Submission for OMB Review; 30-day Comment Request; Web-Based Media Literacy Parent Training for Substance Use Prevention in Rural Locations, 35040-35041 [2013-13795]
Download as PDF
35040
Federal Register / Vol. 78, No. 112 / Tuesday, June 11, 2013 / Notices
order to perform the functions related to
hematopoietic stem cell transplantation
under contract to the U.S. Department of
Health and Human Services (HHS). The
Act requires the Secretary to contract for
the establishment and maintenance of
information related to patients who
have received stem cell therapeutic
products and to do so using a
standardized, electronic format. Data is
collected from transplant centers by the
Center for International Blood and
Marrow Transplant Research and is
used for ongoing analysis of transplant
outcomes. HRSA uses the information
in order to carry out its statutory
responsibilities. Information is needed
to monitor the clinical status of
transplantation and to provide the
Secretary of HHS with an annual report
of transplant center-specific survival
data. The increase in burden, as
reflected in this revised submission
request, is due to an increase in the
annual number of transplants and
increasing survivorship after
transplantation.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose or provide the information
requested. 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. The total annual burden
hours estimated for this ICR are
summarized in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
respondents
Form name
Responses
per
respondent
Total
responses
Hours per
response
Baseline Pre-TED (Transplant Essential Data) ...................
Product Form (includes Infusion, HLA, and Infectious Disease Marker inserts) ........................................................
100-Day Post-TED ...............................................................
6-Month Post-TED ...............................................................
12-Month Post-TED .............................................................
Annual Post-TED .................................................................
200
38
7,600
200
200
200
200
200
29
38
31
27
104
5,800
7,600
6,200
5,400
20,800
1
0.85
1
1
1
5,800
6,460
6,200
5,400
20,800
Total ..............................................................................
200
........................
53,400
........................
52,260
Dated: June 5, 2013.
Bahar Niakan,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2013–13790 Filed 6–10–13; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
wreier-aviles on DSK5TPTVN1PROD with NOTICES
Submission for OMB Review; 30-day
Comment Request; Web-Based Media
Literacy Parent Training for Substance
Use Prevention in Rural Locations
SUMMARY: Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Institute on Drug Abuse, National
Institutes of Health (NIH) 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 March 27, 2013,
pages 18612–18613 and allowed 60days 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 on Drug Abuse
(NIDA), National Institutes of Health,
may not conduct or sponsor, and the
VerDate Mar<15>2010
15:13 Jun 10, 2013
Jkt 229001
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.
Comments 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, submit
comments in writing, or request more
information on the proposed project
contact: Dr. Augie Diana, Health
Scientist Administrator, Prevention
Research Branch, Division of
Epidemiology, Services, and Prevention
Research, NIDA, NIH, 6001 Executive
Boulevard, Room 5163, Bethesda, MD
20892, or call non-toll-free number (301)
443–1942 or Email your request,
including your address to:
PO 00000
Frm 00067
Fmt 4703
Sfmt 4703
1
Total burden
hours
7,600
dianaa@nida.nih.gov. Formal requests
for additional plans and instruments
must be requested in writing.
Proposed Collection: Web-based
Media Literacy Parent Training for
Substance Use Prevention in Rural
Locations, 0925-New, National Institute
on Drug Abuse (NIDA), National
Institutes of Health (NIH).
Need and Use of Information
Collection: This study will develop a
web-based media literacy substance use
prevention intervention for use with
parents and their elementary school
children (approximately ages 7–12), and
will evaluate the program in a
randomized controlled trial to establish
program efficacy in six rural
communities in North Carolina and
Texas. The primary objectives of the
study are to assess the efficacy of a
media literacy education program that is
specifically designed to overcome
barriers to prevention efforts in rural
communities, and to provide the
scientific basis for establishing the
program, Media Detective Family, as an
evidence-based substance use
prevention curriculum. The findings
will provide valuable information
concerning: (1) The appropriateness of
using technology for substance use
prevention programming (i.e., internet,
Smartphone, or tablet-based
applications) to reach rural families
with elementary school-aged children;
E:\FR\FM\11JNN1.SGM
11JNN1
35041
Federal Register / Vol. 78, No. 112 / Tuesday, June 11, 2013 / Notices
(2) improvements in parents’ and
children’s critical thinking skills
associated with intervention exposure;
(3) improvements in parent-child
communication about substances and
the media associated with intervention
exposure; and (4) reductions in
children’s behavioral intentions to use
substances associated with intervention
exposure.
