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]

Download as PDF 30856 Federal Register / Vol. 79, No. 103 / Thursday, May 29, 2014 / Notices document. If you submit a written petition, two copies are required. A petition submitted electronically must be submitted to https:// www.regulations.gov, Docket No. FDA– 2013–S–0610. Comments and petitions that have not been made publicly available on https://www.regulations.gov may be viewed in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. Dated: May 21, 2014. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2014–12349 Filed 5–28–14; 8:45 am] BILLING CODE 4160–01–P 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 Sfmt 4703 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
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.