Proposed Data Collection Submitted for Public Comment and Recommendations, 48534-48536 [2015-19860]
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48534
Federal Register / Vol. 80, No. 156 / Thursday, August 13, 2015 / Notices
tkelley on DSK3SPTVN1PROD with NOTICES
SUPPLEMENTARY INFORMATION:
Background: In 2010, the Deepwater
Horizon oil spill caused extensive
damage to the Gulf Coast’s natural
resources, devastating the economies
and communities that rely on it. In an
effort to help the region rebuild in the
wake of the spill, Congress passed and
the President signed the RESTORE Act,
Public Law 112–141, §§ 1601–1608, 126
Stat. 588 (Jul. 6, 2012). The Act created
the Gulf Coast Ecosystem Restoration
Trust Fund (Trust Fund) and dedicates
eighty percent (80%) of any civil and
administrative penalties paid by parties
responsible for the Deepwater Horizon
oil spill under the Clean Water Act, after
the date of enactment, to the Trust
Fund. The ultimate amount of
administrative and civil penalties
potentially available to the Trust Fund
is currently not certain. On January 3,
2013, the United States announced that
Transocean Deepwater Inc. and related
entities agreed to pay $1 billion in civil
penalties for violating the Clean Water
Act in relation to their conduct in the
Deepwater Horizon oil spill. The
settlement was approved by the court in
February 2013, and pursuant to the Act
approximately $816 million (including
interest) has been paid into the Trust
Fund.
In addition to creating the Trust Fund,
the Act established the Council, which
is chaired by the Secretary of Commerce
and includes the Governors of Alabama,
Florida, Louisiana, Mississippi, and
Texas, and the Secretaries of the U.S.
Departments of Agriculture, the Army,
Homeland Security, and the Interior,
and the Administrator of the U.S.
Environmental Protection Agency.
Under the Act, the Council will
administer a portion of the Trust Fund
known as the Council-Selected
Restoration Component in order to
‘‘undertake projects and programs, using
the best available science, that would
restore and protect the natural
resources, ecosystems, fisheries, marine
and wildlife habitats, beaches, coastal
wetlands, and economy of the Gulf
Coast.’’ In August 2013 the Council
approved an Initial Comprehensive Plan
(Initial Plan) (please see https://
www.restorethegulf.gov/sites/default/
files/GCERCCompPlanFactSheet_0.pdf
and https://www.restorethegulf.gov/sites/
default/files/FinalInitialComprehensive
Plan.pdf) that outlines an overarching
vision for Gulf restoration and includes
the following five goals: (1) Restore and
conserve habitat; (2) restore water
quality; (3) replenish and protect living
coastal and marine resources; (4)
enhance community resilience; and (5)
restore and revitalize the gulf economy.
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16:56 Aug 12, 2015
Jkt 235001
As a supplement to the Initial Plan
and pursuant to the requirement in the
Restore Act to draft a ‘‘prioritized list of
specific projects and programs to be
funded,’’ the Council is now publishing
a draft FPL that proposes the activities
which the Council intends to prioritize
for funding and further consideration.
The Council will carefully review
public and tribal comments, make
appropriate changes, and then finalize
the FPL with appropriate notice in the
Federal Register. Once finalized, the
FPL will serve as the basis for allocating
funds under the Council-Selected
Restoration Component.
The Council seeks public and tribal
comment on all aspects of the draft FPL,
including comments related to the
process used to develop the draft FPL,
the projects and programs contained
therein, and the associated
environmental compliance
documentation.
Summary: The Gulf Coast region is
vital to our nation and our economy,
providing valuable energy resources,
abundant seafood, extraordinary
beaches and recreational activities, and
a rich natural and cultural heritage. Its
waters and coasts are home to one of the
most diverse natural environments in
the world—including over 15,000
species of sea life and millions of
migratory birds. The Gulf has endured
catastrophes, including major
hurricanes such as Katrina, Rita, Gustav
and Ike in the last ten years alone. The
region has also experienced the loss of
critical wetland habitats, erosion of
barrier islands, imperiled fisheries,
water quality degradation and
significant coastal land loss. More
recently, the health of the region’s
ecosystem was significantly affected by
the Deepwater Horizon oil spill. As a
result of the oil spill, the Council has
been given the great responsibility of
helping to address ecological challenges
across the Gulf.
