Agency Forms Undergoing Paperwork Reduction Act Review, 21235-21237 [2020-07976]
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21235
Federal Register / Vol. 85, No. 74 / Thursday, April 16, 2020 / Notices
acting through NCHS, shall collect
statistics on the extent and nature of
illness and disability of the population
of the United States. The annual
National Health Interview Survey
(NHIS) is a major source of general
statistics on the health of the U.S.
population and has been in the field
continuously since 1957. This voluntary
and confidential household-based
survey collects demographic and healthrelated information from a nationallyrepresentative sample of households
and noninstitutionalized, civilian
persons throughout the country. NHIS
data have long been used by
government, academic, and private
researchers to evaluate both general
health and specific issues, such as
smoking, diabetes, health care coverage,
and access to health care. The survey is
also a leading source of data for the
Congressionally-mandated ‘‘Health US’’
and related publications, as well as the
single most important source of
statistics to track progress toward HHS
health objectives.
The NHIS sample adult and sample
child questionnaires include annual
core content that is scheduled to be
fielded in the survey every year, rotating
content that is fielded periodically,
emerging content to address new topics
of growing interest, and sponsored
content that is fielded when external
funding is available. Rotating sample
adult and sample child core content that
was on the NHIS in 2020 and will rotate
and protection will not be on the 2021
NHIS. New sponsored cancer control
content will focus on screenings for
breast, cervical, prostate, and colon
cancer using similar questions to what
were used in the 2019 NHIS.
Anticipated new sponsored content
include questions on epilepsy
(previously fielded in 2010, 2013, 2015,
and 2017) and occupational health.
Like in past years, and in accordance
with the 1995 initiative to increase the
integration of surveys within the DHHS,
respondents to the 2021 NHIS will serve
as the sampling frame for the Medical
Expenditure Panel Survey conducted by
the Agency for Healthcare Research and
Quality. A subsample of NHIS
respondents and/or members of
commercial survey panels may be
identified to participate in short, webbased methodological and cognitive
testing activities to evaluate the
questionnaire and/or inform the
development of new rotating and
sponsored content using web and/or
mail survey tools. In addition,
subsamples of NHIS respondents may
be recontacted by web, phone, or mail
to ask follow-up questions on topics that
are already included in the NHIS. In the
future, a subsample of NHIS
respondents may also be re-contacted
for a brief health exam. There is no cost
to the respondents other than their time.
Clearance is sought for three years, to
collect data for 2021–2023.
off the 2021 NHIS includes dental
services, other provider services, and
physical activity. Content on walking,
sleep, fatigue, smoking history and
cessation and alcohol use will also
rotate off the sample adult core.
Questions on neighborhood
characteristics, sleep, screen time, and
height and weight will rotate off the
sample child core.
The 2021 sample adult and sample
child rotating core will include
questions about health conditions that
were previously fielded in the 2018
NHIS. The 2021 rotating sample adult
core will include questions on hearing
and communication, psychological
distress, chronic pain, preventive
screening, and aspirin use. The
questions on chronic pain, preventive
screening and aspirin use were all
previously fielded as part of the 2019
rotating core. Questions on
psychological distress and hearing and
communication were previously fielded
as part of the 2018 NHIS. The 2021
sample child rotating core will include
items on stressful life events which
were previously fielded in 2019.
Sponsored content on asthma will be
removed from both the sample adult
and sample child questionnaires.
Sponsored content on cancer control,
immunizations, and diabetes will
remain, but the content will change.
Sponsored cancer control content on
cigarette history, lung cancer screening,
environment for walking and sun care
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total
burden hours
Form name
Adult Household Member .................
Sample Adult .....................................
Adult Family Member ........................
Adult Family Member ........................
Child Family Member ........................
Adult Family Member ........................
Adult Family Member ........................
Household Roster ............................
Adult Questionnaire ..........................
Child Questionnaire ..........................
Methodological Projects ...................
NHIS Follow-up survey ....................
Health Exam .....................................
Reinterview Survey ..........................
36,000
30,000
10,000
15,000
3,000
10,000
5,500
1
1
1
1
1
1
1
5/60
40/60
20/60
20/60
20/60
45/60
5/60
3,000
20,600
3,334
5,000
1,000
7,500
458
Total ...........................................
...........................................................
........................
........................
........................
