Agency Forms Undergoing Paperwork Reduction Act Review, 53380-53381 [2020-18994]
Download as PDF
<![CDATA[
53380
Federal Register / Vol. 85, No. 168 / Friday, August 28, 2020 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
State Administrators ........................................
District Administrators .....................................
School Administrators .....................................
Teachers .........................................................
Students ..........................................................
State-level Recruitment Script for the NYTS
District-level Recruitment Script for the NYTS
School-level Recruitment Script for the NYTS
Data Collection Checklist ...............................
National Youth Tobacco Survey ....................
Cognitive Testing ...........................................
Survey Pre-tests .............................................
Testing Activities ............................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–18995 Filed 8–27–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–20AZ]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Evaluation of
the Effectiveness of the Training and
Education Modules in the North
American Fatigue Management Program
to the Office of Management and Budget
(OMB) for review and approval. CDC
previously published a ‘‘Proposed Data
Collection Submitted for Public
Comment and Recommendations’’
notice on November 4, 2019 to obtain
comments from the public and affected
agencies. CDC received one comment
related to the previous notice. This
notice serves to allow an additional 30
days for public and affected agency
comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(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,
VerDate Sep<11>2014
17:16 Aug 27, 2020
Jkt 250001
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.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
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)
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 fatigue-
PO 00000
Frm 00064
Fmt 4703
Sfmt 4703
33
253
281
1,177
24,000
40
30
300
Number of
responses per
respondent
1
1
1
1
1
1
1
1
Average
burden per
response
(in hr.)
30/60
30/60
30/60
15/60
45/60
120/60
45/60
10/60
related crashes is one of the top 10
changes needed to reduce transportation
accidents and save lives identified by
the National Transportation Safety
Board (NTSB) 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 FMCSA, 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.
NIOSH will recruit two commercial
vehicle carriers, and CMV drivers,
hereafter referred to as ‘‘drivers’’,
employed by those carriers. Data will be
collected during drivers’ 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
E:\FR\FM\28AUN1.SGM
28AUN1
53381
Federal Register / Vol. 85, No. 168 / Friday, August 28, 2020 / Notices
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 8month participation period.
Drivers who have a valid Class-A
commercial driver’s license (CDL) and
work at the participating company in
regional and long-haul operations for at
least one year will be eligible for the
study. A convenience sample of 180
eligible drivers will be recruited to
participate in the study. The study
sample will include approximately 90
regional and 90 long-haul drivers. There
will be no required minimum number of
female or minority drivers.
Data will be collected during each
phase: (1) In the application, drivers
will be asked to provide their name and
contact information (home address,
telephone number, and email address)
to allow contact from the research team
regarding their eligibility for the study.
(2) In the briefing session, drivers will
be asked to complete the Background
Questionnaire. (3) During the study,
information collection will occur
through several streams: (a) A real-time
fatigue monitoring system installed in
the participating driver’s vehicle; (b)
Smart phone apps to collect data from
a psychomotor vigilance test, the
Karolinska Sleepiness Scale, a sleep log,
a difficulty of drive scale, a degree of
drive hazards scale, a fatigue scale, and
a stress scale; (c) an electronic logging
device which will record information
about the driver’s hours of service and
driving; (d) a wrist actigraphy device to
collect data on driver sleep and wake
times. Drivers will be asked to
synchronize the actigraph with a
smartphone app daily; (e) smartphone
or web-based questionnaires including
an Exercise and Food Consumption
Questionnaire, the quality of life short
form 36 version-2 questionnaire (SF–
36v2), Family Interactions
Questionnaire, and Job Descriptive
Index. These will be completed by
drivers at four different intervals,
including the beginning (1st week) and
middle (2nd month) of the baseline
phase, and the middle (5th month) and
end (8th month) of the intervention
phase; (f) A questionnaire to assess
corporate practices and corporate safety
climate will be given to managers at the
participating carriers. These will be
completed by managers at the beginning
(1st week) of the study and end (8th
month) of the intervention phase; and
(g) During the field study, carriers will
be asked to provide information
concerning crashes and roadside
violations occurring during each
driver’s period of study participation.
Administrative cost information (e.g.,
equipment, labor, etc.) will also be
collected from the carrier to evaluate
cost-benefit of the intervention.
OMB approval is requested for two
years. Participation is voluntary and
there are no costs to respondents other
than their time. The total estimated
annualized burden is 5,278 hours.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Carrier Management .......................................
Participation Agreement .................................
Retrieval of Company Monthly Roadside Violations/Crash Reports.
Retrieval of Company Administrative Costs ..
Management Practice questionnaire (Time 1)
Management Practice questionnaire (Time 2)
Application to Participate ...............................
Actigraph Training ..........................................
Background Questionnaire .............................
Daily Smartphone Questions .........................
PVT ................................................................
Exercise and Food Consumption Questionnaire.
SF–36v2 .........................................................
Family Interactions Questionnaire .................
Safety Climate Questionnaire ........................
Job Descriptive Index .....................................
Post-Study Questionnaire ..............................
Phone Briefings ..............................................
Drivers .............................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–18994 Filed 8–27–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Screening Tool for Unaccompanied
Alien Children Program Staff and
Visitors (New Collection)
Office of Refugee Resettlement,
Administration for Children and
Families, Health and Human Services
(HHS).
ACTION: Request for public comment.
