Proposed Data Collection Submitted for Public Comment and Recommendations, 51835-51837 [2017-24317]
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Federal Register / Vol. 82, No. 215 / Wednesday, November 8, 2017 / Notices
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remove individuals’ home contact
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17:26 Nov 07, 2017
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Christian S. White,
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[FR Doc. 2017–24243 Filed 11–7–17; 8:45 am]
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51835
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–18–18AF; Docket No. CDC–2018–
0093]
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 generic information collection
project titled ‘‘Assessments to Inform
Program Refinement for HIV, other STD,
and Pregnancy Prevention among
Middle and High-School Aged Youth.’’
CDC seeks to collect qualitative and
quantitative data from adolescents (ages
11–19) and their parents/caregivers to
assess program needs and services.
DATES: CDC must receive written
comments on or before January 8, 2018.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2018–
0093 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Leroy A.
Richardson, Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., MS–D74, Atlanta, Georgia
SUMMARY:
E:\FR\FM\08NON1.SGM
08NON1
51836
Federal Register / Vol. 82, No. 215 / Wednesday, November 8, 2017 / Notices
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.
ethrower on DSK3G9T082PROD with NOTICES
Proposed Project
Assessments to Inform Program
Refinement for HIV, other STD, and
Pregnancy Prevention 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 Centers for Disease Control and
Prevention (CDC) seeks to request OMB
approval of a one-year generic
information collection plan. CDC seeks
to collect qualitative and quantitative
data from adolescents (ages 11–19) and
VerDate Sep<11>2014
17:26 Nov 07, 2017
Jkt 244001
their parents/caregivers to assess
program needs and services.
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 make up
the population of interest for DASH and
several other NCHHSTP divisions, as
Adolescents have specific
developmental, health social, and
resource needs. DASH addresses
adolescent health risk factors and access
to health care as the organization’s
primary mission. The assessment and
research conducted by NCHHSTP is one
pillar upon which NCHHSTP revises
and updates its recommendations and
guidelines. Recommendations and
guidelines for adolescent sexual risk
reduction require a 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 plan intend 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 plan
include:
(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
PO 00000
Frm 00036
Fmt 4703
Sfmt 4703
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
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 crosswalk 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 collect
and copies of data collection
instruments. CDC will pilot test all data
collection instruments. CDC will ensure
cultural, developmental, and age
appropriateness of each instrument.
Similarly, CDC will pilot test parent
data collection instruments 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. CDC will
also adhere to appropriate consent and
assent procedures as outlined in the
IRB-approved protocols and described
in the generic information collection
plan.
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 plan. CDC estimates
57,584 respondent burden hours for
these information collections.
E:\FR\FM\08NON1.SGM
08NON1
51837
Federal Register / Vol. 82, No. 215 / Wednesday, November 8, 2017 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Average
burden
per response
(in hours)
Number of
responses per
respondent
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 .........................
20,000
1
50/60
16,667
Pre/Post youth questionnaire ...........
10,000
2
50/60
16,667
Youth interview/focus group guide ...
3,000
2
1.5
9,000
Parent/Caregiver questionnaire .......
Parent/Caregiver
interview/focus
group guide.
7,500
3,000
2
2
25/60
1.5
6,250
9,000
Total ...........................................
...........................................................
........................
........................
........................
57,584
[60Day–17–17AZG; Docket No. CDC–2017–
0076]
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
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. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (regulations.gov) or by U.S. mail to the
address listed above.
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. 2017–24317 Filed 11–7–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
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 to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed assessment of
cancer prevention services at selected
community mental health centers. CDC
seeks to request an Office of
Management and Budget (OMB)
clearance for a three-year data collection
project.
DATES: Written comments must be
received on or before January 8, 2018.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0076 by any of the following methods:
ethrower on DSK3G9T082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:26 Nov 07, 2017
Jkt 244001
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Leroy A.
Richardson, Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., MS–D74, Atlanta, Georgia
30329; phone: 404–639–7570; Email:
omb@cdc.gov.
