Proposed Data Collection Submitted for Public Comment and Recommendations, 43842-43844 [2020-15656]
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Federal Register / Vol. 85, No. 139 / Monday, July 20, 2020 / Notices
https://www.cdc.gov/vaccines/acip/
index.html.
You may submit comments, identified
by Docket No. CDC–2020–0083, by
either of the following methods below.
CDC does not accept comment by email.
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Docket No. CDC–2020–0083,
c/o Attn: August ACIP Meeting, Centers
for Disease Control and Prevention,
1600 Clifton Road NE, MS H24–8,
Atlanta, GA 30329–4027.
Instructions: All submissions received
must include the Agency name and
Docket Number. All relevant comments
received in conformance with the
https://www.regulations.gov suitability
policy will be posted without change to
https://www.regulations.gov, including
any personal information provided. For
access to the docket to read background
documents or comments received, go to
https://www.regulations.gov.
FOR FURTHER INFORMATION CONTACT:
Stephanie Thomas, ACIP Committee
Management Specialist, Centers for
Disease Control and Prevention,
National Center for Immunization and
Respiratory Diseases, 1600 Clifton Road
NE, MS–H24–8, Atlanta, GA 30329–
4027; Telephone: 404–639–8367; Email:
ACIP@cdc.gov.
SUPPLEMENTARY INFORMATION:
Purpose: The committee is charged
with advising the Director, CDC, on the
use of immunizing agents. In addition,
under 42 U.S.C. 1396s, the committee is
mandated to establish and periodically
review and, as appropriate, revise the
list of vaccines for administration to
vaccine-eligible children through the
Vaccines for Children (VFC) program,
along with schedules regarding dosing
interval, dosage, and contraindications
to administration of vaccines. Further,
under provisions of the Affordable Care
Act, section 2713 of the Public Health
Service Act, immunization
recommendations of the ACIP that have
been approved by the Director of the
Centers for Disease Control and
Prevention and appear on CDC
immunization schedules must be
covered by applicable health plans.
Matters to be Considered: The agenda
will include discussions on COVID–19
vaccines. No recommendation votes are
scheduled. Agenda items are subject to
change as priorities dictate. For more
information on the meeting agenda visit
https://www.cdc.gov/vaccines/acip/
meetings/meetings-info.html.
Meeting Information: The meeting
will be webcast live via the World Wide
Web; for more information on ACIP
please visit the ACIP website: https://
www.cdc.gov/vaccines/acip/.
VerDate Sep<11>2014
18:30 Jul 17, 2020
Jkt 250001
Public Participation
Interested persons or organizations
are invited to participate by submitting
written views, recommendations, and
data. Comments received are part of the
public record and are subject to public
disclosure. Do not include any
information in your comment or
supporting materials that you consider
confidential or inappropriate for public
disclosure. If you include your name,
contact information, or other
information that identifies you in the
body of your comments, that
information will be on public display.
CDC will review all submissions and
may choose to redact, or withhold,
submissions containing private or
proprietary information such as Social
Security numbers, medical information,
inappropriate language, or duplicate/
near duplicate examples of a mass-mail
campaign. CDC will carefully consider
all comments submitted into the docket.
CDC does not accept comment by email.
Oral Public Comment: This meeting
will include time for members of the
public to make an oral comment. Oral
public comment will occur before any
scheduled votes including all votes
relevant to the ACIP’s Affordable Care
Act and Vaccines for Children Program
roles. Priority will be given to
individuals who submit a request to
make an oral public comment before the
meeting according to the procedures
below.
Procedure for Oral Public Comment:
All persons interested in making an oral
public comment at the August ACIP
meeting must submit a request at https://
www.cdc.gov/vaccines/acip/meetings/
no later than 11:59 p.m., EDT, August
19, 2020 according to the instructions
provided.
If the number of persons requesting to
speak is greater than can be reasonably
accommodated during the scheduled
time, CDC will conduct a lottery to
determine the speakers for the
scheduled public comment session.
CDC staff will notify individuals
regarding their request to speak by email
by August 20, 2020. To accommodate
the significant interest in participation
in the oral public comment session of
ACIP meetings, each speaker will be
limited to 3 minutes, and each speaker
may only speak once per meeting.
Written Public Comment: Written
comments must be received on or before
August 27, 2020. Written public
comments submitted by 72 hours prior
to the ACIP meeting will be provided to
ACIP members before the meeting.
The Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, Centers for Disease
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Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
[FR Doc. 2020–15614 Filed 7–17–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–20QD; Docket No. CDC–2020–
0076]
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 ‘‘Reducing Fatigue Among Taxi
Drivers’’ with the goal of evaluating two
interventions, a training and a wristdevice that provides personalized daily
fatigue scores, designed to enable taxi
drivers to reduce their fatigue levels.
This research study involves two parts:
Development of a fatigue management
eLearning training tool designed for
drivers-for-hire (e.g., taxi drivers; ride
sourcing drivers); and an evaluation of
the effectiveness of this training alone
and paired with the wrist-device that
provides personalized daily fatigue
scores.
SUMMARY:
CDC must receive written
comments on or before September 18,
2020.
DATES:
You may submit comments,
identified by Docket No. CDC–2020–
0076 by any of the following methods:
ADDRESSES:
E:\FR\FM\20JYN1.SGM
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Federal Register / Vol. 85, No. 139 / Monday, July 20, 2020 / Notices
• 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: 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 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
VerDate Sep<11>2014
18:30 Jul 17, 2020
Jkt 250001
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Reducing Fatigue Among Taxi
Drivers—New—National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Taxi drivers routinely work long
hours and late night or early morning
shifts. Shift work and long work hours
are linked to many health and safety
risks due to disturbances to sleep and
circadian rhythms. Fatigue is a
significant contributor to transportationrelated injuries, most notably among
shift workers. Such work schedules and
inadequate sleep likely contribute to
health issues and injuries among taxi
drivers who experience a roadway
fatality rate of 3.5 times higher than all
civilian workers and had the highest
rate of nonfatal work-related motor
vehicle injuries treated in emergency
departments.
The urban and interurban
transportation industry ranks the third
highest in costs per employee for motor
vehicle crashes. Tired drivers endanger
others on the road (e.g., other drivers,
passengers, bicyclists, pedestrians) in
addition to themselves and their
passengers. An important approach to
reducing fatigue-related risks is to
inform employers and taxi drivers about
the risks and strategies to reduce their
risks.
The purpose of this project is to
develop and evaluate a training program
to inform taxi drivers and other drivers
for hire who transport passengers of the
risks linked to shift work and long work
hours and evaluate strategies for taxi
drivers to reduce these risks. The
proposed study site will be the
Flywheel Taxi Company in San
Francisco, CA with approximately 500
drivers, who have agreed to share data
collected on the study participants. The
recruitment of 180 study participants
and data collection onsite will be
performed by a NIOSH contractor
trained by the NIOSH project personnel.
This research study involves two parts:
Development of a fatigue management
eLearning training tool designed for
drivers-for-hire (e.g., taxi drivers; ride
sourcing drivers); and an evaluation of
the use of this tool as an intervention.
The training tool will educate drivers
about fatigue as a risk factor for motor
vehicle crashes, the negative health and
safety effects of fatigue, and how to
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
43843
reduce fatigue by improving sleep,
health, nutrition and work schedules.
There will be pre- and post-module
knowledge tests to evaluate the training.
The training will be offered online, free
of charge, and will be viewable on
multiple platforms (e.g., smartphone,
tablet, laptop). All participants will also
wear a wristband actigraph used to
measure sleep/wake cycles, which will
serve as a second intervention. The
actigraph data will provide a
personalized daily measure of fatigue
each participant can use as an external
prompt to assess individual fatigue
levels and trigger self-reflection on
fitness to drive and act accordingly. A
randomized pre-post with control group
longitudinal study design will evaluate
the training and the driver’s response to
feedback from the actigraph.
Specifically, there are two intervention
groups: (1) Training plus actigraph
fatigue level feedback and (2) training
only with wearing actigraph but no
fatigue level feedback. The control
group will receive neither training nor
feedback on fatigue levels from their
actigraph. Participants will complete a
baseline and follow-up Work and Health
survey, sleep and activities diaries, and
sleep health knowledge questions
during each of five observation periods.
The Work and Health survey
administered in the first observation
period will be more comprehensive and
the abbreviated follow up Work and
Health surveys administered for the
remaining observation periods will
serve to capture only responses to
questions that can change from one
observation period to the next. Only
participants randomly selected to take
the training will complete a training
evaluation survey used to strengthen the
training’s effectiveness. Data will also be
collected from company installed invehicle monitoring systems on safety
critical events (e.g., hard braking,
speeding) already collected on all
drivers as a direct measurement of
fatigue-related driving performance
events used to validate self-report data.
As part of their daily sleep and health
diaries drivers will be asked to complete
three minute psychomotor vigilance
tests (PVTs) five times throughout the
day to directly measure alertness using
an app installed on an electronic device.