The members of the Council
collaborated in creating a draft FPL that
responds to ecological needs regardless
of jurisdictional boundaries. With the
draft FPL, the Council seeks to provide
near-term ‘‘on-the-ground’’ ecosystem
benefits, while also building a planning
and science foundation for future
success. In the draft FPL, the Council
proposes to focus on ten key watersheds
across the Gulf in order to concentrate
and leverage available funds in
addressing critical ecological needs in
high-priority locations. The draft FPL
focuses on habitat and water quality,
and includes restoration and
conservation activities that can be
implemented in the near term. It also
supports project-specific planning
PO 00000
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efforts necessary to advance large-scale
restoration. The comprehensive
planning and monitoring efforts
proposed in the draft FPL would
provide Gulf-wide benefits into the
future.
The Council intends to play a key role
in helping to ensure that the Gulf’s
natural resources are sustainable and
available for future generations.
Currently available Gulf restoration
funds and those that may become
available in the future represent a great
responsibility. The ongoing involvement
of the people who live, work and play
in the Gulf region is critical to ensuring
that these monies are used wisely and
effectively. The Council thanks all those
who have participated in the process
thus far, and offers thanks in advance to
those who will take the time to again
offer thoughts on how we can
collectively help restore the Gulf.
Document Availability: Copies of the
draft FPL are available at the following
office during regular business hours:
Gulf Coast Ecosystem Restoration
Council, Hale Boggs Federal Building,
500 Poydras Street, Suite 1117, New
Orleans, LA 70130.
Electronic versions of the draft FPL
can be viewed and downloaded at
www.restorethegulf.gov.
Legal Authority: The statutory
program authority for the draft FPL is
found at 33 U.S.C. 1321(t)(2).
Dated: August 13, 2015.
Will D. Spoon,
Program Analyst, Gulf Coast Ecosystem
Restoration Council.
[FR Doc. 2015–19881 Filed 8–12–15; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–15–15BBU]; [Docket No. CDC–
2015–0069]
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 efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
SUMMARY:
E:\FR\FM\13AUN1.SGM
13AUN1
Federal Register / Vol. 80, No. 156 / Thursday, August 13, 2015 / Notices
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection request entitled ‘‘Efficacy
Study of a Mobile Application to
Provide Comprehensive and Medically
Accurate Sexual Health Information for
Adolescent Girls’’. The study will
examine the efficacy of the mobile
application in achieving two behavioral
outcomes: Use of effective contraception
and clinic utilization.
DATES: Written comments must be
received on or before October 13, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0069 by any of the following methods:
Federal eRulemaking Portal:
Regulation.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.
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.
tkelley on DSK3SPTVN1PROD with NOTICES
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 the 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 approval. To
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16:56 Aug 12, 2015
Jkt 235001
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
Efficacy Study of a Mobile
Application to Provide Comprehensive
and Medically Accurate Sexual Health
Information for Adolescent Girls—
New—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Despite drastic reductions in teen
births across all racial and ethnic
groups, Black and Latino girls continue
to have disproportionately high rates of
teen births. Increasing girls’ access to
medically accurate and comprehensive
sexual health information is the first
step in sustaining momentum in teen
pregnancy reduction among all racial
and ethnic groups, and in promoting
healthy sexual behaviors, especially
among minority girls.
CDC plans to collect the information
needed to test the efficacy of a
comprehensive and medically accurate
mobile application, titled Crush, in
increasing adolescent girls’
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48535
contraception use and clinic visitation
for sexual and reproductive health
services. The information disseminated
via Crush is similar to the sexual health
information youth can access via other
Web sites, sexual health promotion
educational materials or in clinics.
