Submission for OMB Review; 30-Day Comment Request: Generic Clearance to Support the Safe to Sleep Campaign at the Eunice Kennedy Shriver National Institute for Child Health and Human Development (NICHD), 30856-30857 [2014-12370]
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Federal Register / Vol. 79, No. 103 / Thursday, May 29, 2014 / Notices
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Dated: May 21, 2014.
Leslie Kux,
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[FR Doc. 2014–12349 Filed 5–28–14; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day
Comment Request: Generic Clearance
to Support the Safe to Sleep Campaign
at the Eunice Kennedy Shriver National
Institute for Child Health and Human
Development (NICHD)
Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Institute of Child Health and Human
Development, the National Institutes of
Health, has submitted to the Office of
Management and Budget (OMB) a
request for review and approval of the
information collection listed below.
This proposed information collection
was previously published in the Federal
Register on December 30, 2013, pages
79472–79473 and allowed 60-days for
public comment. No public comments
were received. The purpose of this
notice is to allow an additional 30 days
for public comment. The National
Institute of Child Health and Human
Development, National Institutes of
Health, may not conduct or sponsor,
and the respondent is not required to
respond to, an information collection
that has been extended, revised, or
implemented on or after October 1,
1995, unless it displays a currently valid
OMB control number.
Direct Comments to OMB: Written
comments and/or suggestions regarding
the item(s) contained in this notice,
especially regarding the estimated
public burden and associated response
time, should be directed to the: Office
of Management and Budget, Office of
Regulatory Affairs, OIRA_submission@
omb.eop.gov or by fax to 202–395–6974,
Attention: NIH Desk Officer.
tkelley on DSK3SPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
17:19 May 28, 2014
Jkt 232001
Comment Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 30 days of the date of
this publication.
FOR FURTHER INFORMATION CONTACT: To
obtain a copy of the data collection
plans and instruments, or request more
information on the proposed project,
contact: Dr. Sarah L. Glavin, Deputy
Director, Office of Science Policy,
Analysis and Communication, Eunice
Kennedy Shriver National Institute of
Child Health and Human Development,
National Institutes of Health, 31 Center
Drive, Room 2A18, Bethesda, Maryland
20892, or call a non-toll free number
(301) 496–1877 or Email your request,
including your address to glavins@
mail.nih.gov. Formal requests for
additional plans and instruments must
be requested in writing.
Proposed Collection: Generic
Clearance to Support the Safe to Sleep
Campaign at the Eunice Kennedy
Shriver National Institute for Child
Health and Human Development
(NICHD), 0925–NEW, Eunice Kennedy
Shriver National Institute of Child
Health and Human Development
(NICHD), National Institutes of Health
(NIH).
Need and Use of Information
Collection: This is a request for a new
generic clearance that would be used for
submissions specific to the Eunice
Kennedy Shriver National Institute of
Child Health and Human Development
(NICHD) Safe to Sleep (STS) public
education campaign. Submissions for
the STS campaign will be used to assess
the understanding and reach of STS
campaign materials and messages, and
to monitor and improve campaign
activities such as training workshops
and overall implementation. The
purpose of this information collection is
to monitor and modify campaign
activities, to plan future campaign
activities, to develop messages and
materials, and to develop distribution
and outreach strategies that are effective
at communicating their message to bring
about the intended response, awareness,
and/or behavioral change for the target
audiences. This generic clearance will
enable the NICHD to: (1) More
efficiently assess the implementation of
campaign activities; (2) better
understand the target audiences’
knowledge, attitudes, and beliefs toward
STS messages and materials; (3) better
understand how the campaign activities
have influenced the target audiences’
behaviors and practices; and (4) monitor
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
and improve activities such as trainings,
and material/message development.
Having a way to gather feedback on the
STS campaign activities is critical to
assessing the reach and effect of
campaign efforts. Data collected for the
campaign can inform where future STS
campaign resources can produce the
most meaningful results.