At the end of the data collection period
the training will be offered to the
remaining study participants who will
be provided an opportunity, but no
remuneration, to complete the training
and training survey.
Study staff will use the findings from
this evaluation to improve the training
program, including content and
E:\FR\FM\20JYN1.SGM
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43844
Federal Register / Vol. 85, No. 139 / Monday, July 20, 2020 / Notices
delivery, as well as compare fatigue
between intervention groups. Potential
impacts of this project include
improvements in work behaviors for
coping with shift work and long work
hours and an objective reduction in
fatigue compared to the control groups.
This project is poised to have
considerable impact in the contribution
of an evidence base for effective
interventions that could be used by
participant will complete the sleep and
activity diary five times a day, each day
for 35 days (175 times total) which will
require approximately two minutes for
each response. There will also be three
meetings for recruitment and enrollment
(once), fitting the actigraph (weekly),
and a final meeting. The total estimated
annualized burden hours is 2,700. There
are no costs to participants other than
their time.
other taxi companies and drivers for
ride sourcing companies to promote
strategies in road safety.
The burden table lists 120 of the 180
taxi drivers in the study will complete
the online training and evaluation
(approximately three hours). All drivers
(180) will complete the Work and
Health survey, and the knowledge
survey each week of the study (five
times each per participant). Each
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hours)
Total burden
(in hours)
Type of respondents
Form name
Taxi Drivers .......................................
Online Training & Evaluation ...........
Sleep & Activities Diary ....................
Work & Health Survey .....................
Knowledge survey ............................
Recruitment & Informed Consent ....
Initial Meeting (Fit Actigraph) ...........
10-minute meeting (turn in devices,
turn in diary, receive remuneration).
120
180
180
180
180
180
180
1
175
5
5
1
5
5
3
2/60
45/60
15/60
30/60
10/60
10/60
360
1,050
675
225
90
150
150
Total ...........................................
...........................................................
........................
........................
........................
2,700
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–15656 Filed 7–17–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–0576]
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 Possession, Use,
and Transfer of Select Agents and
Toxins 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 April 3, 2020 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
VerDate Sep<11>2014
18:30 Jul 17, 2020
Jkt 250001
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
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
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
Possession, Use, and Transfer of
Select Agents and Toxins (OMB Control
No. 0920–0576, Exp. 10/31/2020)—
Revision—Center for Preparedness and
Response (CPR), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Subtitle A of the Public Health
Security and Bioterrorism Preparedness
and Response Act of 2002, (42 U.S.C.
262a), requires the United States
Department of Health and Human
Services (HHS) to regulate the
possession, use, and transfer of
biological agents or toxins that have the
potential to pose a severe threat to
public health and safety (select agents
and toxins). Subtitle B of the Public
Health Security and Bioterrorism
Preparedness and Response Act of 2002
(which may be cited as the Agricultural
Bioterrorism Protection Act of 2002), (7
U.S.C. 8401), requires the United States
Department of Agriculture (USDA) to
regulate the possession, use, and
E:\FR\FM\20JYN1.SGM
20JYN1
]]>Agencies
[Federal Register Volume 85, Number 139 (Monday, July 20, 2020)]
[Notices]
[Pages 43842-43844]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-15656]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-20-20QD; Docket No. CDC-2020-0076]
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 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 ``Reducing Fatigue Among Taxi
Drivers'' with the goal of evaluating two interventions, a training and
a wrist-device that provides personalized daily fatigue scores,
designed to enable taxi drivers to reduce their fatigue levels. This
research study involves two parts: Development of a fatigue management
eLearning training tool designed for drivers-for-hire (e.g., taxi
drivers; ride sourcing drivers); and an evaluation of the effectiveness
of this training alone and paired with the wrist-device that provides
personalized daily fatigue scores.
DATES: CDC must receive written comments on or before September 18,
2020.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2020-
0076 by any of the following methods:
[[Page 43843]]
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
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
Reducing Fatigue Among Taxi Drivers--New--National Institute for
Occupational Safety and Health (NIOSH), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Taxi drivers routinely work long hours and late night or early
morning shifts. Shift work and long work hours are linked to many
health and safety risks due to disturbances to sleep and circadian
rhythms. Fatigue is a significant contributor to transportation-related
injuries, most notably among shift workers. Such work schedules and
inadequate sleep likely contribute to health issues and injuries among
taxi drivers who experience a roadway fatality rate of 3.5 times higher
than all civilian workers and had the highest rate of nonfatal work-
related motor vehicle injuries treated in emergency departments.