SUPPLEMENTARY INFORMATION:
Under the Paperwork Reduction Act
of 1995 (PRA) (44 U.S.C. 3501–3520),
Federal agencies must obtain approval
from the Office of Management and
Budget (OMB) for each collection of
information they conduct or sponsor. In
addition, the PRA also requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each new proposed
collection, each proposed extension of
existing collection of information, and
each reinstatement of previously
approved information collection before
submitting the collection to OMB for
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
Total burden
(in hours)
approval. To comply with this
requirement, we are publishing this
notice of a proposed data collection as
described below.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Assessment of Cancer Prevention
Services at Community Mental Health
Centers—New—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
E:\FR\FM\08NON1.SGM
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]]>Agencies
[Federal Register Volume 82, Number 215 (Wednesday, November 8, 2017)]
[Notices]
[Pages 51835-51837]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-24317]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-18-18AF; Docket No. CDC-2018-0093]
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
generic information collection project titled ``Assessments to Inform
Program Refinement for HIV, other STD, and Pregnancy Prevention among
Middle and High-School Aged Youth.'' CDC seeks to collect qualitative
and quantitative data from adolescents (ages 11-19) and their parents/
caregivers to assess program needs and services.
DATES: CDC must receive written comments on or before January 8, 2018.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2018-
0093 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Leroy A. Richardson, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE., MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (regulations.gov) or by U.S. mail to the address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Leroy A. Richardson, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE., MS-D74, Atlanta, Georgia
[[Page 51836]]
30329; phone: 404-639-7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION:
Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501-
3520), Federal agencies must obtain approval from the Office of
Management and Budget (OMB) for each collection of information they
conduct or sponsor. In addition, the PRA also requires Federal agencies
to provide a 60-day notice in the Federal Register concerning each
proposed collection of information, including each new proposed
collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected; and
4. Minimize the burden of the collection of information on those
who are to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses.
5. Assess information collection costs.
Proposed Project
Assessments to Inform Program Refinement for HIV, other STD, and
Pregnancy Prevention 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 Centers for Disease Control and Prevention (CDC) seeks to
request OMB approval of a one-year generic information collection plan.
CDC seeks to collect qualitative and quantitative data from adolescents
(ages 11-19) and their parents/caregivers to assess program needs and
services.
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 make up the
population of interest for DASH and several other NCHHSTP divisions, as
Adolescents have specific developmental, health social, and resource
needs. DASH addresses adolescent health risk factors and access to
health care as the organization's primary mission. The assessment and
research conducted by NCHHSTP is one pillar upon which NCHHSTP revises
and updates its recommendations and guidelines. Recommendations and
guidelines for adolescent sexual risk reduction require a 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 plan intend
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 plan include:
(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
crosswalk 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 collect and copies of data collection
instruments. CDC will pilot test all data collection instruments. CDC
will ensure cultural, developmental, and age appropriateness of each
instrument. Similarly, CDC will pilot test parent data collection
instruments 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. CDC
will also adhere to appropriate consent and assent procedures as
outlined in the IRB-approved protocols and described in the generic
information collection plan.
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 plan. CDC
estimates 57,584 respondent burden hours for these information
collections.
[[Page 51837]]
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)
----------------------------------------------------------------------------------------------------------------
Middle and High School Age Youth 20,000 1 50/60 16,667
Adolescents. questionnaire.
Middle and High School Age Pre/Post youth 10,000 2 50/60 16,667
Adolescents. questionnaire.
Middle and High School Age Youth interview/ 3,000 2 1.5 9,000
Adolescents. focus group
guide.
Parents/caregivers of Parent/Caregiver 7,500 2 25/60 6,250
adolescents. questionnaire.
Parents/caregivers of Parent/Caregiver 3,000 2 1.5 9,000
adolescents. interview/focus
group guide.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 57,584
----------------------------------------------------------------------------------------------------------------
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. 2017-24317 Filed 11-7-17; 8:45 am]
BILLING CODE 4163-18-P