Data collected for the STS campaign
generic clearance will be used by a
number of audiences, including STS
campaign staff, NICHD leadership, STS
campaign collaborators, Federal Sudden
and Unexpected Infant Deaths (SUID)/
Sudden Infant Death Syndrome (SIDS)
Workgroup members, SUID/SIDS
stakeholders, clinical and maternal/
child health professionals, parents and
caretakers, and the general public.
These audiences may use the
information collections to: (1) Develop
new campaign messages, materials, and/
or training curricula; (2) monitor and
improve campaign activities; (3) make
decisions about campaign activities; (4)
inform current campaign activities; and
(5) inform and/or change practices and
behaviors of program participants.
Examples of the types of information
collections that could be included under
this generic clearance include: Focus
groups and in-depth interviews with
parents/caregivers and/or health
professionals to get feedback on
distribution and outreach activities,
and/or campaign messages; and Surveys
with parents/caregivers and/or health
professionals to: (1) Assess the
usefulness of the new STS campaign
materials, including print and on-line
materials and a video, (2) track outreach
experiences of program participants, (3)
assess training participants’ changes in
knowledge related to safe infant sleep
behavior and implementation of
outreach methods taught, and (4) assess
program participants’ resource needs.
The sub-studies for this generic will
be small scale, designed to obtain
results frequently and quickly to guide
campaign development and
implementation, inform campaign
direction, and be used internally for
campaign management purposes.
NICHD’s current scope and capacity for
STS generic sub-studies is non-existent
and this request would fill this gap.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
3,000.
Estimated Annualized Burden Hours
E:\FR\FM\29MYN1.SGM
29MYN1
30857
Federal Register / Vol. 79, No. 103 / Thursday, May 29, 2014 / Notices
TABLE 1—ESTIMATES FOR ANNUAL BURDEN HOURS
Number of
respondents
Type of data collection instrument
Frequency of
response
Average time
per response
Annual hour
burden
Focus Groups ..................................................................................................
Pre/Post Test ...................................................................................................
Survey ..............................................................................................................
Interview ...........................................................................................................
Tracking/Feedback Form .................................................................................
500
2,500
2,500
500
1,500
1
1
1
1
1
1
15/60
15/60
1
30/60
500
625
625
500
750
Total ..........................................................................................................
7,500
........................
........................
3,000
(Catalogue of Federal Domestic Assistance
Program Nos. 93.866, Aging Research,
National Institutes of Health, HHS).
[FR Doc. 2014–12370 Filed 5–28–14; 8:45 am]
[FR Doc. 2014–12491 Filed 5–28–14; 8:45 am]
BILLING CODE 4140–01–P
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institutes of Health
National Institute on Aging; Notice of
Closed Meeting
Center for Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The contract proposals and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the contract
proposals, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
tkelley on DSK3SPTVN1PROD with NOTICES
Dated: May 20, 2014.
Sarah L. Glavin,
Deputy Director, Office of Science Policy,
Analysis, and Communications, Eunice
Kennedy Shriver National Institute of Child
Health and Human Development National
Institutes of Health.
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Dated: May 22, 2014.
Melanie J. Gray,
Program Analyst, Office of Federal Advisory
Committee Policy.
Name of Committee: National Institute on
Aging Special Emphasis Panel; Performance
Measure of Multiple Chronic Conditions.
Date: June 2, 2014.
Time: 12:00 p.m. to 1:00 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Institute on Aging,
Gateway Building, Suite 2C212, 7201
Wisconsin Avenue, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Isis S. Mikhail, MPH,
DRPH, National Institute on Aging, Gateway
Building, 7201 Wisconsin Avenue, Suite
2C212, Bethesda, MD 20892, 301–402–7702,
MIKHAILI@mail.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
VerDate Mar<15>2010
17:19 May 28, 2014
Jkt 232001
Name of Committee: Center for Scientific
Review Special Emphasis Panel, PAR13–374:
Modeling of Social Behavior.
Date: June 17, 2014.
Time: 7:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Tomas Drgon, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3152,
MSC 7770, Bethesda, MD 20892, 301–435–
1017, tdrgon@csr.nih.gov.