The study will randomize a sample of
1,200 girls, ages 14–18, into two groups:
The intervention group and the control
group. The intervention group will have
access to Crush and will receive weekly
sexual health information via text to the
phones for six months. The control
group will have access to a fitness
mobile application (‘‘app’’) and will
receive general health information via
text to their phones for six months.
Participants are expected to access
either app frequently throughout a six
month period. As part of the analysis,
sexual behavior and key psychosocial
factors will be assessed three points in
time: At baseline, and at three- and sixmonth follow-ups.
Efficacy testing will respond to the
following research questions: Research
Question #1 is: Does exposure to Crush
increase consistent contraception use
among participants? We hypothesize
that participants in the intervention
group will report increased intent to use
effective contraception at three and six
months post-intervention. Research
Question #2 is: Does exposure to Crush
increase clinic utilization rate among
participants? We hypothesize that
participants in the intervention group
will report higher rates of intent to
utilize clinic services at three and six
months post intervention.
The study will also include a usability
testing component to identify the
content and features of Crush that are
most attractive to participants, the
frequency in which Crush was used,
and the navigation patterns within
Crush. Participants will create an
account in the Enrollment Database.
This database will host participants’
enrollment information, basic
demographic information, and will also
track their navigation pattern to monitor
Crush visitation frequency and visit
duration. Navigation data will be used
to assess intervention exposure and
dosage to specific content areas of
Crush. To test real-world utilization of
Crush, control group participants will
gain access to Crush six months after
enrolling into the study, but will not
receive weekly text messages. The study
will track visitation frequency and
duration of each visit. Usability testing
will respond to Research Question #3: Is
media content more attractive to
participants? We hypothesize that
participants in the intervention group
E:\FR\FM\13AUN1.SGM
13AUN1
48536
Federal Register / Vol. 80, No. 156 / Thursday, August 13, 2015 / Notices
will spend more time using media
features than text-based content.
All information will be collected
electronically. This study will collect
data through two mechanisms: (1) Selfadministered online surveys, and (2) the
Crush enrollment database. Participants
will complete a total of three selfadministered online surveys at baseline,
three and six month follow-up. Survey
questions will assess behavior, attitudes,
social norms about sexual behavior,
contraception and clinic utilization, and
satisfaction with Crush.
The mobile response surveys will be
sent to participants via text message
which they can complete on a
smartphone. The estimated burden per
response is 13–20 minutes. Survey
and duration of each visit by User ID
and IP address. Web analytics are
generated for any Web site and are a
standard evaluation mechanism for
assessing the traffic patterns on Web
pages. This technology permits
development of an objective and
quantifiable measure that tracks and
records participants’ exposure to Crush.
This study component does not entail
any response burden to participants.
Findings will be used to inform the
development and delivery of effective
health communications.
OMB approval is requested for one
year. Participation is voluntary and
there are no costs to respondents other
than their time.
responses will be matched by each
participant’s unique identifying
number. Each participant will receive
up to two survey reminders starting one
week after the initial survey link is sent,
for two consecutive weeks. There are
minor differences in survey content for
the control and intervention groups.
Each participant will create a profile
in the database upon enrollment. This
database will collect initial
demographic and contact information,
informed consent signatures, and
information about the participant’s
navigation pattern through Crush. Any
information entered directly into Crush
interactive features will not be stored in
the system. The database only collects
web analytics data about page visited
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hrs.)
Total burden
(in hrs.)
Type of respondent
Form name
Girls Ages 14–18 Years ....................
Enrollment ........................................
Consent ............................................
Baseline Survey ...............................
3-Month Follow-up Survey ...............
6-Month Follow-up Survey ...............
Baseline Survey ...............................
3-Month Follow-up Survey ...............
6-Month Follow-up Survey ...............
