60 Day FRN

Federal Register / Vol. 79, No. 96 / Monday, May 19, 2014 / Notices
Consequently, although financial, legal,
and clerical personnel may be involved
in the information collection process,
FTC staff now assumes that midmanagement personnel and outside
legal counsel will handle most of the
tasks involved in gathering and
producing responsive information, and
has applied an average rate of $250/hour
for all labor costs. Thus the labor costs
per company may range between
$68,750 (275 hours × $250/hour) and
$211,250 (845 hours × $250/hour).

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C. Estimated Annual Capital or Other
Non-labor Costs
Staff anticipates that the capital or
other non-labor costs associated with
the information requests will be
minimal. Although the information
requests may require the respondent to
store copies of the requested
information provided to the
Commission, responding Firms should
already have in place the means to store
information of the volume requested.
Respondents may need to purchase
minimal office supplies to respond to
the request. Staff estimates that each
respondent will spend $500 for such
costs regarding the information request,
for a total additional non-labor cost
burden of $20,000 ($500 × 40 Firms).
V. Request for Comment
Under the PRA, 44 U.S.C. 3501–3521,
federal agencies must obtain approval
from OMB for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ means
agency requests or requirements that
members of the public submit reports,
keep records, or provide information to
a third party. 44 U.S.C. 3502(3); 5 CFR
1320.3(c). As required by Section
3506(c)(2) of the PRA, 44 U.S.C. 3506,
on October 3, 2013, the FTC published
its First Notice seeking public
comments on a study of PAE activity.
The FTC will provide OMB with the
comments received in response to the
First Notice.
Pursuant to Section 3507 of the PRA,
additional public comments regarding
this information collection request may
be submitted to OMB and the FTC.
Comments received by June 18, 2014
will be considered. Written comments
to OMB should be addressed to: Office
of Information and Regulatory Affairs,
Office of Management and Budget,
Attention: Desk Officer for the Federal
Trade Commission, New Executive
Office Building, Docket Library, Room
10102, 725 17th Street NW.,
Washington, DC 20503. Comments sent
to OMB by U.S. postal mail, however,
are subject to delays due to heightened
security precautions. Thus, comments

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instead should be sent by facsimile to
(202) 395–5167.
Postal mail addressed to the
Commission is also subject to delay due
to heightened security screening. As a
result, we encourage you to submit your
comments online. To submit your
comment to the FTC online, write ‘‘PAE
Reports: Paperwork Comment; Project
No. P131203’’ on your comment, and
file your comment online at https://
ftcpublic.commentworks.com/ftc/
paestudypra2, by following the
instructions on the web-based form. If
you prefer to file your comment on
paper, mail your comment to the
following address: Federal Trade
Commission, Office of the Secretary,
600 Pennsylvania Avenue NW., Suite
CC–5610, (Annex J), Washington, DC
20580, or deliver your comment to the
following address: Federal Trade
Commission, Office of the Secretary,
Constitution Center, 400 7th Street SW.,
5th Floor, Suite 5610, (Annex J),
Washington, DC 20024. If this Notice
appears at http://www.regulations.gov/
#!home, you also may file a comment
through that Web site.
Your comment, including your name
and your state, will be placed on the
public record of this proceeding,
including, to the extent practicable, on
the public Commission Web site, at
http://www.ftc.gov/os/
publiccomments.shtm. As a matter of
discretion, the Commission tries to
remove individuals’ home contact
information from comments before
placing them on the Commission Web
site.
Because your comment will be made
public, you are solely responsible for
making sure that your comment does
not include any sensitive personal
information, like anyone’s Social
Security number, date of birth, driver’s
license number or other state
identification number or foreign country
equivalent, passport number, financial
account number, or credit or debit card
number.
You are also solely responsible for
making sure that your comment does
not include any sensitive health
information, like medical records or
other individually identifiable health
information. In addition, do not include
any ‘‘[t]rade secret or any commercial or
financial information which is * * *
privileged or confidential,’’ as discussed
in Section 6(f) of the FTC Act, 15 U.S.C.
46(f), and FTC Rule 4.10(a)(2), 16 CFR
4.10(a)(2). In particular, do not include
competitively sensitive information
such as costs, sales statistics,
inventories, formulas, patterns, devices,
manufacturing processes, or customer
names in your comment.

