Att 2_FRN (60dy) published

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set forth in the 2018 renewal of OMB
Collection No. 3060–0392 will change.
The Commission will use the
information collected under this
revision to 47 CFR 1.1413 to hear and
resolve pole access complaints brought
by ILECs and to determine the merits of
the complaints.
Federal Communications Commission.
Katura Jackson,
Federal Register Liaison Officer, Office of the
Secretary.
[FR Doc. 2018–26411 Filed 12–4–18; 8:45 am]
BILLING CODE 6712–01–P

FEDERAL ELECTION COMMISSION
Sunshine Act Meeting
FEDERAL REGISTER CITATION NOTICE OF
PREVIOUS ANNOUNCEMENT: 83 FR 62320.
PREVIOUSLY ANNOUNCED TIME AND DATE OF
THE MEETING: Wednesday, December 5,

2018 at 2:00 p.m. and continued on
Thursday, December 6, 2018 after the
open meeting.
CHANGES IN THE MEETING: The meeting
will only take place on Thursday,
December 6, 2018 following the open
meeting.
*
*
*
*
*
CONTACT FOR MORE INFORMATION: Judith
Ingram, Press Officer, Telephone: (202)
694–1220.
Laura E. Sinram,
Deputy Secretary of the Commission.

that seek to request a transportation
delegation of authority in the future
must contact GSA–OGP Office of Asset
and Transportation Management for
instructions on how to make this
request.
DATES:

December 5, 2018.

For
clarification of content or information
regarding a request for a delegation of
authority, please contact Mr. Ron Siegel,
Office of Government-wide Policy,
Office of Asset and Transportation
Management, at 202–702–0840, or by
email at gsa-ogp-transportationpolicy@
gsa.gov. Please cite Notice for Rescission
of FMR Bulletin D–1 in the subject line.
SUPPLEMENTARY INFORMATION: Executive
Order 13777, Enforcing the Regulatory
Reform Agenda, Section 3, paragraph
(d)(ii), states in part, the Regulatory
Reform Task Force shall attempt to
identify regulations that are outdated,
unnecessary, or ineffective. Upon
review, GSA has identified GSA
Bulletin FMR D–1, Transportation
Management, as unduly prescriptive
and ineffective. Furthermore, the
bulletin potentially impacts the category
management strategy for procurement.
FOR FURTHER INFORMATION CONTACT:

Dated: November 29, 2018.
Jessica Salmoiraghi,
Associate Administrator, Office of
Government-wide Policy.
[FR Doc. 2018–26409 Filed 12–4–18; 8:45 am]
BILLING CODE 6820–14–P

[FR Doc. 2018–26580 Filed 12–3–18; 4:15 pm]

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

BILLING CODE 6715–01–P

GENERAL SERVICES
ADMINISTRATION

Centers for Disease Control and
Prevention

[Notice–MA–2018–11; Docket No. 2018–
0002; Sequence 34]

[60Day–19–19BG; Docket No. CDC–2018–
0102]

Rescission of FMR Bulletin

Proposed Data Collection Submitted
for Public Comment and
Recommendations

Office of Government-wide
Policy (OGP); General Services
Administration, (GSA).
ACTION: Notice of Rescission of GSA
Bulletin Federal Management Reguation
(FMR) D–1, Transportation
Management.
AGENCY:

GSA has determined the
guidance for requesting a delegation of
authority for the procurement of
transportation (freight and cargo,
including household goods) and traffic
management services from the
Administrator of General Services to be
administratively burdensome and
ineffective. Therefore, GSA is officially
rescinding GSA Bulletin FMR D–1,
Transportation Management. Agencies

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SUMMARY:

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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

SUMMARY:

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titled ‘‘Web-based approaches to reach
black or African American and
Hispanic/Latino MSM for HIV Testing
and Prevention Services.’’
DATES: CDC must receive written
comments on or before February 4,
2019.
You may submit comments,
identified by Docket No. CDC–2018–
0102 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M.Zirger, Ph.D.,
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 Leroy A.
Richardson, 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;
ADDRESSES:

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Federal Register / Vol. 83, No. 234 / Thursday, December 6, 2018 / Notices
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
Web-based approaches to reach black
or African American and Hispanic/
Latino MSM for HIV Testing and
Prevention Services–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 goal of this study is to evaluate
the effectiveness of mailing out rapid
HIV home-testing kits and additional
testing promotion components to
increase HIV testing among black/
African-American or Hispanic/Latino
MSM. The findings from this research
will assist local and state health
departments, and community based
organizations in making decisions on
how to improve HIV testing and linkage
to HIV prevention services for black/

African American and Hispanic/Latino
men who have sex with men.
The research study is a randomized
control trial and all survey data will be
collected over the internet. There will
not be any in-person surveys. We will
advertise the study on internet websites
frequented by black and Hispanic MSM.
People will click on a banner ad and
will be taken to a study website that
provides a brief overview of the study.
Those who are interested in
participating will complete a brief
survey to determine their eligibility.
Men who are eligible will complete
registration information and then
download a study phone app onto their
smartphone. The app will allow them to
complete a baseline survey. After
completing the baseline survey, they
will be randomized into one of three
conditions.
All participants will be sent a rapid
HIV test kit and they will report their
results to the study. Men assigned to all
study arms will use the study app to
complete study activities. All
participants will have access to webbased HIV counseling upon request.
Participants who report a positive HIV
test result will be offered web-based HIV
counseling if they have not previously
requested counseling. Men assigned to
the control arm will only have access to
the study app and web-based
counseling. Men assigned to one
intervention arm will also be able to
access another smartphone app
(HealthMindr) that will allow them to
engage in additional study activities.
Men assigned to the second intervention
arm will have access to a web-based
forum (HealthEmpowerment) covering

