Agency Forms Undergoing Paperwork Reduction Act Review, 11096-11098 [2019-05556]
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11096
Federal Register / Vol. 84, No. 57 / Monday, March 25, 2019 / Notices
indicated above or following the last
call for comments, whichever is earlier.
Members of the public who wish to
address the NIOSH BSC are requested to
contact the Executive Secretary for
scheduling purposes (see contact
information below). Alternatively,
written comments to the BSC may be
submitted via an on-line form at the
following website: https://www.cdc.gov/
niosh/bsc/contact.html. Each
commenter will be provided up to five
minutes for comment. A limited number
of time slots are available and will be
assigned on a first come-first served
basis. Written comments will also be
accepted from those unable to attend the
public session via an on-line form at the
following website: https://www.cdc.gov/
niosh/bsc/contact.html. The meeting is
also open to the public via webcast. If
you wish to attend in person or by
webcast, please see the NIOSH website
to register (https://www.cdc.gov/niosh/
bsc/) or call (404–498–2539) at least five
business days in advance of the
meeting. Teleconference is available
toll-free; please dial (888) 397–9578,
Participant Pass Code 63257516. Adobe
Connect webcast will be available at
https://odniosh.adobeconnect.com/
nioshbsc/ for participants wanting to
connect remotely.
DATES: The meeting will be held on May
30, 2019, 8:30 a.m.–2:30 p.m., EDT.
ADDRESSES: Patriots Plaza I, 395 E Street
SW, Room 9000, Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT:
Alberto Garcia, MS, Executive Secretary,
BSC, NIOSH, CDC, 1090 Tusculum
Avenue, MS–R5, Cincinnati, OH 45226,
telephone (513) 841–4596, fax (513)
841–4506, or email at agarcia1@cdc.gov.
SUPPLEMENTARY INFORMATION:
Purpose: The Secretary, the Assistant
Secretary for Health, and by delegation
the Director, Centers for Disease Control
and Prevention, are authorized under
Sections 301 and 308 of the Public
Health Service Act to conduct directly
or by grants or contracts, research,
experiments, and demonstrations
relating to occupational safety and
health and to mine health. The Board of
Scientific Counselors provides guidance
to the Director, National Institute for
Occupational Safety and Health on
research and prevention programs.
Specifically, the Board provides
guidance on the Institute’s research
activities related to developing and
evaluating hypotheses, systematically
documenting findings and
disseminating results. The Board
evaluates the degree to which the
activities of the National Institute for
Occupational Safety and Health: (1)
Conform to appropriate scientific
VerDate Sep<11>2014
16:47 Mar 22, 2019
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standards, (2) address current, relevant
needs, and (3) produce intended results.
Matters to be Considered: The agenda
for the meeting addresses occupational
safety and health issues related to:
NIOSH Chemical Risk Management;
Occupational Exposure Banding;
Research Integration Activities; and an
Overview of the National Fire Fighter
Registry. Agenda items are subject to
change as priorities dictate. An agenda
is also posted on the NIOSH website
(https://www.cdc.gov/niosh/bsc/).
The Chief Operating Officer, Centers
for Disease Control and Prevention, has
been delegated the authority to sign
Federal Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Agenda: To review and evaluate grant
applications.
For Further Information Contact: Hylan
Shoob, Ph.D., Scientific Review Officer,
Center for Global Health, CDC, 1600 Clifton
Drive, Atlanta, GA 30329–4027, (404) 639–
4796; HShoob@cdc.gov.
