Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Evaluation of the Food and Drug Administration's ‘Fresh Empire’ Multicultural Youth Tobacco Prevention Campaign, 19673-19675 [2015-08466]
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Federal Register / Vol. 80, No. 70 / Monday, April 13, 2015 / Notices
identify the guidance you are
requesting.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
IV. Paperwork Reduction Act of 1995
Food and Drug Administration
This guidance refers to previously
approved collections of information
found in FDA regulations. These
collections of information are subject to
review by the Office of Management and
Budget (OMB) under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3520). The collections of information in
21 CFR part 801 have been approved
under OMB control number 0910–0485;
the collections of information in 21 CFR
part 803 have been approved under
OMB control number 0910–0437; the
collections of information in 21 CFR
part 812 have been approved under
OMB control number 0910–0073; the
collections of information in 21 CFR
part 822 have been approved under
OMB control number 0910–0449; the
collection of information in 21 CFR part
860, subpart C have been approved
under OMB control number 0910–0138;
and the collections of information in the
guidance document regarding requests
for feedback on medical device
submission have been approved under
OMB control number 0910–0756.
[Docket No. FDA–2014–N–2294]
V. Comments
Interested persons may submit either
electronic comments regarding this
document to https://www.regulations.gov
or written comments to the Division of
Dockets Management (see ADDRESSES). It
is only necessary to send one set of
comments. Identify comments with the
docket number found in brackets in the
heading of this document. Received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday, and
will be posted to the docket at https://
www.regulations.gov.
Dated: April 7, 2015.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2015–08363 Filed 4–10–15; 8:45 am]
mstockstill on DSK4VPTVN1PROD with NOTICES
BILLING CODE 4164–01–P
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Evaluation of the
Food and Drug Administration’s ‘Fresh
Empire’ Multicultural Youth Tobacco
Prevention Campaign
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by May 13,
2015.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or emailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–NEW and
title ‘‘Evaluation of the Food and Drug
Administration’s ‘Fresh Empire’
Multicultural Youth Tobacco Prevention
Campaign.’’ Also include the FDA
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT: FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002, PRAStaff@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUMMARY:
Evaluation of the Food and Drug
Administration’s ‘Fresh Empire’
Multicultural Youth Tobacco
Prevention Campaign (OMB Control
Number 0910–NEW)
The 2009 Family Smoking Prevention
and Tobacco Control Act (Tobacco
Control Act) (Pub. L. 111–31) amended
the Federal Food, Drug, and Cosmetic
Act (the FD&C Act) to grant FDA
authority to regulate the manufacture,
marketing, and distribution of tobacco
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18:02 Apr 10, 2015
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19673
products to protect public health and to
reduce tobacco use by minors. Section
1003(d)(2)(D) of the FD&C Act (21
U.S.C. 393(d)(2)(D)) supports the
development and implementation of
FDA public education campaigns
related to tobacco use. Accordingly,
FDA is currently developing and
implementing a youth-targeted public
education campaign (‘Fresh Empire’) to
help prevent tobacco use among
multicultural youth and thereby reduce
the public health burden of tobacco. The
campaign will feature events,
advertisements on television and radio
and in print, digital communications
including social media, and other forms
of media.
In support of the provisions of the
Tobacco Control Act that require FDA to
protect the public health and to reduce
tobacco use by minors, FDA requests
OMB approval to collect information
needed to evaluate FDA’s ‘Fresh
Empire’ multicultural youth tobacco
prevention campaign. Comprehensive
evaluation of FDA’s public education
campaigns is needed to ensure
campaign messages are effectively
received, understood, and accepted by
those for whom they are intended.
Evaluation is an essential organizational
practice in public health and a
systematic way to account for and
improve public health actions.
FDA plans to evaluate the
effectiveness of its multicultural youth
tobacco prevention campaign through
an outcome evaluation study that will
be designed to follow the multiple,
discrete waves of media advertising
planned for the campaign.
The outcome evaluation study
consists of a pre-test survey of
multicultural youth aged 12 to 17 before
campaign launch. The pre-test survey
will be followed by ongoing crosssectional surveys of the target audience
of youth beginning approximately 3
months following campaign launch.
Information will be collected about
youth awareness of and exposure to
campaign events and advertisements
and about tobacco-related knowledge,
attitudes, beliefs, intentions, and use.
Information will also be collected on
demographic variables including age,
sex, race/ethnicity, grade level, and
primary language.
