Proposed Data Collection Submitted for Public Comment and Recommendations, 32184-32185 [2019-14305]
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32184
Federal Register / Vol. 84, No. 129 / Friday, July 5, 2019 / Notices
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–14299 Filed 7–3–19; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–19–0770; Docket No. CDC–2019–
0054]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled National HIV Behavioral
Surveillance System (NHBS). CDC is
requesting approval for a revision to the
previously approved project to continue
collecting standardized HIV-related
behavioral data from persons at risk for
HIV, selected from up to 25
Metropolitan Statistical Areas (MSAs)
throughout the United States.
DATES: CDC must receive written
comments on or before September 3,
2019.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2019–
0054 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
jbell on DSK3GLQ082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:54 Jul 03, 2019
Jkt 247001
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.
FOR FURTHER INFORMATION CONTACT:
Proposed Project
National HIV Behavioral Surveillance
System (NHBS)—(OMB Control No.
0920–0770, Exp. 05/31/2020)—
Revision—National Center for HIV/
AIDS, Viral Hepatitis, STD, and TB
Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The purpose of this data collection is
to monitor behaviors of persons at high
PO 00000
Frm 00066
Fmt 4703
Sfmt 4703
risk for infection that are related to
Human Immunodeficiency Virus (HIV)
transmission and prevention in the
United States. The primary objectives of
the NHBS are to obtain data from
samples of persons at risk to: (a)
Describe the prevalence and trends in
risk behaviors; (b) describe the
prevalence of and trends in HIV testing
and HIV infection; (c) describe the
prevalence of and trends in use of HIV
prevention services; (d) identify met and
unmet needs for HIV prevention
services in order to inform health
departments, community based
organizations, community planning
groups and other stakeholders.
By describing and monitoring the HIV
risk behaviors, HIV seroprevalence and
incidence, and HIV prevention
experiences of persons at highest risk
for HIV infection, NHBS provides an
important data source for evaluating
progress towards national public health
goals, such as reducing new infections,
increasing the use of condoms, and
targeting high-risk groups.
The Centers for Disease Control and
Prevention requests approval for a threeyear revision of this information
collection. Data are collected through
anonymous, in-person interviews
conducted with persons systematically
selected from up to 25 Metropolitan
Statistical Areas (MSAs) throughout the
United States; these 25 MSAs are
chosen based on having high HIV
prevalence. Persons at risk for HIV
infection to be interviewed for NHBS
include men who have sex with men
(MSM), persons who inject drugs (IDU),
and heterosexually active persons at
increased risk of HIV infection (HET). A
brief screening interview will be used to
determine eligibility for participation in
the behavioral assessment.
The data from the behavioral
assessment will provide estimates of (1)
behavior related to the risk of HIV and
other sexually transmitted diseases, (2)
prior testing for HIV, (3) and use of HIV
prevention services.
All persons interviewed will also be
offered an HIV test, and will participate
in a pre-test counseling session. No
other federal agency systematically
collects this type of information from
persons at risk for HIV infection. These
data have substantial impact on
prevention program development and
monitoring at the local, state, and
national levels.
CDC estimates that NHBS will
involve, per year in up to 25 MSAs,
eligibility screening for 100 persons and
eligibility screening plus the behavioral
assessment with 500 eligible
respondents, resulting in a total of
37,500 eligible survey respondents and
E:\FR\FM\05JYN1.SGM
05JYN1
32185
Federal Register / Vol. 84, No. 129 / Friday, July 5, 2019 / Notices
7,500 ineligible screened persons during
a three-year period. Data collection will
rotate such that interviews will be
conducted among one group per year:
MSM in Year 1, IDU in Year 2, and HET
in Year 3. The type of data collected for
each group will vary slightly due to
different sampling methods and risk
characteristics of the group.
Participation of respondents is
voluntary and there is no cost to the
respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)
Total burden
(in hours)
Form name
Persons Screened ............................
Eligible Participants ...........................
Eligible Participants ...........................
Eligible Participant ............................
Peer Recruiters .................................
Eligibility Screener ............................
Behavioral Assessment MSM ..........
Behavioral Assessment IDU ............
Behavioral Assessment HET ...........
Recruiter Debriefing .........................
15,000
4,167
4,167
4,167
4,167
1
1
1
1
1
5/60
24/60
43/60
31/60
2/60
1,250
1,667
2,986
2,153
139
Total ...........................................
...........................................................
........................
........................
........................
8,195
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–14305 Filed 7–3–19; 8:45 am]
BILLING CODE 4163–18–P
health system level changes to support
prevention and management of diabetes
and heart disease.
DATES: CDC must receive written
comments on or before September 3,
2019.