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If you seek confidential treatment for
your comment, you must file it in paper
form, with a request for confidential
treatment, and you must follow the
procedure explained in FTC Rule 4.9(c),
16 CFR 4.9(c).3 Your comment will be
kept confidential only if the FTC
General Counsel grants your request in
accordance with the law and the public
interest.
Visit the Commission Web site at
http://www.ftc.gov to read this Notice
and the news release describing it. The
FTC Act and other laws that the
Commission administers permit the
collection of public comments to
consider and use in this proceeding as
appropriate. The Commission will
consider all timely and responsive
public comments that it receives on or
before June 18, 2014. You can find more
information, including routine uses
permitted by the Privacy Act, in the
Commission’s privacy policy, at http://
www.ftc.gov/ftc/privacy.htm.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. 2014–11484 Filed 5–16–14; 8:45 am]
BILLING CODE 6750–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–14–14AAO]

Proposed Data Collections Submitted
for Public Comment and
Recommendations
The Centers for Disease Control and
Prevention (CDC), as part of its
continuing effort to reduce public
burden, 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. To
request more information on the below
proposed project or to obtain a copy of
the information collection plan and
instruments, call 404–639–7570 or send
comments to LeRoy Richardson, 1600
Clifton Road, MS–D74, Atlanta, GA
30333 or send an email to omb@cdc.gov.
Comments submitted in response to
this notice will be summarized and/or
included in the request for Office of
3 In particular, the written request for confidential
treatment that accompanies the comment must
include the factual and legal basis for the request,
and must identify the specific portions of the
comment to be withheld from the public record. See
FTC Rule 4.9(c), 16 CFR 4.9(c).

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Federal Register / Vol. 79, No. 96 / Monday, May 19, 2014 / Notices

Management and Budget (OMB)
approval. 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. Written comments should
be received within 60 days of this
notice.

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Proposed Project
Testing Act Early Messages and
Materials for ‘‘Learn the Signs. Act
Early.’’—Phase II,—New—National
Center on Birth Defects and
Developmental Disabilities (NCBDDD),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Developmental milestones are used to
track growth and development in
children. Various milestones correspond
to specific stages in a child’s growth and
development (e.g. crawling, walking,
smiling, and waving ‘‘bye-bye’’). Not all
children develop at the same pace;
however, these developmental
milestones serve as a guide in
monitoring children as they grow.
According to the CDC, approximately
one in six children in the United States
have developmental-behavioral

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disabilities such as autism, intellectual
disability, or attention-deficit/
hyperactivity disorder. Despite the fact
that most of these children will show
mild developmental delays (i.e., failing
to reach some of the milestones
associated with their stage of
development) by the age of two, less
than half of these children will be
identified before they start school.
Missing this window of opportunity for
diagnosing developmental delays in
children creates a serious public health
problem. The late identification of
developmental delays can lead to
increased costs for future interventions
and can be detrimental to the child’s
ability to learn.
The CDC initiated the ‘‘Learn the
Signs. Act Early.’’ (LTSAE) campaign in
2004 in an effort to improve the
likelihood that children with
developmental disabilities are identified
and connected with appropriate services
at the earliest age possible. To this end,
one of the campaign’s overall goals is to
empower parents to ‘‘act early’’ if they
have concerns about their child’s
development. Children from families
insured by Medicaid and those from
families with low incomes are often
identified with developmental delays
and disabilities at a later age than other
children, and thus are the target
audience for the campaign.
The study described in this
information collection request seeks to
assess the impact of ‘‘act early’’
messages embedded within LTSAE
campaign materials. To achieve this
goal, CDC will work with a contractor,
Westat, to test revised draft messages
and materials with low-income parents
through focus groups and intercept
interviews administered via the web on
a tablet device. Parents/guardians who
are age 18–55 and who have children
age 5 or younger will be recruited from
six primary care practices (3 in the
Washington, DC/Baltimore, Maryland
metropolitan area and three in the
Atlanta, Georgia metropolitan area) to
participate in focus groups and/or an
intercept interview.
Selected primary care practices will
see children from low-income families
as part of their patient population. Each
of the six selected practices will receive
study promotional materials, including
a poster to hang in the office and
waiting room as well as handouts to
leave at the front desk. These materials