40,892
Jeffrey M. Zirger,
Lead, Information Collection Review Office
Office of Scientific Integrity Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–07977 Filed 4–15–20; 8:45 am]
BILLING CODE 4163–18–P
jbell on DSKJLSW7X2PROD with NOTICES
Number of
respondents
Type of respondent
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30-Day–20–1180]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
VerDate Sep<11>2014
18:20 Apr 15, 2020
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Frm 00074
Fmt 4703
Sfmt 4703
has submitted the information
collection request titled Airline and
Vessel Traveler Information Collection
(42 CFR part 71) 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 December
23, 2019 to obtain comments from the
public and affected agencies. CDC
received two comments related to the
previous notice. This notice serves to
E:\FR\FM\16APN1.SGM
16APN1
21236
Federal Register / Vol. 85, No. 74 / Thursday, April 16, 2020 / Notices
allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
jbell on DSKJLSW7X2PROD with NOTICES
Proposed Project
Airline and Vessel Traveler
Information Collection (42 CFR part 71)
(OMB Control No. 0920–1180, Exp. 05/
31/2020)—Revision—Division of Global
Migration and Quarantine (DGMQ),
National Center for Emerging Zoonotic
and Infectious Diseases (NCEZID),
Centers for Disease Control and
Prevention (CDC).
VerDate Sep<11>2014
18:20 Apr 15, 2020
Jkt 250001
Background and Brief Description
Under the Public Health Service Act
(42 United States Code § 264), and
under 42 Code of Federal Regulations
(CFR) §§ 71.4 and 71.5, CDC can order
air carriers and maritime vessels
arriving from another country to submit
a certain information related to
passengers and crew that CDC believes
were exposed to or infected with a
communicable disease that poses a risk
of spread in the United States.
Stopping a communicable disease
outbreak—whether it is naturally
occurring or intentionally caused—
requires the use of the most rapid and
effective public health tools available.
Basic public health practices, such as
collaborating with airlines in the
identification and notification of
potentially exposed contacts, are critical
tools in the fight against the
introduction, transmission, and spread
of communicable diseases in the United
States.
The collection of pertinent contact
information enables Quarantine Public
Health Officers in CDC’s Division of
Global Migration and Quarantine
(DGMQ) to notify state and local health
departments in order for them to make
contact with individuals who may have
been exposed to a communicable
disease during travel and identify
appropriate public health interventions.
In the event that there is a confirmed
case or suspected exposure of
communicable disease of public health
concern aboard an aircraft or maritime
vessel, or an outbreak in a geographic
location, CDC can require that airlines
provide certain traveler contact
information at risk for exposure. The
information collection differs depending
on the communicable disease that is
confirmed or suspected during air or
maritime travel, or in a geographic
location during an outbreak. CDC uses
this passenger and crew manifest
information to coordinate with state and
local health departments so they can
follow-up with residents who live or are
currently located in their jurisdiction. In
general, state and local health
departments are responsible for this
public health follow-up. In rare cases,
CDC may use the manifest data to
perform the contact investigation
directly. In either case, CDC works with
state and local health departments so
that individuals can receive appropriate
public health follow-up.
This revision is requesting minor
changes to the verbiage of the
international manifest order forms used
under 42 CFR 71.4(a) and (b) to clarify
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Frm 00075
Fmt 4703
Sfmt 4703
the information required by CDC to
conduct a contact investigation and to
provide general grammatical
improvements to enhance clarity. The
number of estimated international
manifests ordered from the air carriers
in response to a confirmed case or
suspected exposure after arrival is
increased given CDC’s experience with
the 2019 measles outbreak and the
current COVID–19 outbreak.
Additionally, under the Interim Final
Rule published on February 7, 2020
adding 42 CFR 71.4(d),and the
subsequent February 18, 2020 Order
under 42 CFR 71.31 and 71.4, CDC is
seeking through this revision to update
the estimated burden and outline the
information collection process
associated with the requirement that
airlines collect contact information from
travelers and provide that information
to CDC via existing mechanisms, such
as PNR, APIS, and eAPIS, on a
continuous basis following an order
from the Director.
While CDC can require maritime
vessels to submit traveler information
under 42 CFR 71.5, this happens very
rarely (less than 10 times on an annual
basis) and so the burden is not
accounted for in this Notice.
The total estimated hourly burden to
respondents as a result of this
information collection is 1,835,134
hours per year. While CDC has included
maritime conveyance manifest orders in
the public health rationale for this
information collection, these orders
occur less than 10 times a year and are
not included in the burden table. CDC
does not anticipate any cost burden to
respondents under the manifest process
as outlined in 42 CFR 71.4(a) and (b), as
this only requires airlines to provide the
information if it is available and
maintained.
Under the February 7, 2020 IFR, CDC
anticipates that some 12 US major
carriers and 61 major foreign carriers
will modify their data systems, or
contract with third party reservation
system providers, to ensure that the
information required under the IFR is
transmitted using existing mechanisms
to CBP (e.g., PNR, APIS, eAPIS). CDC
estimates that these changes will cost
approximately $700,000 per carrier for a
total cost of $51,100,000. Smaller
revenue airlines will also have access to
eAPIS to submit the information if they
do not plan to modify their data
systems. That functionality is already
available under the management of U.S.