The urban and interurban transportation industry ranks the third
highest in costs per employee for motor vehicle crashes. Tired drivers
endanger others on the road (e.g., other drivers, passengers,
bicyclists, pedestrians) in addition to themselves and their
passengers. An important approach to reducing fatigue-related risks is
to inform employers and taxi drivers about the risks and strategies to
reduce their risks.
The purpose of this project is to develop and evaluate a training
program to inform taxi drivers and other drivers for hire who transport
passengers of the risks linked to shift work and long work hours and
evaluate strategies for taxi drivers to reduce these risks. The
proposed study site will be the Flywheel Taxi Company in San Francisco,
CA with approximately 500 drivers, who have agreed to share data
collected on the study participants. The recruitment of 180 study
participants and data collection onsite will be performed by a NIOSH
contractor trained by the NIOSH project personnel. This research study
involves two parts: Development of a fatigue management eLearning
training tool designed for drivers-for-hire (e.g., taxi drivers; ride
sourcing drivers); and an evaluation of the use of this tool as an
intervention. The training tool will educate drivers about fatigue as a
risk factor for motor vehicle crashes, the negative health and safety
effects of fatigue, and how to reduce fatigue by improving sleep,
health, nutrition and work schedules. There will be pre- and post-
module knowledge tests to evaluate the training. The training will be
offered online, free of charge, and will be viewable on multiple
platforms (e.g., smartphone, tablet, laptop). All participants will
also wear a wristband actigraph used to measure sleep/wake cycles,
which will serve as a second intervention. The actigraph data will
provide a personalized daily measure of fatigue each participant can
use as an external prompt to assess individual fatigue levels and
trigger self-reflection on fitness to drive and act accordingly. A
randomized pre-post with control group longitudinal study design will
evaluate the training and the driver's response to feedback from the
actigraph. Specifically, there are two intervention groups: (1)
Training plus actigraph fatigue level feedback and (2) training only
with wearing actigraph but no fatigue level feedback. The control group
will receive neither training nor feedback on fatigue levels from their
actigraph. Participants will complete a baseline and follow-up Work and
Health survey, sleep and activities diaries, and sleep health knowledge
questions during each of five observation periods. The Work and Health
survey administered in the first observation period will be more
comprehensive and the abbreviated follow up Work and Health surveys
administered for the remaining observation periods will serve to
capture only responses to questions that can change from one
observation period to the next. Only participants randomly selected to
take the training will complete a training evaluation survey used to
strengthen the training's effectiveness. Data will also be collected
from company installed in-vehicle monitoring systems on safety critical
events (e.g., hard braking, speeding) already collected on all drivers
as a direct measurement of fatigue-related driving performance events
used to validate self-report data. As part of their daily sleep and
health diaries drivers will be asked to complete three minute
psychomotor vigilance tests (PVTs) five times throughout the day to
directly measure alertness using an app installed on an electronic
device. At the end of the data collection period the training will be
offered to the remaining study participants who will be provided an
opportunity, but no remuneration, to complete the training and training
survey.
Study staff will use the findings from this evaluation to improve
the training program, including content and
[[Page 43844]]
delivery, as well as compare fatigue between intervention groups.
Potential impacts of this project include improvements in work
behaviors for coping with shift work and long work hours and an
objective reduction in fatigue compared to the control groups. This
project is poised to have considerable impact in the contribution of an
evidence base for effective interventions that could be used by other
taxi companies and drivers for ride sourcing companies to promote
strategies in road safety.
The burden table lists 120 of the 180 taxi drivers in the study
will complete the online training and evaluation (approximately three
hours). All drivers (180) will complete the Work and Health survey, and
the knowledge survey each week of the study (five times each per
participant). Each participant will complete the sleep and activity
diary five times a day, each day for 35 days (175 times total) which
will require approximately two minutes for each response. There will
also be three meetings for recruitment and enrollment (once), fitting
the actigraph (weekly), and a final meeting. The total estimated
annualized burden hours is 2,700. There are no costs to participants
other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
Taxi Drivers.................. Online Training 120 1 3 360
& Evaluation.
Sleep & 180 175 2/60 1,050
Activities
Diary.
Work & Health 180 5 45/60 675
Survey.
Knowledge survey 180 5 15/60 225
Recruitment & 180 1 30/60 90
Informed
Consent.
Initial Meeting 180 5 10/60 150
(Fit Actigraph).
10-minute 180 5 10/60 150
meeting (turn
in devices,
turn in diary,
receive
remuneration).
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 2,700
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-15656 Filed 7-17-20; 8:45 am]
BILLING CODE 4163-18-P