The Chief Operating Officer, Centers for
Disease Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for both
the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Sherri Berger,
Chief Operating Officer, Centers for Disease
Control and Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2019–05590 Filed 3–22–19; 8:45 am]
BILLING CODE 4163–18–P
Sherri Berger,
Chief Operating Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2019–05591 Filed 3–22–19; 8:45 am]
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
[30Day–19–1235]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency Forms Undergoing Paperwork
Reduction Act Review
Centers for Disease Control and
Prevention
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Assessments to
Inform Program Refinement for HIV,
other STD, and Pregnancy Prevention
among Middle and High-School Aged
Youth, 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 November 15, 2018 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;
Notice of Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended, and the Determination of
the Chief Operating Officer, CDC,
pursuant to Public Law 92–463. The
grant applications and the discussions
could disclose confidential trade secrets
or commercial property such as
patentable material, and personal
information concerning individuals
associated with the grant applications,
the disclosure of which would
constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Disease, Disability,
and Injury Prevention and Control Special
Emphasis Panel (SEP)—GH16–003,
Conducting Public Health Research in
Thailand: technical collaboration with the
Ministry of Public Health in the Kingdom of
Thailand (MOPH); GH16–006, Conducting
Public Health Research in Kenya; and GH19–
005, Advancing Public Health Research in
Bangladesh.
Date: April 23, 2019.
Time: 9:00 a.m.–2:00 p.m., EDT
Place: Teleconference.
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Federal Register / Vol. 84, No. 57 / Monday, March 25, 2019 / Notices
(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 or
send an email to omb@cdc.gov. 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
Assessments to Inform Program
Refinement for HIV, other STD, and
Pregnancy Prevention among Middle
and High-School Aged Youth (OMB
Control No. 0920–1235, Expiration 06/
30/19)—Extension—National Center for
HIV/AIDS, Viral Hepatitis, STD, TB
Prevention, Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) requests three year
OMB approval for the Extension of a
Generic information collection package
(OMB #0920–1235) that supports
collection of quantitative and qualitative
information from adolescents (ages 11–
19) and their parents/caregivers for the
purpose of needs assessment and
program refinement for programs and
services to prevent HIV, other sexually
transmitted diseases (STDs), and
pregnancy among middle and high
school aged adolescents.
NCHHSTP conducts behavioral and
health service assessments and research
projects as part of its response to the
domestic HIV/AIDS epidemic, STD
prevention, TB elimination and viral
hepatitis control with national, state,
and local partners. Adolescents are a
population with specific developmental,
health and social, and resource needs,
and their health risk factors and access
to health care are addressed as a
VerDate Sep<11>2014
16:47 Mar 22, 2019
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primary mission by the Division of
Adolescent and School Health (DASH),
and adolescents are a population of
interest for several other NCHHSTP
divisions. The assessment and research
conducted by NCHHSTP is one pillar
upon which recommendations and
guidelines are revised and updated.
Recommendations and guidelines for
adolescent sexual risk reduction require
that foundation of scientific evidence.
Assessment of programmatic practices
for adolescents helps to assure effective
and evidence-based sexual risk
reduction practices and efficient use of
resources. Such assessments also help to
improve programs through better
identification of strategies relevant to
adolescents as a population as well as
specific sub-groups of adolescents at
highest risk for HIV and other STDs so
that programs can be better tailored for
them.
The information collection requests
under this generic package are intended
to allow for data collection with two
types of respondents:
• Adolescents (11–19 years old) of
middle and high school age; and
• Parents and/or caregivers of
adolescents of middle and high school
age. For the purposes of this generic
package, parents/caregivers include the
adult primary caregiver(s) for a child’s
basic needs (e.g., food, shelter, and
safety). This includes biological parents;
other biological relatives such as
grandparents, aunts, uncles, or siblings;
and non-biological parents such as
adoptive, foster, or stepparents.
The types of information collection
activities included in this generic
package are:
(1) Quantitative data collection
through electronic, telephone, or paper
questionnaires to gather information
about programmatic and service
activities related to the prevention of
HIV and other STDs among adolescents
of middle- and high-school age.
(2) Qualitative data collection through
electronic, telephone, or paper means to
gather information about programmatic
and service activities related to the
prevention of HIV and other STDs
among adolescents of middle- and highschool age. Qualitative data collection
may involve focus groups and in-depth
interviewing through group interviews,
and cognitive interviewing.