Customs and Border Protection.
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16APN1
21237
Federal Register / Vol. 85, No. 74 / Thursday, April 16, 2020 / Notices
Number of
responses per
respondent
Average
burden per
response
(in hours)
Form name
Airline Medical Officer or Equivalent/Computer and Information Systems Manager.
Airline Medical Officer or Equivalent/Computer and Information Systems Manager.
International Passengers (3rd party disclosure).
Airline staff ......................................................
International TB Manifest Template ...............
51
1
360/60
International Non-TB Manifest Template .......
249
1
360/60
No Form .........................................................
110,000,000
1
.5/60
No Form .........................................................
110,000,000
1
.5/60
Jeffrey M. Zirger,
Acting Lead, Information Collection Review
Office, Office of Scientific Integrity, Office
of Science, Centers for Disease Control and
revention.
[FR Doc. 2020–07976 Filed 4–15–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30-Day–20–1072]
Agency Forms Undergoing Paperwork
Reduction Act Review
jbell on DSKJLSW7X2PROD with NOTICES
Number of
respondents
Type of respondent
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘The Enhanced
STD surveillance Network (SSuN)’’ 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 Friday, October 25, 2019, to
obtain comments from the public and
affected agencies. CDC did not receive
comments related to the previous
notice. This notice serves to allow an
additional 30 days for public and
affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
VerDate Sep<11>2014
18:20 Apr 15, 2020
Jkt 250001
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
The Enhanced STD surveillance
Network (SSuN), (OMB Control No.
0920–1072 Exp. 09/30/2021)—
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 National Center for HIV/AIDS,
Viral Hepatitis, STD and TB Prevention
(NCHHSTP) is requesting revision of the
information collection entitled
‘‘Enhanced STD Surveillance Network
(SSuN)’’. Revisions to this submission
include adding reported adult syphilis
cases to enhanced case-based
surveillance records, addition of 87 new
data elements, removal of 115 data
elements associated with a discontinued
neurosyphilis surveillance activity and
revision of methods to include Health
PO 00000
Frm 00076
Fmt 4703
Sfmt 4703
Department surveillance HIV registry
matching activities for patients
presenting for care in STD clinical
facilities. This revision also includes
changes to the number and identity of
collaborating jurisdictions from 10 to 11
sites as a result of a recent notice of
funding opportunity. The estimate of
annualized burden hours for this data
collection increases modestly from
4,134 hours to 6,303 hours for the
revised project as a result of revisions
and expanding the project from 10 to 11
awardees for the current data collection
cycle.
The purpose of this project is to
enhance capacity for STD surveillance
and better meet CDC’s disease
surveillance mandate by; (1) providing
more comprehensive information on
reported cases of notifiable STDs to
enhance the ability of public health
authorities to interpret trends in case
incidence, assess inequalities in the
burden of disease by population
characteristics and to monitor STD
treatment and selected adverse health
outcomes of STDs, and, (2) to monitor
STD and HIV co-infection, screening,
uptake of high-impact HIV prevention
and health care access trends among
patients seeking care and those
diagnosed with STDs in specific clinical
settings.
Routine STD surveillance activities
are ongoing in all US states and
jurisdictions, and cases are reported to
CDC through the National Notifiable
Disease Surveillance System (NNDSS).
However, case reports are often missing
critical patient demographics and are of
limited scope with respect to risk
behavior, provider and clinical
information, treatment, co-infection and
partner characteristics—data that are
needed to appropriately direct disease
control activities. Enhanced SSuN is the
only current surveillance infrastructure
providing information on patient and
partner characteristics, clinical
presentation, screening and uptake of
HIV testing, treatment patterns, provider
compliance with treatment
recommendations, HIV co-infection
among persons diagnosed with STDs
E:\FR\FM\16APN1.SGM
16APN1
Agencies
[Federal Register Volume 85, Number 74 (Thursday, April 16, 2020)]
[Notices]
[Pages 21235-21237]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-07976]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30-Day-20-1180]
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 Airline and Vessel Traveler Information
Collection (42 CFR part 71) 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 December 23, 2019 to obtain comments from the public and
affected agencies. CDC received two comments related to the previous
notice. This notice serves to
[[Page 21236]]
allow an additional 30 days for public and affected agency comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) Minimize the burden of the collection of information on those
who are to respond, including, through the use of appropriate
automated, electronic, mechanical, or other technological collection
techniques or other forms of information technology, e.g., permitting
electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570. Comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. Direct
written comments and/or suggestions regarding the items contained in
this notice to the Attention: CDC Desk Officer, Office of Management
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202)
395-5806. Provide written comments within 30 days of notice
publication.
