offer classroom and experiential
training, web-based training, clinical
consultation, and capacity building
assistance to maintain and enhance the
capacity of health care professionals to
control and prevent STDs and HIV. The
NNPTC Abbreviated HPAT is used to
monitor and evaluate performance and
reach of grantees that offer STD and HIV
prevention training, training assistance,
and capacity building assistance to
physicians, nurses, disease intervention

specialists, and health educators. During
the previously approved three-year
period, data was collected to monitor
and evaluate the performance of the
NNPTC grantees and the NNPTC
program. This data provided the NNPTC
with necessary information to improve
program processes and operations in
order to improve the quality of STD
prevention and treatment.
The 4,500 respondents (who will
engage in a total of 11,769 respondent
instances) represent an average of the
number of health professionals trained
by PTC grantees during 2015. The
evaluation instruments collect data on
the impact of the training by the
NNPTC. This data collection is
necessary to assess and evaluate the
performance of the grantees in
delivering training and to standardize
training registration processes across the
PTCs. The NNPTC Abbreviated HPAT
allows CDC grantees to use a single
instrument when collecting
demographic data from its training and
capacity building participants, regarding
their: (1) Occupations, professions, and
functional roles; (2) principal
employment settings; (3) location of
their work settings; and (4)
programmatic and population foci of
their work. The NNPTC Abbreviated
HPAT takes approximately three

minutes to complete. This data
collection provides CDC with
information to determine whether the
training grantees are reaching their
target audiences in terms of provider
type, the types of organizations in
which participants work, the focus of
their work and the population groups
and geographic areas served.
The evaluation instruments are used
to assess training and capacity-building
outcomes (knowledge, confidence,
intention to use information, actual
changes made as a result of training)
immediately after, and again 90 days
after training events. The evaluation
instruments vary based on the type of
training offered and take between
approximately 16 minutes (for intensive
multi-day trainings) to two minutes to
complete (for short didactic or webinar
sessions).
The CDC’s Funding Opportunity
Announcement PS 14–1407, National
Network of Sexually Transmitted
Diseases Clinical Prevention Training
Centers (NNPTC) requires the collection
of national demographic information on
grantees’ trainees and national
evaluation outcomes. There are no costs
to respondents other than their time.
The estimated annualized burden hours
for this data collection are 502 hours.

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Average
burden per
response
(in hours)

Number
responses per
respondent

Total burden
hours

Type of respondent

Form name

Healthcare Professionals .........

4,500

1

3/60

225

116

1

16/60

31

36
166
58
70
20
40
15
548

1
1
1
1
1
1
1
1

10/60
10/60
7/60
4/60
3/60
3/60
2/60
6/60

6
28
7
5
1
2
1
55

180

1

5/60

15

Healthcare Professionals .........
Healthcare Professionals .........

NNPTC Abbreviated Health Professional
Application for Training (HPAT).
Intensive Complete Post-Course Evaluation.
Intensive CompleteLong-TermEvaluation
Intensive-DidacticPost-CourseEvaluation
Intensive-DidacticLong-TermEvaluation ...
PracticumPost-CourseEvaluation .............
PracticumLong-TermEvaluation ................
Wet MountPost-CourseEvaluation ............
Wet MountLong-TermEvaluation ..............
STD Tx Guidelines Complete PostCourseEvaluation.
STD Tx Guidelines Complete LongTermEvaluation.
Short GuidelinesPost-CourseEvaluation ..
Short GuidelinesLong-Term Evaluation ....
BasicPost-CourseEvaluation ....................
BasicLong-Term Evaluation ......................
Immediate Post-Course email invitation ...
3 Month Long-Term email invitation .........

500
160
150
50
4,500
660

1
1
1
1
1
1

3/60
3/60
2/60
2/60
1/60
1/60

25
8
5
2
75
11

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

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

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

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

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

502

Healthcare Professionals .........
Healthcare Professionals .........
Healthcare Professionals .........
Healthcare Professionals .........
Healthcare Professionals .........

Healthcare Professionals .........
Healthcare Professionals .........

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Federal Register / Vol. 84, No. 213 / Monday, November 4, 2019 / Notices
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–24005 Filed 11–1–19; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–20–20AZ; Docket No. CDC–2019–
0099]

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 effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Evaluation of the Effectiveness of
the Training and Education Modules in
the North American Fatigue
Management Program, which is an
observational study evaluating 180 longhaul and regional truck drivers in a
naturalistic driving study over eight
months. Questionnaires, in-vehicle
monitor system, Actigraphy devices,
and smartphones will be used in the
data collection.
DATES: CDC must receive written
comments on or before January 3, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2019–
0099 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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. CDC will post, without
change, all relevant comments to
Regulations.gov.
SUMMARY:

Please note: Submit all comments through
the Federal eRulemaking portal

VerDate Sep<11>2014

20:48 Nov 01, 2019

Jkt 250001

(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 Jeffrey M. Zirger,
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
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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. 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 submissions
of responses.
5. Assess information collection costs.
FOR FURTHER INFORMATION CONTACT:

Proposed Project
Evaluation of the Effectiveness of the
Training and Education Modules in the
North American Fatigue Management
Program—New—National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).

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59383

Background and Brief Description
The mission of the National Institute
for Occupational Safety and Health
(NIOSH) is to promote safety and health
at work for all people through research
and prevention. Reducing fatiguerelated crashes is one of the top 10
changes needed to reduce transportation
accidents and save lives identified by
the National Transportation Safety
Board (NTSB) for 2017–2018 and a
National Occupational Research Agenda
(NORA) priority.
Fatigue is a preventable cause of
crashes. The North American Fatigue
Management Program (NAFMP) was
developed by the Federal Motor Carrier
Safety Administration, Transport
Canada, and other entities to address
commercial motor vehicle (CMV) driver
fatigue through a comprehensive
approach that delivers prevention
information to carriers, dispatchers,
drivers, and family members. In 2015,
the National Academy of Sciences
published the report ‘‘Commercial
motor vehicle driver fatigue, long-term
health, and highway safety research
needs’’ that identified the need for fully
evaluating the NAFMP so that
recommendations for implementation of
NAFMP are supported by scientific
evidence. NIOSH is collaborating with
the FMCSA to ensure the success of the
proposed study.
Data will be collected from CMV
drivers (hereafter referred to as ‘‘driver’’)
during their application to participate in
the study, briefing session, study
participation, and debriefing session.
Data collection will primarily focus on
driving performance, sleep, and
sleepiness. These outcomes will be
compared between pre-rollout of the
NAFMP (in which drivers will operate
as they did before their participation in
the study) and after the rollout of the
NAFMP training and education modules
(in which drivers and managers will
operate with increased knowledge,
strategies, and techniques to reduce
their fatigue). All drivers interested in
participating in the study may complete
the application. A briefing session will
be scheduled with drivers who are
found eligible for the study. During the
briefing session, drivers who provide
informed consent will be enrolled in the
study. Drivers will have a debriefing
session if a driver chooses to withdraw
from the study early or upon completion
of the eight-month participation period.
The sample of drivers in the study
will include those employed as drivers
at the participating carriers. Drivers who
have a valid Class-A commercial
driver’s license (CDL) and work at the
participating company in regional and

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