All information will be collected
through in-person and Web-based
questionnaires. Youth respondents will
be recruited from two sources: (1) A
sample drawn from 30 U.S. media
markets gathered using an addressbased postal mail sampling of U.S.
households for the outcome evaluation
studies and (2) targeted social media
E:\FR\FM\13APN1.SGM
13APN1
19674
Federal Register / Vol. 80, No. 70 / Monday, April 13, 2015 / Notices
(e.g., Facebook). Participation in the
study is voluntary.
The information collected is
necessary to inform FDA’s efforts and
measure the effectiveness and public
health impact of the campaign. Data will
be used to estimate awareness of and
exposure to the campaign among youth
in target markets where the campaign is
active. Data will also be used to examine
statistical associations between
exposure to the campaign and
subsequent changes in specific
outcomes of interest, which will include
knowledge, attitudes, and beliefs,
related to tobacco use.
FDA’s burden estimate is based on
prior experience with in-person and
Internet panel studies similar to the
Agency’s plan presented in this
document. Since the 60-day notice
published, FDA has revised the
estimated burden. The original burden
estimate accounted for evaluation of
more than one FDA multicultural
campaign. The current burden estimate
accounts for the evaluation of one
campaign, FDA’s ‘Fresh Empire’ Youth
Tobacco Prevention Campaign.
A mail-based screener will be one of
the methods used to identify eligible
youth. Parents or guardians will be
asked to provide consent and their
contact information on this form. For
the pre-launch survey, the 5-minute
screener will be completed by 13,816
households for a total of 1,151 burden
hours for youth and an additional 230
hours for the parents or guardians. For
the pre-test survey, 2,100 youth will
complete a questionnaire with an
estimated burden of 30 minutes per
respondent, for an annualized total of
1,050 hours. For the post-test screening
survey, the estimated burden is 3,453
hours for youth and 691 hours for
adults. For the post-test surveys, the
estimated burden is 45 minutes per
respondent, for a total of 4,725 burden
hours.
We will also recruit youth through
social media (e.g., Facebook, Twitter) as
a secondary strategy to recruit youth 13
to 17. An online version of the screener
described above will be used to identify
eligible youth (included in Attachment
3). Eligible youth will be asked to
provide their parents’ or guardians’
contact information. The screener will
take 5 minutes and will be completed by
2,500 youth for the pre-test survey for a
total of 208 burden hours. Of these, 500
will be eligible and complete the pretest survey for a total of 250 burden
hours. For the post-test survey, 10,500
youth will complete the 5-minute
screener, for 875 burden hours. Of these,
2,100 will be eligible and complete the
post-test survey online (up to 45
minutes), for a total of 1,575 burden
hours.
The target number of completed
campaign questionnaires for all
respondents is 134,528, and the
annualized response burden is
estimated at 14,208 hours.
In the Federal Register of January 5,
2015 (80 FR 230), FDA published a 60day notice requesting public comment
on the proposed collection of
information. Two comments were
received, however, only one was PRA
related.
Comment: One comment stated that
the media tracking survey and the
outcome evaluation study proposed by
FDA are critical to FDA’s efforts to
develop and implement an effective
multicultural youth tobacco prevention
campaign.
Response: FDA agrees that this
collection of information is necessary to
the Agency’s efforts to promote and
improve public health.
FDA estimates the burden of this
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1
Number of
respondents
Type of respondent
Activity
Youth aged 12 to 17 in the
United States.
Screener and Consent
Process—Pre-test outcome survey.
Screener and Consent
Process—Pre-test outcome survey.
Screener and Consent
Process—post-test outcome survey.
Screener and Consent
Process—post-test outcome survey.
Pre-test outcome evaluation
survey.
Number of
responses per
respondent
Total annual
responses
Average burden
per response
Total
hours
Youth aged 12 to 17 in the
United States.
Adults 18 and older in the
United States.
Multicultural Youth aged
12–17 in select media
markets.
mstockstill on DSK4VPTVN1PROD with NOTICES
Multicultural youth aged 13–
17 in the select media
markets recruiting through
social media.
Total .............................
1 There
1
13,816
0.0833 (5 min.) .....
1,151
13,816
1
13,816
0.0166 (1 min.) .....
230
41,448
1
41,448
0.0833 (5 min.) .....
3,453
41,448
1
41,448
0.01666 (1 min.) ...
691
2,100
1
2,100
0.5 (30 min.) .........
1,050
Post-test evaluation survey
Pre-test online screener .....
6,300
2,500
1
1
6,300
2,500
0.75 (45 min.) .......