For adolescents, data collection
instruments will include questions on
demographic characteristics;
experiences with programs and services
to reduce the risk of HIV and other STD
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11097
transmission; and knowledge, attitudes,
behaviors, and skills related to sexual
risk and protective factors on the
individual, interpersonal, and
community levels.
For parents and caregivers, data
collection instruments will include
questions on demographic
characteristics as well as parents’/
caregivers’ (1) perceptions about
programs and services provided to
adolescents; (2) knowledge, attitudes,
and perceptions about their adolescents’
health risk and protective behaviors;
and (3) parenting knowledge, attitudes,
behaviors, and skills.
Any data collection request put
forward under this generic clearance
will identify the programs and/or
services to be informed or refined with
the information from the collection and
will include a cross-walk of data
elements to the aspects of the program
the project team seeks to inform or
refine. Because this request includes a
wide range of possible data collection
instruments, specific requests will
include items of information to be
collected and copies of data collection
instruments. It is expected that all data
collection instruments will be pilottested, and will be culturally,
developmentally, and age appropriate
for the adolescent populations included.
Similarly, parent data collection
instruments will be pilot-tested, and the
data collection instruments will reflect
the culture, developmental stage, and
age of the parents’ adolescent children.
All data collection procedures will
receive review and approval by an
Institutional Review Board for the
Protection of Human Subjects and
follow appropriate consent and assent
procedures as outlined in the IRBapproved protocols, and these will be
described in the individual information
collection requests put forward under
this generic package.
The table below provides the
estimated annualized response burden
for up to 15 individual data collections
per year under this generic clearance at
57,584 hours. Average burden per
response is based on pilot testing and
timing of quantitative and qualitative
instrument administration during
previous studies. Response times
include the time to read and respond to
consent forms and to read or listen to
instructions. Participation of
respondents is voluntary. There is no
cost to the participants other than their
time.
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11098
Federal Register / Vol. 84, No. 57 / Monday, March 25, 2019 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
Middle and High School Age Adolescents .....
Middle and High School Age Adolescents .....
Middle and High School Age Adolescents .....
Parents/caregivers of adolescents ..................
Parents/caregivers of adolescents ..................
Youth Questionnaire ......................................
Pre/Post youth questionnaire .........................
Youth interview/focus group guide .................
Parent/Caregiver questionnaire .....................
Parent/Caregiver interview/focus group guide
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–05556 Filed 3–22–19; 8:45 am]
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[CDC–2018–0103; Docket Number NIOSH–
322]
Final National Occupational Research
Agenda for Immune, Infectious, and
Dermal Disease Prevention (IID)
National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS).
ACTION: Notice of availability.
AGENCY:
NIOSH announces the
availability of the final National
Occupational Research Agenda for
Immune, Infectious, and Dermal Disease
Prevention.
DATES: The final document was
published March 19, 2019 on the CDC
website.
ADDRESSES: The document may be
obtained at the following link: https://
www.cdc.gov/nora/councils/iid/
agenda.html.
FOR FURTHER INFORMATION CONTACT:
Emily Novicki, M.A., M.P.H,
(NORACoordinator@cdc.gov), National
Institute for Occupational Safety and
Health, Centers for Disease Control and
Prevention, Mailstop E–20, 1600 Clifton
Road NE, Atlanta, GA 30329, phone
(404) 498–2581 (not a toll free number).
SUPPLEMENTARY INFORMATION: On
November 8, 2018, NIOSH published a
request for public review in the Federal
Register [83 FR 55887] of the draft
version of the National Occupational
Research Agenda for Immune,
Infectious, and Dermal Disease
Jkt 247001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
1
2
2
2
2
50/60
50/60
90/60
25/60
90/60
Job Titles and/or Job Duties: All
laborers who worked in any area at the
Y–12 Plant in Oak Ridge, Tennessee,
fabricating or processing uranium
during the period from January 1, 1977,
through December 31, 1994.