Name of Committee: Healthcare Delivery
and Methodologies Integrated Review Group,
Biostatistical Methods and Research Design
Study Section.
Date: June 20, 2014.
Time: 8:00 a.m. to 5:00 p.m.
PO 00000
Frm 00054
Fmt 4703
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Agenda: To review and evaluate grant
applications.
Place: Admiral Fell Inn, 888 South
Broadway, Baltimore, MD 21231.
Contact Person: Tomas Drgon, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3152,
MSC 7770, Bethesda, MD 20892, 301–435–
1017, tdrgon@csr.nih.gov.
Name of Committee: Cardiovascular and
Respiratory Sciences Integrated Review
Group, Clinical and Integrative
Cardiovascular Sciences Study Section.
Date: June 26, 2014.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hyatt Regency Bethesda, One
Bethesda Metro Center, 7400 Wisconsin
Avenue, Bethesda, MD 20814.
Contact Person: Delvin R Knight, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive Room 6194
MSC 4128, Bethesda, MD 20892–7814,
301.435.1850, knightdr@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, PAR Panel:
High Throughput Screening Assays for Probe
Discovery.
Date: June 26, 2014.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hyatt Regency Bethesda, One
Bethesda Metro Center, 7400 Wisconsin
Avenue, Bethesda, MD 20814.
Contact Person: Kee Hyang Pyon, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5148,
MSC 7806, Bethesda, MD 20892, pyonkh2@
csr.nih.gov.
Name of Committee: Oncology 1-Basic
Translational Integrated Review Group,
Molecular Oncogenesis Study Section.
Date: June 26, 2014.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Amalfi Hotel, 20 West Kinzie Street,
Chicago, IL 60654.
Contact Person: Nywana Sizemore, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6204,
MSC 7804, Bethesda, MD 20892, 301–435–
1718, sizemoren@csr.nih.gov.
Name of Committee: Cardiovascular and
Respiratory Sciences Integrated Review
E:\FR\FM\29MYN1.SGM
29MYN1
Agencies
[Federal Register Volume 79, Number 103 (Thursday, May 29, 2014)]
[Notices]
[Pages 30856-30857]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-12370]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day Comment Request: Generic
Clearance to Support the Safe to Sleep Campaign at the Eunice Kennedy
Shriver National Institute for Child Health and Human Development
(NICHD)
SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National Institute of Child Health and Human
Development, the National Institutes of Health, has submitted to the
Office of Management and Budget (OMB) a request for review and approval
of the information collection listed below. This proposed information
collection was previously published in the Federal Register on December
30, 2013, pages 79472-79473 and allowed 60-days for public comment. No
public comments were received. The purpose of this notice is to allow
an additional 30 days for public comment. The National Institute of
Child Health and Human Development, National Institutes of Health, may
not conduct or sponsor, and the respondent is not required to respond
to, an information collection that has been extended, revised, or
implemented on or after October 1, 1995, unless it displays a currently
valid OMB control number.
Direct Comments to OMB: Written comments and/or suggestions
regarding the item(s) contained in this notice, especially regarding
the estimated public burden and associated response time, should be
directed to the: Office of Management and Budget, Office of Regulatory
Affairs, OIRA_submission@omb.eop.gov or by fax to 202-395-6974,
Attention: NIH Desk Officer.
Comment Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 30 days
of the date of this publication.
FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data
collection plans and instruments, or request more information on the
proposed project, contact: Dr. Sarah L. Glavin, Deputy Director, Office
of Science Policy, Analysis and Communication, Eunice Kennedy Shriver
National Institute of Child Health and Human Development, National
Institutes of Health, 31 Center Drive, Room 2A18, Bethesda, Maryland
20892, or call a non-toll free number (301) 496-1877 or Email your
request, including your address to glavins@mail.nih.gov. Formal
requests for additional plans and instruments must be requested in
writing.