0.0833 (5 min.) .....
4,725
208
Pre-test online survey .........
Post-test online screener ....
Post-test online survey .......
Adults 18 and older in the
United States.
13,816
500
10,500
2,100
1
1
1
500
10,500
2,100
0.5 (30 min.) .........
0.0833 (5 min.) .....
0.75 (45 min.) .......
250
875
1,575
.............................................
134,528
........................
........................
...............................
14,208
are no capital costs or operating and maintenance costs associated with this collection of information.
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E:\FR\FM\13APN1.SGM
13APN1
Federal Register / Vol. 80, No. 70 / Monday, April 13, 2015 / Notices
Dated: April 8, 2015.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2015–08466 Filed 4–10–15; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: HHS–OS–0990–0391–
30D]
Agency Information Collection
Activities; Submission to OMB for
Review and Approval; Public Comment
Request
Information Collection Request Title:
The Hospital Preparedness Program
Office of the Secretary, HHS.
ACTION: Notice.
AGENCY:
In compliance with section
3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, has submitted an
Information Collection Request (ICR),
described below, to the Office of
Management and Budget (OMB) for
review and approval. The ICR is for
reinstatement of a previously-approved
information collection assigned OMB
control number 0990–0391, which
expired on March 31, 2015. Comments
submitted during the first public review
of this ICR will be provided to OMB.
SUMMARY:
OMB will accept further comments from
the public on this ICR during the review
and approval period.
DATES: Comments on the ICR must be
received on or before May 13, 2015.
ADDRESSES: Submit your comments to
OIRA_submission@omb.eop.gov or via
facsimile to (202) 395–5806.
FOR FURTHER INFORMATION CONTACT:
Information Collection Clearance staff,
Information.Collection
Clearance@hhs.gov or (202) 690–6162.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
document identifier HHS–OS–0990–
0391–30D for reference.
OMB No.: 0990–0391.
Abstract: The Science Healthcare
Preparedness Evaluation and Research
(SHARPER), part of the Department of
Health and Human Services (HHS),
Assistant Secretary for Preparedness
and Response (ASPR), Office of
Emergency Management (OEM),
Division of National Healthcare
Preparedness Programs (NHPP), in
conjunction with the Hospital
Preparedness Program (HPP) is seeking
a reinstatement with change on a
currently approved clearance by the
Office of Management of Budget (OMB)
for a Generic Data Collection Form to
19675
serve as the cornerstone of its effort to
assess awardee program under the HPP
Cooperative Agreement (CA) Program.
Program data are gathered from
awardees as part of their Ad-hoc and
End-of-Year Progress Reports and other
similar information collections (ICs)
which have the same general purpose,
account for awardee spending and
program on all activities conducted in
pursuit of achieving the HPP Grant
goals.
This data collection effort is crucial to
HPP’s decision-making process
regarding the continued existence,
design and funding levels of this
program. Results from these data
analyses enable HPP to monitor
healthcare emergency preparedness and
progress towards national preparedness
goals. HPP supports priorities outlined
by the National Preparedness Goal (the
Goal) established by the Department of
Homeland Security (DHS) in 2005. The
Goal guides entities at all levels of
government in the development and
maintenance of capabilities to prevent,
protect against, respond to and recover
from major events. Additionally, the
Goal will assist entities at all levels of
government in the development and
maintenance of the capabilities to
identify, prioritize and protect critical
infrastructure.
Likely Respondents: Hospital
Preparedness Program Awardees.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
respondents
Data collection activity
Number of
responses
Response time
(hours)
Total annual burden
hours
(for all awardees)
3-Year total
(for all awardees)
Generic and Future Program Data Information Collection(s) ................................
62
1
58
3,596
....................................
Total ....................................................
........................
........................
..........................
3,596
10,788
Darius Taylor,
Information Collection Clearance Officer.
[FR Doc. 2015–08298 Filed 4–10–15; 8:45 am]
BILLING CODE 4150–37–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
mstockstill on DSK4VPTVN1PROD with NOTICES
Substance Abuse and Mental Health
Services Administration
Agency Information Collection
Activities: Proposed Collection;
Comment Request
In compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 concerning
opportunity for public comment on
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18:02 Apr 10, 2015
Jkt 235001
proposed collections of information, the
Substance Abuse and Mental Health
Services Administration (SAMHSA)
will publish periodic summaries of
proposed projects. To request more
information on the proposed projects or
to obtain a copy of the information
collection plans, call the SAMHSA
Reports Clearance Officer on (240) 276–
1243.