Proposed Project
Airline and Vessel Traveler Information Collection (42 CFR part 71)
(OMB Control No. 0920-1180, Exp. 05/31/2020)--Revision--Division of
Global Migration and Quarantine (DGMQ), National Center for Emerging
Zoonotic and Infectious Diseases (NCEZID), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Under the Public Health Service Act (42 United States Code Sec.
264), and under 42 Code of Federal Regulations (CFR) Sec. Sec. 71.4
and 71.5, CDC can order air carriers and maritime vessels arriving from
another country to submit a certain information related to passengers
and crew that CDC believes were exposed to or infected with a
communicable disease that poses a risk of spread in the United States.
Stopping a communicable disease outbreak--whether it is naturally
occurring or intentionally caused--requires the use of the most rapid
and effective public health tools available. Basic public health
practices, such as collaborating with airlines in the identification
and notification of potentially exposed contacts, are critical tools in
the fight against the introduction, transmission, and spread of
communicable diseases in the United States.
The collection of pertinent contact information enables Quarantine
Public Health Officers in CDC's Division of Global Migration and
Quarantine (DGMQ) to notify state and local health departments in order
for them to make contact with individuals who may have been exposed to
a communicable disease during travel and identify appropriate public
health interventions.
In the event that there is a confirmed case or suspected exposure
of communicable disease of public health concern aboard an aircraft or
maritime vessel, or an outbreak in a geographic location, CDC can
require that airlines provide certain traveler contact information at
risk for exposure. The information collection differs depending on the
communicable disease that is confirmed or suspected during air or
maritime travel, or in a geographic location during an outbreak. CDC
uses this passenger and crew manifest information to coordinate with
state and local health departments so they can follow-up with residents
who live or are currently located in their jurisdiction. In general,
state and local health departments are responsible for this public
health follow-up. In rare cases, CDC may use the manifest data to
perform the contact investigation directly. In either case, CDC works
with state and local health departments so that individuals can receive
appropriate public health follow-up.
This revision is requesting minor changes to the verbiage of the
international manifest order forms used under 42 CFR 71.4(a) and (b) to
clarify the information required by CDC to conduct a contact
investigation and to provide general grammatical improvements to
enhance clarity. The number of estimated international manifests
ordered from the air carriers in response to a confirmed case or
suspected exposure after arrival is increased given CDC's experience
with the 2019 measles outbreak and the current COVID-19 outbreak.
Additionally, under the Interim Final Rule published on February 7,
2020 adding 42 CFR 71.4(d),and the subsequent February 18, 2020 Order
under 42 CFR 71.31 and 71.4, CDC is seeking through this revision to
update the estimated burden and outline the information collection
process associated with the requirement that airlines collect contact
information from travelers and provide that information to CDC via
existing mechanisms, such as PNR, APIS, and eAPIS, on a continuous
basis following an order from the Director.
While CDC can require maritime vessels to submit traveler
information under 42 CFR 71.5, this happens very rarely (less than 10
times on an annual basis) and so the burden is not accounted for in
this Notice.
The total estimated hourly burden to respondents as a result of
this information collection is 1,835,134 hours per year. While CDC has
included maritime conveyance manifest orders in the public health
rationale for this information collection, these orders occur less than
10 times a year and are not included in the burden table. CDC does not
anticipate any cost burden to respondents under the manifest process as
outlined in 42 CFR 71.4(a) and (b), as this only requires airlines to
provide the information if it is available and maintained.
Under the February 7, 2020 IFR, CDC anticipates that some 12 US
major carriers and 61 major foreign carriers will modify their data
systems, or contract with third party reservation system providers, to
ensure that the information required under the IFR is transmitted using
existing mechanisms to CBP (e.g., PNR, APIS, eAPIS). CDC estimates that
these changes will cost approximately $700,000 per carrier for a total
cost of $51,100,000. Smaller revenue airlines will also have access to
eAPIS to submit the information if they do not plan to modify their
data systems. That functionality is already available under the
management of U.S. Customs and Border Protection.
[[Page 21237]]
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondent Form name respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Airline Medical Officer or Equivalent/ International TB 51 1 360/60
Computer and Information Systems Manifest Template.
Manager.
Airline Medical Officer or Equivalent/ International Non-TB 249 1 360/60
Computer and Information Systems Manifest Template.
Manager.
International Passengers (3rd party No Form................. 110,000,000 1 .5/60
disclosure).
Airline staff......................... No Form................. 110,000,000 1 .5/60
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Acting Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
revention.
[FR Doc. 2020-07976 Filed 4-15-20; 8:45 am]
BILLING CODE 4163-18-P