Period of Employment: January 1,
1977 through December 31, 1994.
[FR Doc. 2019–05586 Filed 3–22–19; 8:45 am]
BILLING CODE 4163–19–P
Centers for Disease Control
Decision To Evaluate a Petition To
Designate a Class of Employees From
the Y–12 Plant in Oak Ridge,
Tennessee, To Be Included in the
Special Exposure Cohort
National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention, Department of Health
and Human Services.
ACTION: Notice.
AGENCY:
SUMMARY:
20,000
10,000
3,000
7,500
3,000
Average
burden per
response
(in hours)
John J. Howard,
Director, National Institute for Occupational
Safety and Health.
BILLING CODE 4163–19–P
Centers for Disease Control and
Prevention
16:47 Mar 22, 2019
Frank J. Hearl,
Chief of Staff, National Institute for
Occupational Safety and Health, Centers for
Disease Control and Prevention.
[FR Doc. 2019–05561 Filed 3–22–19; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
VerDate Sep<11>2014
Prevention. All comments received were
reviewed and addressed where
appropriate.
Number of
responses per
respondent
NIOSH gives notice of a
decision to evaluate a petition to
designate a class of employees from the
Y–12 Plant in Oak Ridge, Tennessee, to
be included in the Special Exposure
Cohort under the Energy Employees
Occupational Illness Compensation
Program Act of 2000.
FOR FURTHER INFORMATION CONTACT:
Stuart L. Hinnefeld, Director, Division
of Compensation Analysis and Support,
National Institute for Occupational
Safety and Health, 1090 Tusculum
Avenue, MS C–46, Cincinnati, OH
45226–1938, Telephone 877–222–7570.
Information requests can also be
submitted by email to DCAS@CDC.GOV.
SUPPLEMENTARY INFORMATION:
Authority: 42 CFR 83.9–83.12.
Pursuant to 42 CFR 83.12, the initial
proposed definition for the class being
evaluated, subject to revision as
warranted by the evaluation, is as
follows:
Facility: Y–12 Plant.
Location: Oak Ridge, Tennessee.
SUMMARY:
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–19–18APX]
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 Dental Survey:
Improving Outpatient Antibiotic Use
through Implementation and Evaluation
of Core Elements of Outpatient
Antibiotic Stewardship 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 August
10, 2018 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
E:\FR\FM\25MRN1.SGM
25MRN1
]]>Agencies
[Federal Register Volume 84, Number 57 (Monday, March 25, 2019)]
[Notices]
[Pages 11096-11098]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-05556]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-19-1235]
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 Assessments to Inform Program Refinement for
HIV, other STD, and Pregnancy Prevention among Middle and High-School
Aged Youth, 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 November
15, 2018 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;
[[Page 11097]]
(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 or send an email to omb@cdc.gov. 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
Assessments to Inform Program Refinement for HIV, other STD, and
Pregnancy Prevention among Middle and High-School Aged Youth (OMB
Control No. 0920-1235, Expiration 06/30/19)--Extension--National Center
for HIV/AIDS, Viral Hepatitis, STD, TB Prevention, Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) requests three
year OMB approval for the Extension of a Generic information collection
package (OMB #0920-1235) that supports collection of quantitative and
qualitative information from adolescents (ages 11-19) and their
parents/caregivers for the purpose of needs assessment and program
refinement for programs and services to prevent HIV, other sexually
transmitted diseases (STDs), and pregnancy among middle and high school
aged adolescents.