Comments are invited on: (a) Whether
the proposed collections of information
are 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
PO 00000
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Sfmt 4703
quality, utility, and clarity of the
information to be collected; and (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.
Proposed Project: Primary and
Behavioral Health Care Integration
Program (OMB No. 0930–0340)—
Revision
The Substance Abuse and Mental
Health Services Administration’s
(SAMHSA) Center for Mental Health
Services, (CMHS) is requesting a
revision from the Office of Management
and Budget (OMB) for data collection
activities associated with their Primary
and Behavioral Health Care Integration
E:\FR\FM\13APN1.SGM
13APN1
]]>Agencies
[Federal Register Volume 80, Number 70 (Monday, April 13, 2015)]
[Notices]
[Pages 19673-19675]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-08466]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2014-N-2294]
Agency Information Collection Activities; Submission for Office
of Management and Budget Review; Comment Request; Evaluation of the
Food and Drug Administration's `Fresh Empire' Multicultural Youth
Tobacco Prevention Campaign
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
proposed collection of information has been submitted to the Office of
Management and Budget (OMB) for review and clearance under the
Paperwork Reduction Act of 1995.
DATES: Fax written comments on the collection of information by May 13,
2015.
ADDRESSES: To ensure that comments on the information collection are
received, OMB recommends that written comments be faxed to the Office
of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer,
FAX: 202-395-7285, or emailed to oira_submission@omb.eop.gov. All
comments should be identified with the OMB control number 0910-NEW and
title ``Evaluation of the Food and Drug Administration's `Fresh Empire'
Multicultural Youth Tobacco Prevention Campaign.'' Also include the FDA
docket number found in brackets in the heading of this document.
FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations,
Food and Drug Administration, 8455 Colesville Rd., COLE-14526, Silver
Spring, MD 20993-0002, PRAStaff@ fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has
submitted the following proposed collection of information to OMB for
review and clearance.
Evaluation of the Food and Drug Administration's `Fresh Empire'
Multicultural Youth Tobacco Prevention Campaign (OMB Control Number
0910-NEW)
The 2009 Family Smoking Prevention and Tobacco Control Act (Tobacco
Control Act) (Pub. L. 111-31) amended the Federal Food, Drug, and
Cosmetic Act (the FD&C Act) to grant FDA authority to regulate the
manufacture, marketing, and distribution of tobacco products to protect
public health and to reduce tobacco use by minors. Section
1003(d)(2)(D) of the FD&C Act (21 U.S.C. 393(d)(2)(D)) supports the
development and implementation of FDA public education campaigns
related to tobacco use. Accordingly, FDA is currently developing and
implementing a youth-targeted public education campaign (`Fresh
Empire') to help prevent tobacco use among multicultural youth and
thereby reduce the public health burden of tobacco. The campaign will
feature events, advertisements on television and radio and in print,
digital communications including social media, and other forms of
media.
In support of the provisions of the Tobacco Control Act that
require FDA to protect the public health and to reduce tobacco use by
minors, FDA requests OMB approval to collect information needed to
evaluate FDA's `Fresh Empire' multicultural youth tobacco prevention
campaign. Comprehensive evaluation of FDA's public education campaigns
is needed to ensure campaign messages are effectively received,
understood, and accepted by those for whom they are intended.
Evaluation is an essential organizational practice in public health and
a systematic way to account for and improve public health actions.
FDA plans to evaluate the effectiveness of its multicultural youth
tobacco prevention campaign through an outcome evaluation study that
will be designed to follow the multiple, discrete waves of media
advertising planned for the campaign.
The outcome evaluation study consists of a pre-test survey of
multicultural youth aged 12 to 17 before campaign launch. The pre-test
survey will be followed by ongoing cross-sectional surveys of the
target audience of youth beginning approximately 3 months following
campaign launch. Information will be collected about youth awareness of
and exposure to campaign events and advertisements and about tobacco-
related knowledge, attitudes, beliefs, intentions, and use. Information
will also be collected on demographic variables including age, sex,
race/ethnicity, grade level, and primary language.
All information will be collected through in-person and Web-based
questionnaires. Youth respondents will be recruited from two sources:
(1) A sample drawn from 30 U.S. media markets gathered using an
address-based postal mail sampling of U.S. households for the outcome
evaluation studies and (2) targeted social media
[[Page 19674]]
(e.g., Facebook). Participation in the study is voluntary.
The information collected is necessary to inform FDA's efforts and
measure the effectiveness and public health impact of the campaign.
