Proposed Data Collection Submitted for Public Comment and Recommendations, 62864-62866 [2018-26350]
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Federal Register / Vol. 83, No. 234 / Thursday, December 6, 2018 / Notices
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[FR Doc. 2018–26409 Filed 12–4–18; 8:45 am]
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[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
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AGENCY:
GSA has determined the
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Transportation Management. Agencies
khammond on DSK30JT082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
20:35 Dec 04, 2018
Jkt 247001
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:
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
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:
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;
ADDRESSES:
E:\FR\FM\06DEN1.SGM
06DEN1
62865
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
khammond on DSK30JT082PROD with NOTICES
Potential participant
Potential participant
Potential participant
Potential participant
Enrolled participant
Enrolled participant
Enrolled participant
Enrolled participant
VerDate Sep<11>2014
Form name
........................
........................
........................
........................
.........................
.........................
.........................
.........................
20:35 Dec 04, 2018
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E:\FR\FM\06DEN1.SGM
Average burden per response (in
Hrs)
06DEN1
Total
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
khammond on DSK30JT082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
20:35 Dec 04, 2018
Jkt 247001
(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
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
PO 00000
Frm 00034
Fmt 4703
Sfmt 4703
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
E:\FR\FM\06DEN1.SGM
06DEN1
]]>Agencies
[Federal Register Volume 83, Number 234 (Thursday, December 6, 2018)]
[Notices]
[Pages 62864-62866]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-26350]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-19-19BG; Docket No. CDC-2018-0102]
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 ``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.
ADDRESSES: 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;
[[Page 62865]]
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 web-based 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
Number of responses per Average burden Total
Type of respondent Form name respondents respondent per per response ResponseBurden
year (in Hrs) (in Hrs)
----------------------------------------------------------------------------------------------------------------
Potential participant......... Eligibility 10,000 18 10/60 1667
Consent.
Potential participant......... Eligibility 10,000 1 3/60 500
Screener.
Potential participant......... Study Consent... 4,000 1 10/60 667
Potential participant......... Registration 3,800 7 5/60 317
contact
information.
Enrolled participant.......... Baseline Survey. 3,600 110 30/60 1,800
Enrolled participant.......... HIV Test Result 3,000 10 5/60 250
Survey.
Enrolled participant.......... Follow-up Survey 3,000 120 30/60 1,500
Enrolled participant.......... HIV Test Result 3,000 10 5/60 250
Survey
(completion).
Enrolled participant.......... Product ordering 1,200 2 3/60 60
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 7,011
----------------------------------------------------------------------------------------------------------------
[[Page 62866]]
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