HIV prevention and not the
HealthMindr app. At four months after
enrollment, all participants will
complete an online survey and will be
offered additional HIV testing materials
to complete.
The subpopulation are individuals
who: (1) Identify as African-American/
black or Hispanic/Latino; (2) report their
HIV status as negative or report being
unaware of their HIV status; (3) are not
currently using PrEP or participating in
other HIV testing prevention studies; (4)
have had anal intercourse with another
man in the past 12 months; (5) reside in
one of the study states; (6) Are 18 years
or older; (7) born male; and (8) identify
as male. We will evaluate the
comparative effectiveness of the HIV
home-testing kits and additional testing
promotion components with respect to
linkage of participants to appropriate
services (HIV treatment, PrEP, STI
testing, additional prevention and social
services). These analyses will determine
whether any such differences are
significant within and across study
arms, and by race/ethnicity.
Depending on the study arm to which
participants are assigned, filling out
data collection forms, engaging with
testing promotion components, and
completing and submitting at-home HIV
testing will require between 2 hours 53
minutes and 4 hours and 13 minutes of
a participant’s time over the course of
the entire study period.
The participation of respondents is
voluntary. There is no cost to the
respondents other than their time. The
total estimated annual burden hours for
the proposed project are 7,011 hours.

ESTIMATED ANNUALIZED BURDEN HOURS
Number of respondents

Number of responses per
respondent
per year

10,000
10,000
4,000
3,800
3,600
3,000
3,000
3,000

18
1
1
7
110
10
120
10

10/60
3/60
10/60
5/60
30/60
5/60
30/60
5/60

1667
500
667
317
1,800
250
1,500
250

Enrolled participant .........................

Eligibility Consent ...........................
Eligibility Screener ..........................
Study Consent ................................
Registration contact information .....
Baseline Survey .............................
HIV Test Result Survey ..................
Follow-up Survey ............................
HIV Test Result Survey (completion).
Product ordering .............................

1,200

2

3/60

60

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

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

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

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

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

7,011

Type of respondent

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Potential participant
Potential participant
Potential participant
Potential participant
Enrolled participant
Enrolled participant
Enrolled participant
Enrolled participant

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Form name

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

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Average burden per response (in
Hrs)

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ResponseBurden
(in Hrs)

62866

Federal Register / Vol. 83, No. 234 / Thursday, December 6, 2018 / Notices

Jeffrey M. Zirger,
Acting Lead, Information Collection Review
Office, Office of Scientific Integrity, Office
of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2018–26350 Filed 12–4–18; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–19–0853; Docket No. CDC–2018–
0105]

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 ‘‘Asthma Information Reporting
System (AIRS)’’ (OMB Control No.
0920–0853, expiration date 6/30/2019).
The purpose of AIRS to collect
performance measure and surveillance
data spreadsheets designed to increase
the efficiency and effectiveness of state
asthma programs and to monitor the
impact of the state and national
programs.
DATES: CDC must receive written
comments on or before February 4,
2019.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2018–
0105 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

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SUMMARY:

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20:35 Dec 04, 2018

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(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
Asthma Information and Reporting
System (AIRS)—Revision—National
Center for Environmental Health
(NCEH), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In 1999, the CDC began its National
Asthma Control Program (NACP), a

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public health approach to address the
burden of asthma. The program
supports the goals and objectives of
‘‘Healthy People 2020’’ for asthma, and
is based on the public health principles
of surveillance, partnerships,
interventions, and evaluation. The CDC
requests a 12-month approval to revise
the ‘‘Asthma Information Reporting
System (AIRS)’’ (OMB Control No.
0920–0853; expiration date 6/30/2019).
Specifically, CDC seeks to make the
following changes:
• Increase the number of awardees
from 23 to 25.
• Increase the requested burden hours
from 82 to 89.
• Increase the number of optional
performance measures (PMs) and
decrease the number of required PMs,
while still maintaining a total of 18
PMs.
• Update the instructions for the data
collection instruments to reflect the
optional status of 5 of the 18 PMs and
to clarify instructions that were
commonly misinterpreted.
• Update the Emergency Department
Data and Hospital Discharge Data
reporting forms to include example data
submission templates for each awardee.
Add a tab labeled ‘‘Technical Notes’’
within the Excel reporting form to
collect clarifying information about the
data from each awardee.
• Add examples of Emergency
Department Data and Hospital Discharge
Data reporting forms to provide clarity
on how data should be reported within
the forms.
• Update respondent costs to reflect
current wage data from 2017.
The 12-month approval will allow
CDC to continue to monitor states’
program planning and delivery of public
health activities and the programs’
collaboration with health care systems
for the remainder of the fifth and final
year of cooperative agreement EH14–
1404 (program period: September 2014–
August 2019), and the third and final
year of cooperative agreement EH16–
1606 (program period: September 2016–
August 2019).
The goal of this data collection is to
provide NCEH with routine information
about the activities and performance of
the state and territorial awardees funded
under the NACP through an annual
reporting system. NACP requires
awardees to report activities related to
partnerships, infrastructure, evaluation
and interventions to monitor the state
programs’ performance in reducing the
burden of asthma. AIRS also includes
two forms to collect aggregate ED and
HD data from awardees.
AIRS was first approved by OMB in
2010 to collect data in a web-based

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