Agency Forms Undergoing Paperwork Reduction Act Review, 13750-13751 [2018-06391]
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13750
Federal Register / Vol. 83, No. 62 / Friday, March 30, 2018 / Notices
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than April 27, 2018.
A. Federal Reserve Bank of Dallas
(Robert L. Triplett III, Senior Vice
President) 2200 North Pearl Street,
Dallas, Texas 75201–2272:
1. A.N.B. Holding Company, Ltd.,
Terrell, Texas; to acquire voting shares
of The ANB Corporation, Terrell, Texas,
and indirectly acquire The American
National Bank of Texas, Terrell, Texas
and Lakeside Bancshares, Inc.,
Rockwall, Texas, and indirectly acquire
Lakeside National Bank, Rockwall,
Texas.
Board of Governors of the Federal Reserve
System, March 27, 2018.
Ann E. Misback,
Secretary of the Board.
[FR Doc. 2018–06473 Filed 3–29–18; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–18–18AF]
amozie on DSK30RV082PROD with NOTICES
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 ‘‘Assessing the
impact of interventions to decrease
sexual risk behaviors and adverse health
outcomes 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
8, 2017 to obtain comments from the
public and affected agencies. CDC
received three 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
VerDate Sep<11>2014
18:57 Mar 29, 2018
Jkt 244001
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 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
Assessing the Impact of Interventions
to Decrease Sexual Risk Behaviors and
Adverse Health Outcomes Among
Middle and High School-Aged Youth—
New—Division of Adolescent and
School Health (DASH), National Center
for HIV/AIDS, Viral Hepatitis, STD, and
TB Prevention, Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The CDC requests approval for a new
generic information collection package
that supports collection of quantitative
and qualitative information from
adolescents (ages 11–19) and their
parents/caregivers for the purpose of
assessing and informing programs and
services to reduce sexual risk behaviors
and decrease adverse health outcomes
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
PO 00000
Frm 00030
Fmt 4703
Sfmt 4703
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 (e.g.,
sexual minority youth, homeless youth)
and that provide more tailored sexual
risk reduction programs and services to
them.
The CDC requests a three-year OMB
approval for a new generic information
collection request plan entitled,
‘‘Assessing the Impact of Interventions
to Decrease Sexual Risk Behaviors and
Adverse Health Outcomes among
Middle and High School-aged Youth.’’
The information collection requests
under this generic plan 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 sexual risk
reduction or adverse health outcomes
among adolescents of middle- and highschool age.
(2) Qualitative data collection through
electronic, telephone, or paper means to
gather information about programmatic
and service activities related to sexual
risk reduction or prevention of adverse
health outcomes among adolescents of
middle- and high-school age.
Qualitative data collection may involve
focus groups and in-depth interviewing
E:\FR\FM\30MRN1.SGM
30MRN1
13751
Federal Register / Vol. 83, No. 62 / Friday, March 30, 2018 / Notices
through group interviews, and cognitive
interviewing.
For adolescents, data collection
instruments will include questions on
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 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.
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. Participation of
respondents is voluntary. There is no
cost to the participants other than their
time.
The table below provides the
estimated annualized response burden
for up to 15 individual data collections
under this generic information
collection plan 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.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
Adolescents .....................................................
Adolescents .....................................................
Parents of adolescents ...................................
Adolescents .....................................................
Parents of adolescents ...................................
Youth questionnaire .......................................
Pre/Post youth questionnaire .........................
Adult questionnaire ........................................
Youth interview/focus group protocol .............
Adult interview/focus group protocol ..............
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2018–06391 Filed 3–29–18; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–18–0910]
amozie on DSK30RV082PROD with NOTICES
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 Message Testing
for Tobacco Communication Activities
(MTTCA) 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
13, 2017 to obtain comments from the
public and affected agencies. CDC did
VerDate Sep<11>2014
18:57 Mar 29, 2018
Jkt 244001
not receive comments related to the
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments. CDC’s
Office on Smoking and Health has used
the MTTCA clearance to support the
development and testing of tobaccorelated health messages, including
messages supporting CDC’s National
Tobacco Education Campaign (NTEC)
called the Tips from Former Smokers®
campaign.
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
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
20,000
10,000
7,500
3,000
3,000
1
2
2
2
2
Average
burden per
response
(in hours)
50/60
50/60
25/60
1.5
1.5
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
Message Testing for Tobacco
Communication Activities
(MTTCA)(OMB Control Number 0920–
0910, expires 03/31/2018)—Extension—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
E:\FR\FM\30MRN1.SGM
30MRN1
]]>Agencies
[Federal Register Volume 83, Number 62 (Friday, March 30, 2018)]
[Notices]
[Pages 13750-13751]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-06391]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-18-18AF]
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 ``Assessing the impact of interventions to
decrease sexual risk behaviors and adverse health outcomes 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 8, 2017 to obtain comments from the public and
affected agencies. CDC received three 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;
(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 [email protected]. 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
Assessing the Impact of Interventions to Decrease Sexual Risk
Behaviors and Adverse Health Outcomes Among Middle and High School-Aged
Youth--New--Division of Adolescent and School Health (DASH), National
Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers
for Disease Control and Prevention (CDC).
Background and Brief Description
The CDC requests approval for a new generic information collection
package that supports collection of quantitative and qualitative
information from adolescents (ages 11-19) and their parents/caregivers
for the purpose of assessing and informing programs and services to
reduce sexual risk behaviors and decrease adverse health outcomes 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 (e.g., sexual
minority youth, homeless youth) and that provide more tailored sexual
risk reduction programs and services to them.
The CDC requests a three-year OMB approval for a new generic
information collection request plan entitled, ``Assessing the Impact of
Interventions to Decrease Sexual Risk Behaviors and Adverse Health
Outcomes among Middle and High School-aged Youth.'' The information
collection requests under this generic plan 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 sexual risk reduction or adverse health
outcomes 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 sexual risk reduction or prevention of adverse
health outcomes among adolescents of middle- and high-school age.
Qualitative data collection may involve focus groups and in-depth
interviewing
[[Page 13751]]
through group interviews, and cognitive interviewing.
For adolescents, data collection instruments will include questions
on 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 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.
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. Participation of respondents is voluntary.
There is no cost to the participants other than their time.
The table below provides the estimated annualized response burden
for up to 15 individual data collections under this generic information
collection plan 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.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondents Form name respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Adolescents........................... Youth questionnaire..... 20,000 1 50/60
Adolescents........................... Pre/Post youth 10,000 2 50/60
questionnaire.
Parents of adolescents................ Adult questionnaire..... 7,500 2 25/60
Adolescents........................... Youth interview/focus 3,000 2 1.5
group protocol.
Parents of adolescents................ Adult interview/focus 3,000 2 1.5
group protocol.
----------------------------------------------------------------------------------------------------------------
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2018-06391 Filed 3-29-18; 8:45 am]
BILLING CODE 4163-18-P