NCHHSTP conducts behavioral and health service assessments and
research projects as part of its response to the domestic HIV/AIDS
epidemic, STD prevention, TB elimination and viral hepatitis control
with national, state, and local partners. Adolescents are a population
with specific developmental, health and social, and resource needs, and
their health risk factors and access to health care are addressed as a
primary mission by the Division of Adolescent and School Health (DASH),
and adolescents are a population of interest for several other NCHHSTP
divisions. The assessment and research conducted by NCHHSTP is one
pillar upon which recommendations and guidelines are revised and
updated. Recommendations and guidelines for adolescent sexual risk
reduction require that foundation of scientific evidence. Assessment of
programmatic practices for adolescents helps to assure effective and
evidence-based sexual risk reduction practices and efficient use of
resources. Such assessments also help to improve programs through
better identification of strategies relevant to adolescents as a
population as well as specific sub-groups of adolescents at highest
risk for HIV and other STDs so that programs can be better tailored for
them.
The information collection requests under this generic package are
intended to allow for data collection with two types of respondents:
Adolescents (11-19 years old) of middle and high school
age; and
Parents and/or caregivers of adolescents of middle and
high school age. For the purposes of this generic package, parents/
caregivers include the adult primary caregiver(s) for a child's basic
needs (e.g., food, shelter, and safety). This includes biological
parents; other biological relatives such as grandparents, aunts,
uncles, or siblings; and non-biological parents such as adoptive,
foster, or stepparents.
The types of information collection activities included in this
generic package are:
(1) Quantitative data collection through electronic, telephone, or
paper questionnaires to gather information about programmatic and
service activities related to the prevention of HIV and other STDs
among adolescents of middle- and high-school age.
(2) Qualitative data collection through electronic, telephone, or
paper means to gather information about programmatic and service
activities related to the prevention of HIV and other STDs among
adolescents of middle- and high-school age. Qualitative data collection
may involve focus groups and in-depth interviewing through group
interviews, and cognitive interviewing.
For adolescents, data collection instruments will include questions
on demographic characteristics; experiences with programs and services
to reduce the risk of HIV and other STD transmission; and knowledge,
attitudes, behaviors, and skills related to sexual risk and protective
factors on the individual, interpersonal, and community levels.
For parents and caregivers, data collection instruments will
include questions on demographic characteristics as well as parents'/
caregivers' (1) perceptions about programs and services provided to
adolescents; (2) knowledge, attitudes, and perceptions about their
adolescents' health risk and protective behaviors; and (3) parenting
knowledge, attitudes, behaviors, and skills.
Any data collection request put forward under this generic
clearance will identify the programs and/or services to be informed or
refined with the information from the collection and will include a
cross-walk of data elements to the aspects of the program the project
team seeks to inform or refine. Because this request includes a wide
range of possible data collection instruments, specific requests will
include items of information to be collected and copies of data
collection instruments. It is expected that all data collection
instruments will be pilot-tested, and will be culturally,
developmentally, and age appropriate for the adolescent populations
included. Similarly, parent data collection instruments will be pilot-
tested, and the data collection instruments will reflect the culture,
developmental stage, and age of the parents' adolescent children. All
data collection procedures will receive review and approval by an
Institutional Review Board for the Protection of Human Subjects and
follow appropriate consent and assent procedures as outlined in the
IRB-approved protocols, and these will be described in the individual
information collection requests put forward under this generic package.
The table below provides the estimated annualized response burden
for up to 15 individual data collections per year under this generic
clearance at 57,584 hours. Average burden per response is based on
pilot testing and timing of quantitative and qualitative instrument
administration during previous studies. Response times include the time
to read and respond to consent forms and to read or listen to
instructions. Participation of respondents is voluntary. There is no
cost to the participants other than their time.
[[Page 11098]]
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Middle and High School Age Adolescents Youth Questionnaire..... 20,000 1 50/60
Middle and High School Age Adolescents Pre/Post youth 10,000 2 50/60
questionnaire.
Middle and High School Age Adolescents Youth interview/focus 3,000 2 90/60
group guide.
Parents/caregivers of adolescents..... Parent/Caregiver 7,500 2 25/60
questionnaire.
Parents/caregivers of adolescents..... Parent/Caregiver 3,000 2 90/60
interview/focus group
guide.
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2019-05556 Filed 3-22-19; 8:45 am]
BILLING CODE 4163-18-P