Data will be used to estimate awareness of and exposure to the campaign
among youth in target markets where the campaign is active. Data will
also be used to examine statistical associations between exposure to
the campaign and subsequent changes in specific outcomes of interest,
which will include knowledge, attitudes, and beliefs, related to
tobacco use.
FDA's burden estimate is based on prior experience with in-person
and Internet panel studies similar to the Agency's plan presented in
this document. Since the 60-day notice published, FDA has revised the
estimated burden. The original burden estimate accounted for evaluation
of more than one FDA multicultural campaign. The current burden
estimate accounts for the evaluation of one campaign, FDA's `Fresh
Empire' Youth Tobacco Prevention Campaign.
A mail-based screener will be one of the methods used to identify
eligible youth. Parents or guardians will be asked to provide consent
and their contact information on this form. For the pre-launch survey,
the 5-minute screener will be completed by 13,816 households for a
total of 1,151 burden hours for youth and an additional 230 hours for
the parents or guardians. For the pre-test survey, 2,100 youth will
complete a questionnaire with an estimated burden of 30 minutes per
respondent, for an annualized total of 1,050 hours. For the post-test
screening survey, the estimated burden is 3,453 hours for youth and 691
hours for adults. For the post-test surveys, the estimated burden is 45
minutes per respondent, for a total of 4,725 burden hours.
We will also recruit youth through social media (e.g., Facebook,
Twitter) as a secondary strategy to recruit youth 13 to 17. An online
version of the screener described above will be used to identify
eligible youth (included in Attachment 3). Eligible youth will be asked
to provide their parents' or guardians' contact information. The
screener will take 5 minutes and will be completed by 2,500 youth for
the pre-test survey for a total of 208 burden hours. Of these, 500 will
be eligible and complete the pre-test survey for a total of 250 burden
hours. For the post-test survey, 10,500 youth will complete the 5-
minute screener, for 875 burden hours. Of these, 2,100 will be eligible
and complete the post-test survey online (up to 45 minutes), for a
total of 1,575 burden hours.
The target number of completed campaign questionnaires for all
respondents is 134,528, and the annualized response burden is estimated
at 14,208 hours.
In the Federal Register of January 5, 2015 (80 FR 230), FDA
published a 60-day notice requesting public comment on the proposed
collection of information. Two comments were received, however, only
one was PRA related.
Comment: One comment stated that the media tracking survey and the
outcome evaluation study proposed by FDA are critical to FDA's efforts
to develop and implement an effective multicultural youth tobacco
prevention campaign.
Response: FDA agrees that this collection of information is
necessary to the Agency's efforts to promote and improve public health.
FDA estimates the burden of this collection of information as
follows:
Table 1--Estimated Annual Reporting Burden \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
Type of respondent Activity Number of responses per Total annual Average burden per response Total
respondents respondent responses hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Youth aged 12 to 17 in the United Screener and Consent 13,816 1 13,816 0.0833 (5 min.)............... 1,151
States. Process--Pre-test
outcome survey.
Adults 18 and older in the United Screener and Consent 13,816 1 13,816 0.0166 (1 min.)............... 230
States. Process--Pre-test
outcome survey.
Youth aged 12 to 17 in the United Screener and Consent 41,448 1 41,448 0.0833 (5 min.)............... 3,453
States. Process--post-test
outcome survey.
Adults 18 and older in the United Screener and Consent 41,448 1 41,448 0.01666 (1 min.).............. 691
States. Process--post-test
outcome survey.
Multicultural Youth aged 12-17 in Pre-test outcome 2,100 1 2,100 0.5 (30 min.)................. 1,050
select media markets. evaluation survey.
Post-test evaluation 6,300 1 6,300 0.75 (45 min.)................ 4,725
survey.
Multicultural youth aged 13-17 in Pre-test online 2,500 1 2,500 0.0833 (5 min.)............... 208
the select media markets recruiting screener.
through social media.
Pre-test online survey. 500 1 500 0.5 (30 min.)................. 250
Post-test online 10,500 1 10,500 0.0833 (5 min.)............... 875
screener.
Post-test online survey 2,100 1 2,100 0.75 (45 min.)................ 1,575
------------------------------------------------------------------------------------------
Total........................... ....................... 134,528 .............. .............. .............................. 14,208
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of information.
[[Page 19675]]
Dated: April 8, 2015.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2015-08466 Filed 4-10-15; 8:45 am]
BILLING CODE 4164-01-P