1,200
1,200
600
600
600
600
600
600
1
1
1
1
1
1
1
1
5/60
5/60
13/60
20/60
20/60
13
20
20
100
100
130
200
200
130
200
200
...........................................................
........................
........................
........................
1,260
Control Group ...................................
Intervention Group ............................
Total ...........................................
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. 2015–19860 Filed 8–12–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Youth Education and
Relationship Services (YEARS)
Descriptive Study.
OMB No.: New Collection,
Description: Since 2006, Congress has
authorized dedicated funding (currently
at the level of $75 million annually) to
support programs providing healthy
marriage and relationship education
(HMRE). In order to better understand
the services that federally-funded HMRE
programs are providing to youth and the
populations the programs are reaching,
The Office of Planning, Research and
Evaluation (OPRE), within ACF/HHS, is
proposing data collection activity as
part of the Youth Education and
Relationship Services (YEARS)
descriptive study. The data that ACF
proposes to collect includes information
on funding spent serving youth, the
number of youth being served, youth
demographic characteristics,
characteristics of the organizations or
programs serving youth, information on
program curricula and contents, and
program implementation information.
This data is to be collected through a
web-based survey that is to be
completed by HMRE grantee program
staff. This information will be critical to
inform future efforts to improve HMRE
programs serving youth.
Respondents: Healthy marriage and
relationship education (HMRE) grantee
program staff.
Note: To fully address the objectives
outlined for this project, it was determined
that additional information collection beyond
what was proposed in the 60 day Federal
Register notice is necessary. Therefore, the
proposed semi-structured interviews
submitted with this request (including the
site visit screener and semi structured
interviews with Program directors/
Administrators, Facilitators, and Partner
organizations/providers) require additional
burden beyond that originally estimated in
the 60 day Federal Register notice.
tkelley on DSK3SPTVN1PROD with NOTICES
ANNUAL BURDEN ESTIMATES
Total/annual
number of
respondents
Instrument
YEARS Web-based staff survey (Program director/Administrator) ...............
YEARS Web-based staff survey (Facilitator) ................................................
Site visit screener (Program director/Administrator) ......................................
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Number of
responses per
respondent
44
44
12
E:\FR\FM\13AUN1.SGM
1
1
1
13AUN1
Average
burden hours
per response
0.5
0.5
0.083
Annual
burden hours
22
22
1
]]>Agencies
[Federal Register Volume 80, Number 156 (Thursday, August 13, 2015)]
[Notices]
[Pages 48534-48536]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-19860]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-15-15BBU]; [Docket No. CDC-2015-0069]
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 efforts to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies to take this opportunity to
[[Page 48535]]
comment on proposed and/or continuing information collections, as
required by the Paperwork Reduction Act of 1995. This notice invites
comment on a proposed information collection request entitled
``Efficacy Study of a Mobile Application to Provide Comprehensive and
Medically Accurate Sexual Health Information for Adolescent Girls''.
The study will examine the efficacy of the mobile application in
achieving two behavioral outcomes: Use of effective contraception and
clinic utilization.
DATES: Written comments must be received on or before October 13, 2015.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2015-
0069 by any of the following methods:
Federal eRulemaking Portal: Regulation.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.
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.
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 the 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 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
Efficacy Study of a Mobile Application to Provide Comprehensive and
Medically Accurate Sexual Health Information for Adolescent Girls--
New--National Center for Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Despite drastic reductions in teen births across all racial and
ethnic groups, Black and Latino girls continue to have
disproportionately high rates of teen births. Increasing girls' access
to medically accurate and comprehensive sexual health information is
the first step in sustaining momentum in teen pregnancy reduction among
all racial and ethnic groups, and in promoting healthy sexual
behaviors, especially among minority girls.
CDC plans to collect the information needed to test the efficacy of
a comprehensive and medically accurate mobile application, titled
Crush, in increasing adolescent girls' contraception use and clinic
visitation for sexual and reproductive health services. The information
disseminated via Crush is similar to the sexual health information
youth can access via other Web sites, sexual health promotion
educational materials or in clinics.