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will advertise the focus groups and
outline eligibility criteria.
Parents interested in participating
will be advised to call an 800 number
to be screened and scheduled for a
group discussion (if eligible). The 800
number will be staffed by the Westat
study team who will be responsible for
screening and scheduling.
Representatives from each of the
practices will be provided with brief
‘‘talking points’’ and study (Frequently
Asked Questions (FAQs) to refer to if
interested parents have any basic
questions about the study.
It is estimated that 80 respondents
will have to be screened in order to
recruit 40 participants for the focus
groups. Each screening will take
approximately five minutes. The
estimated response burden for the
screening process is seven hours. The
focus groups will have 10 participants
each. Four focus groups will be
conducted in two locations (the
metropolitan areas of Atlanta, Georgia
and Washington, DC/Baltimore,
Maryland), yielding a total of 40
participants. Parents/guardians will be
asked to complete an informed consent,
which will take approximately 15
minutes to review, and the focus group
discussion using the moderator’s guide
will take 60 minutes to complete. Focus
group activities will have a total burden
of 50 hours.
The intercept interviews will take
place in the waiting rooms or right
outside the waiting rooms if feasible.
Parents will be recruited as they are
waiting for their appointment. Again, it
is estimated that 80 respondents will
have to be screened in order to recruit
40 participants. The screening process
should take approximately five minutes.
The estimated response burden for the
screening process is seven hours. We
plan to conduct a total of 40 intercept
interviews. Twenty interviews will be
conducted in each of two locations
(Atlanta, Georgia metropolitan area and
Washington, DC/Baltimore, Maryland
metropolitan area). The intercept
interview will be conducted as a
computer-assisted personal interview
(CAPI) and will take each respondent
approximately 15 minutes to complete,
for an estimated total burden of 10
hours.
The total estimated burden for this
data collection is 74 hours. There is no
cost to respondents other than their
time.

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Federal Register / Vol. 79, No. 96 / Monday, May 19, 2014 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent

Average
burden per
response
(in hours)

Number of
responses per
respondent

Number of
respondents

Form name

Total burden
hours

Focus Groups
Parents/Guardians .............................
Parents/Guardians .............................
Parents/Guardians .............................

Screener ..........................................
Informed Consent ............................
Focus Group Moderator’s Guide .....

80
40
40

1
1
1

5/60
15/60
1

7
10
40

Intercept Interviews
Parents/Guardians .............................
Parents/Guardians .............................

Screener ..........................................
Intercept Interview ...........................

80
40

1
1

5/60
15/60

7
10

Total ...........................................

..........................................................

........................

........................

........................

74

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. 2014–11449 Filed 5–16–14; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: National Extranet Optimized
Runaway and Homeless Youth

Management Information System
(NEORHYMIS) Version 3.0.
OMB No.: 0970–0123.
Description: The Runaway and
Homeless Youth Act, as amended by
Public Law 106–71 (42 U.S.C. 5701 et
seq.), mandates that the Department of
Health and Human Services (HHS)
report regularly to Congress on the
status of HHS-funded programs serving
runaway and homeless youth. Such
reporting is similarly mandated by the
Government Performance and Results
Act. Organizations funded under the
Runaway and Homeless Youth program
are required by statute (42 U.S.C. 5712,
42 U.S.C. 5714–2) to meet certain data
collection and reporting requirements.
These requirements include
maintenance of client statistical records
on the number and the characteristics of

the runaway and homeless youth, and
youth at risk of family separation, who
participate in the project, and the
services provided to such youth by the
project.
Respondents: States localities, private
entities and coordinated networks of
such entities. Typical respondents are
non-profit community based
organizations who are reporting on the
youth that they serve through their
Basic Center, Transitional Living and
Street Outreach programs.

ANNUAL BURDEN ESTIMATES
Number of
respondents

Instrument

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Youth Profile: Basic Center Program (one for each youth) ..........................
Youth Profile: Transitional Living Program (one for each youth) ..................
Youth Profile: Street Outreach Program (one for each youth) ......................
Brief Contacts (4 data elements per youth) ..................................................
BCP/TLP Turnaways (5data elements per youth) .........................................
Data Transfer .................................................................................................

Estimated Total Annual Burden
Hours: 61,300.
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,

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Number of
responses per
respondent

Average burden
hours per
response

118
16
6,186
153
33
1

0.20
0.250
0.073
0.05
0.05
0.50

291
199
108
491
491
599

Attn: ACF Reports Clearance Officer.
Email address: infocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
The Department specifically requests
comments 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)
the quality, utility, and clarity of the
information to be collected; and (d)

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Total burden
hours
6,868
796
48,770
3,756
810
300

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.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2014–11417 Filed 5–16–14; 8:45 am]
BILLING CODE 4184–01–P

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