AGENCY:
VerDate Sep<11>2014
17:16 Aug 27, 2020
Jkt 250001
PO 00000
Frm 00065
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Number of
respondents
Type of respondent
Average
burden per
response
(in hours)
1
1
1
8
1
90/60
1
5
5
150
90
90
90
90
90
16
1
1
1
1
1
720
720
4
2
45/60
45/60
12/60
10/60
45/60
1/60
3/60
20/60
90
90
90
90
90
90
4
4
4
4
1
8
30/60
15/60
10/60
30/60
1
6/60
The Office of Refugee
Resettlement (ORR), Administration for
Children and Families (ACF), U.S.
Department of Health and Human
Services (HHS), is proposing to continue
use of a coronavirus (COVID–19)
screening form for Unaccompanied
Alien Children (UAC) program staff and
visitors at ORR-funded programs. The
form was originally approved under
emergency approval for 6 months. ACF
is requesting a 3-year extension of this
information collection.
DATES: Comments due within 30 days of
publication. OMB is required to make a
decision concerning the collection of
SUMMARY:
E:\FR\FM\28AUN1.SGM
28AUN1
]]>Agencies
[Federal Register Volume 85, Number 168 (Friday, August 28, 2020)]
[Notices]
[Pages 53380-53381]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-18994]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-20-20AZ]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled Evaluation of the Effectiveness of the
Training and Education Modules in the North American Fatigue Management
Program to the Office of Management and Budget (OMB) for review and
approval. CDC previously published a ``Proposed Data Collection
Submitted for Public Comment and Recommendations'' notice on November
4, 2019 to obtain comments from the public and affected agencies. CDC
received one comment related to the previous notice. This notice serves
to allow an additional 30 days for public and affected agency comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(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. Comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. Direct
written comments and/or suggestions regarding the items contained in
this notice to the Attention: CDC Desk Officer, Office of Management
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202)
395-5806. Provide written comments within 30 days of notice
publication.
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)
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 fatigue-related crashes is
one of the top 10 changes needed to reduce transportation accidents and
save lives identified by the National Transportation Safety Board
(NTSB) 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 FMCSA, 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.
NIOSH will recruit two commercial vehicle carriers, and CMV
drivers, hereafter referred to as ``drivers'', employed by those
carriers. Data will be collected during drivers' 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
[[Page 53381]]
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 8-month participation period.
Drivers who have a valid Class-A commercial driver's license (CDL)
and work at the participating company in regional and long-haul
operations for at least one year will be eligible for the study. A
convenience sample of 180 eligible drivers will be recruited to
participate in the study. The study sample will include approximately
90 regional and 90 long-haul drivers. There will be no required minimum
number of female or minority drivers.
Data will be collected during each phase: (1) In the application,
drivers will be asked to provide their name and contact information
(home address, telephone number, and email address) to allow contact
from the research team regarding their eligibility for the study. (2)
In the briefing session, drivers will be asked to complete the
Background Questionnaire. (3) During the study, information collection
will occur through several streams: (a) A real-time fatigue monitoring
system installed in the participating driver's vehicle; (b) Smart phone
apps to collect data from a psychomotor vigilance test, the Karolinska
Sleepiness Scale, a sleep log, a difficulty of drive scale, a degree of
drive hazards scale, a fatigue scale, and a stress scale; (c) an
electronic logging device which will record information about the
driver's hours of service and driving; (d) a wrist actigraphy device to
collect data on driver sleep and wake times. Drivers will be asked to
synchronize the actigraph with a smartphone app daily; (e) smartphone
or web-based questionnaires including an Exercise and Food Consumption
Questionnaire, the quality of life short form 36 version-2
questionnaire (SF-36v2), Family Interactions Questionnaire, and Job
Descriptive Index. These will be completed by drivers at four different
intervals, including the beginning (1st week) and middle (2nd month) of
the baseline phase, and the middle (5th month) and end (8th month) of
the intervention phase; (f) A questionnaire to assess corporate
practices and corporate safety climate will be given to managers at the
participating carriers. These will be completed by managers at the
beginning (1st week) of the study and end (8th month) of the
intervention phase; and (g) During the field study, carriers will be
asked to provide information concerning crashes and roadside violations
occurring during each driver's period of study participation.
Administrative cost information (e.g., equipment, labor, etc.) will
also be collected from the carrier to evaluate cost-benefit of the
intervention.
OMB approval is requested for two years. Participation is voluntary
and there are no costs to respondents other than their time. The total
estimated annualized burden is 5,278 hours.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Carrier Management.................... Participation Agreement. 1 1 1
Retrieval of Company 1 8 90/60
Monthly Roadside
Violations/Crash
Reports.
Retrieval of Company 1 16 2
Administrative Costs.
Management Practice 5 1 45/60
questionnaire (Time 1).
Management Practice 5 1 45/60
questionnaire (Time 2).
Drivers............................... Application to 150 1 12/60
Participate.
Actigraph Training...... 90 1 10/60
Background Questionnaire 90 1 45/60
Daily Smartphone 90 720 1/60
Questions.
PVT..................... 90 720 3/60
Exercise and Food 90 4 20/60
Consumption
Questionnaire.
SF-36v2................. 90 4 30/60
Family Interactions 90 4 15/60
Questionnaire.
Safety Climate 90 4 10/60
Questionnaire.
Job Descriptive Index... 90 4 30/60
Post-Study Questionnaire 90 1 1
Phone Briefings......... 90 8 6/60
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-18994 Filed 8-27-20; 8:45 am]
BILLING CODE 4163-18-P