The study will randomize a sample of 1,200 girls, ages 14-18, into
two groups: The intervention group and the control group. The
intervention group will have access to Crush and will receive weekly
sexual health information via text to the phones for six months. The
control group will have access to a fitness mobile application
(``app'') and will receive general health information via text to their
phones for six months. Participants are expected to access either app
frequently throughout a six month period. As part of the analysis,
sexual behavior and key psychosocial factors will be assessed three
points in time: At baseline, and at three- and six-month follow-ups.
Efficacy testing will respond to the following research questions:
Research Question #1 is: Does exposure to Crush increase consistent
contraception use among participants? We hypothesize that participants
in the intervention group will report increased intent to use effective
contraception at three and six months post-intervention. Research
Question #2 is: Does exposure to Crush increase clinic utilization rate
among participants? We hypothesize that participants in the
intervention group will report higher rates of intent to utilize clinic
services at three and six months post intervention.
The study will also include a usability testing component to
identify the content and features of Crush that are most attractive to
participants, the frequency in which Crush was used, and the navigation
patterns within Crush. Participants will create an account in the
Enrollment Database. This database will host participants' enrollment
information, basic demographic information, and will also track their
navigation pattern to monitor Crush visitation frequency and visit
duration. Navigation data will be used to assess intervention exposure
and dosage to specific content areas of Crush. To test real-world
utilization of Crush, control group participants will gain access to
Crush six months after enrolling into the study, but will not receive
weekly text messages. The study will track visitation frequency and
duration of each visit. Usability testing will respond to Research
Question #3: Is media content more attractive to participants? We
hypothesize that participants in the intervention group
[[Page 48536]]
will spend more time using media features than text-based content.
All information will be collected electronically. This study will
collect data through two mechanisms: (1) Self-administered online
surveys, and (2) the Crush enrollment database. Participants will
complete a total of three self-administered online surveys at baseline,
three and six month follow-up. Survey questions will assess behavior,
attitudes, social norms about sexual behavior, contraception and clinic
utilization, and satisfaction with Crush.
The mobile response surveys will be sent to participants via text
message which they can complete on a smartphone. The estimated burden
per response is 13-20 minutes. Survey responses will be matched by each
participant's unique identifying number. Each participant will receive
up to two survey reminders starting one week after the initial survey
link is sent, for two consecutive weeks. There are minor differences in
survey content for the control and intervention groups.
Each participant will create a profile in the database upon
enrollment. This database will collect initial demographic and contact
information, informed consent signatures, and information about the
participant's navigation pattern through Crush. Any information entered
directly into Crush interactive features will not be stored in the
system. The database only collects web analytics data about page
visited and duration of each visit by User ID and IP address. Web
analytics are generated for any Web site and are a standard evaluation
mechanism for assessing the traffic patterns on Web pages. This
technology permits development of an objective and quantifiable measure
that tracks and records participants' exposure to Crush. This study
component does not entail any response burden to participants.
Findings will be used to inform the development and delivery of
effective health communications.
OMB approval is requested for one year. Participation is voluntary
and there are no costs to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondent Form name respondents responses per response (in (in hrs.)
respondent hrs.)
----------------------------------------------------------------------------------------------------------------
Girls Ages 14-18 Years........ Enrollment...... 1,200 1 5/60 100
Consent......... 1,200 1 5/60 100
Control Group................. Baseline Survey. 600 1 13/60 130
3-Month Follow- 600 1 20/60 200
up Survey.
6-Month Follow- 600 1 20/60 200
up Survey.
Intervention Group............ Baseline Survey. 600 1 13 130
3-Month Follow- 600 1 20 200
up Survey.
6-Month Follow- 600 1 20 200
up Survey.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 1,260
----------------------------------------------------------------------------------------------------------------
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. 2015-19860 Filed 8-12-15; 8:45 am]
BILLING CODE 4163-18-P