You may submit comments,
identified by Docket No. CDC–2019–
0055 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7570; Email: 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
ADDRESSES:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–19–19BHC; Docket No. CDC–19–
0055]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled EVALUATION OF THE DP18–
1815 COOPERATIVE AGREEMENT
PROGRAM: IMPROVING THE HEALTH
OF AMERICANS THROUGH
PREVENTION AND MANAGEMENT OF
DIABETES AND HEART DISEASE AND
STROKE. The purpose of data collection
is to determine CDC-funded recipients’
progress towards using DP18–1815
funds to implement evidence-based
strategies, and to determine how those
efforts are contributing to state level and
SUMMARY:
jbell on DSK3GLQ082PROD with NOTICES
Number of
responses per
respondent
Number of
respondents
Type of respondents
VerDate Sep<11>2014
17:54 Jul 03, 2019
Jkt 247001
PO 00000
Frm 00067
Fmt 4703
Sfmt 4703
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
Evaluation of the DP18–1815
Cooperative Agreement Program:
Improving the Health of Americans
Through Prevention and Management of
Diabetes and Heart Disease and Stroke—
New—National Center for Chronic
Disease Prevention and Health
Promotion, Centers for Disease Control
and Prevention (CDC).
E:\FR\FM\05JYN1.SGM
05JYN1
]]>Agencies
[Federal Register Volume 84, Number 129 (Friday, July 5, 2019)]
[Notices]
[Pages 32184-32185]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-14305]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-19-0770; Docket No. CDC-2019-0054]
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 National HIV Behavioral
Surveillance System (NHBS). CDC is requesting approval for a revision
to the previously approved project to continue collecting standardized
HIV-related behavioral data from persons at risk for HIV, selected from
up to 25 Metropolitan Statistical Areas (MSAs) throughout the United
States.
DATES: CDC must receive written comments on or before September 3,
2019.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2019-
0054 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (regulations.gov) or by U.S. mail to the address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email:
[email protected].
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected; and
4. Minimize the burden of the collection of information on those
who are to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses.
5. Assess information collection costs.
Proposed Project
National HIV Behavioral Surveillance System (NHBS)--(OMB Control
No. 0920-0770, Exp. 05/31/2020)--Revision--National Center for HIV/
AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The purpose of this data collection is to monitor behaviors of
persons at high risk for infection that are related to Human
Immunodeficiency Virus (HIV) transmission and prevention in the United
States. The primary objectives of the NHBS are to obtain data from
samples of persons at risk to: (a) Describe the prevalence and trends
in risk behaviors; (b) describe the prevalence of and trends in HIV
testing and HIV infection; (c) describe the prevalence of and trends in
use of HIV prevention services; (d) identify met and unmet needs for
HIV prevention services in order to inform health departments,
community based organizations, community planning groups and other
stakeholders.
By describing and monitoring the HIV risk behaviors, HIV
seroprevalence and incidence, and HIV prevention experiences of persons
at highest risk for HIV infection, NHBS provides an important data
source for evaluating progress towards national public health goals,
such as reducing new infections, increasing the use of condoms, and
targeting high-risk groups.
The Centers for Disease Control and Prevention requests approval
for a three-year revision of this information collection. Data are
collected through anonymous, in-person interviews conducted with
persons systematically selected from up to 25 Metropolitan Statistical
Areas (MSAs) throughout the United States; these 25 MSAs are chosen
based on having high HIV prevalence. Persons at risk for HIV infection
to be interviewed for NHBS include men who have sex with men (MSM),
persons who inject drugs (IDU), and heterosexually active persons at
increased risk of HIV infection (HET). A brief screening interview will
be used to determine eligibility for participation in the behavioral
assessment.
The data from the behavioral assessment will provide estimates of
(1) behavior related to the risk of HIV and other sexually transmitted
diseases, (2) prior testing for HIV, (3) and use of HIV prevention
services.
All persons interviewed will also be offered an HIV test, and will
participate in a pre-test counseling session. No other federal agency
systematically collects this type of information from persons at risk
for HIV infection. These data have substantial impact on prevention
program development and monitoring at the local, state, and national
levels.
CDC estimates that NHBS will involve, per year in up to 25 MSAs,
eligibility screening for 100 persons and eligibility screening plus
the behavioral assessment with 500 eligible respondents, resulting in a
total of 37,500 eligible survey respondents and
[[Page 32185]]
7,500 ineligible screened persons during a three-year period. Data
collection will rotate such that interviews will be conducted among one
group per year: MSM in Year 1, IDU in Year 2, and HET in Year 3. The
type of data collected for each group will vary slightly due to
different sampling methods and risk characteristics of the group.
Participation of respondents is voluntary and there is no cost to
the respondents 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)
----------------------------------------------------------------------------------------------------------------
Persons Screened.............. Eligibility 15,000 1 5/60 1,250
Screener.
Eligible Participants......... Behavioral 4,167 1 24/60 1,667
Assessment MSM.
Eligible Participants......... Behavioral 4,167 1 43/60 2,986
Assessment IDU.
Eligible Participant.......... Behavioral 4,167 1 31/60 2,153
Assessment HET.
Peer Recruiters............... Recruiter 4,167 1 2/60 139
Debriefing.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 8,195
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2019-14305 Filed 7-3-19; 8:45 am]
BILLING CODE 4163-18-P