Proposed Collection: Generic Clearance to Support the Safe to Sleep
Campaign at the Eunice Kennedy Shriver National Institute for Child
Health and Human Development (NICHD), 0925-NEW, Eunice Kennedy Shriver
National Institute of Child Health and Human Development (NICHD),
National Institutes of Health (NIH).
Need and Use of Information Collection: This is a request for a new
generic clearance that would be used for submissions specific to the
Eunice Kennedy Shriver National Institute of Child Health and Human
Development (NICHD) Safe to Sleep (STS) public education campaign.
Submissions for the STS campaign will be used to assess the
understanding and reach of STS campaign materials and messages, and to
monitor and improve campaign activities such as training workshops and
overall implementation. The purpose of this information collection is
to monitor and modify campaign activities, to plan future campaign
activities, to develop messages and materials, and to develop
distribution and outreach strategies that are effective at
communicating their message to bring about the intended response,
awareness, and/or behavioral change for the target audiences. This
generic clearance will enable the NICHD to: (1) More efficiently assess
the implementation of campaign activities; (2) better understand the
target audiences' knowledge, attitudes, and beliefs toward STS messages
and materials; (3) better understand how the campaign activities have
influenced the target audiences' behaviors and practices; and (4)
monitor and improve activities such as trainings, and material/message
development. Having a way to gather feedback on the STS campaign
activities is critical to assessing the reach and effect of campaign
efforts. Data collected for the campaign can inform where future STS
campaign resources can produce the most meaningful results.
Data collected for the STS campaign generic clearance will be used
by a number of audiences, including STS campaign staff, NICHD
leadership, STS campaign collaborators, Federal Sudden and Unexpected
Infant Deaths (SUID)/Sudden Infant Death Syndrome (SIDS) Workgroup
members, SUID/SIDS stakeholders, clinical and maternal/child health
professionals, parents and caretakers, and the general public. These
audiences may use the information collections to: (1) Develop new
campaign messages, materials, and/or training curricula; (2) monitor
and improve campaign activities; (3) make decisions about campaign
activities; (4) inform current campaign activities; and (5) inform and/
or change practices and behaviors of program participants.
Examples of the types of information collections that could be
included under this generic clearance include: Focus groups and in-
depth interviews with parents/caregivers and/or health professionals to
get feedback on distribution and outreach activities, and/or campaign
messages; and Surveys with parents/caregivers and/or health
professionals to: (1) Assess the usefulness of the new STS campaign
materials, including print and on-line materials and a video, (2) track
outreach experiences of program participants, (3) assess training
participants' changes in knowledge related to safe infant sleep
behavior and implementation of outreach methods taught, and (4) assess
program participants' resource needs.
The sub-studies for this generic will be small scale, designed to
obtain results frequently and quickly to guide campaign development and
implementation, inform campaign direction, and be used internally for
campaign management purposes. NICHD's current scope and capacity for
STS generic sub-studies is non-existent and this request would fill
this gap.
OMB approval is requested for 3 years. There are no costs to
respondents other than their time. The total estimated annualized
burden hours are 3,000.
Estimated Annualized Burden Hours
[[Page 30857]]
Table 1--Estimates for Annual Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Frequency of Average time Annual hour
Type of data collection instrument respondents response per response burden
----------------------------------------------------------------------------------------------------------------
Focus Groups.................................... 500 1 1 500
Pre/Post Test................................... 2,500 1 15/60 625
Survey.......................................... 2,500 1 15/60 625
Interview....................................... 500 1 1 500
Tracking/Feedback Form.......................... 1,500 1 30/60 750
---------------------------------------------------------------
Total....................................... 7,500 .............. .............. 3,000
----------------------------------------------------------------------------------------------------------------
Dated: May 20, 2014.
Sarah L. Glavin,
Deputy Director, Office of Science Policy, Analysis, and
Communications, Eunice Kennedy Shriver National Institute of Child
Health and Human Development National Institutes of Health.
[FR Doc. 2014-12370 Filed 5-28-14; 8:45 am]
BILLING CODE 4140-01-P