OMB approval is requested for two
years. There are no costs to respondents
other than their time. There are no
capital, operating, and/or maintenance
costs. The total estimated annualized
burden hours are 1067.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Adults:
Permission & Consent ..............................................................................
Pretest ......................................................................................................
Posttest .....................................................................................................
Follow-up ..................................................................................................
Usage Log ................................................................................................
Children:
Assent .......................................................................................................
Pretest ......................................................................................................
Posttest .....................................................................................................
Follow-up ..................................................................................................
Dated: June 5, 2013.
Glenda J. Conroy,
Executive Officer, (OM Director), National
Institute on Drug Abuse, NIH.
[FR Doc. 2013–13795 Filed 6–10–13; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Aging; Notice of
Closed Meetings
wreier-aviles on DSK5TPTVN1PROD with NOTICES
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.
Name of Committee: National Institute on
Aging Special Emphasis Panel SWAN.
Date: June 27, 2013.
Time: 9:30 a.m. to 12:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute on Aging,
Gateway Building, Suite 2C212, 7201
Wisconsin Avenue, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Rebecca Jo Ferrell, Ph.D.,
Scientific Review Branch, National Institute
on Aging, Gateway Building, 7201 Wisconsin
VerDate Mar<15>2010
15:13 Jun 10, 2013
Jkt 229001
Frequency
of response
Average time
per response
200
1
1
1
1
2
10/60
50/60
45/60
45/60
10/60
33.33
166.67
150.00
150.00
67.00
200
1
1
1
1
10/60
50/60
45/60
45/60
33.33
166.67
150.00
150.00
Avenue, Suite 2C212, Bethesda, MD 20892,
301–402–7703, rebecca.ferrell@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.
Name of Committee: National Institute on
Aging Special Emphasis Panel Member
Conflict.
Date: July 29, 2013.
Time: 10:00 a.m. to 11:30 a.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute on Aging,
Gateway Building, Suite 2C212, 7201
Wisconsin Avenue, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Ramesh Vemuri, Ph.D.,
Scientific Review Branch, National Institute
on Aging, Gateway Building, 7201 Wisconsin
Avenue, Suite 2C212, Bethesda, MD 20892,
301–402–7700, rv23r@nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.866, Aging Research,
National Institutes of Health, HHS)
Dated: June 4, 2013.
Melanie J. Gray,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2013–13620 Filed 6–10–13; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
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.
Name of Committee: National Institute of
Biomedical Imaging and Bioengineering
Special Emphasis Panel; NIBIB K Training
Meeting.
Date: July 15, 2013.
Time: 12:30 p.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, DEM
II, 6707 Democracy Blvd., Bethesda, MD
20892, (Telephone Conference Call).
Contact Person: Ruth Grossman, DDS,
Scientific Review Officer, National Institute
of Biomedical Imaging and Bioengineering,
6707 Democracy Boulevard, Room 960,
Bethesda, MD 20892, 301–496–8775,
grossmanrs@mail.nih.gov.
Dated: June 5, 2013.
Melanie J. Gray,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2013–13743 Filed 6–10–13; 8:45 am]
National Institute of Biomedical
Imaging and Bioengineering; Notice of
Closed Meeting
BILLING CODE 4140–01–P
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.
PO 00000
Frm 00068
Fmt 4703
Sfmt 9990
Annual hour
burden
E:\FR\FM\11JNN1.SGM
11JNN1
Agencies
[Federal Register Volume 78, Number 112 (Tuesday, June 11, 2013)]
[Notices]
[Pages 35040-35041]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-13795]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-day Comment Request; Web-Based
Media Literacy Parent Training for Substance Use Prevention in Rural
Locations
SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National Institute on Drug Abuse, National
Institutes of Health (NIH) 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 March 27, 2013, pages
18612-18613 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 on Drug Abuse (NIDA),
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.
Comments 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, submit comments in writing, or
request more information on the proposed project contact: Dr. Augie
Diana, Health Scientist Administrator, Prevention Research Branch,
Division of Epidemiology, Services, and Prevention Research, NIDA, NIH,
6001 Executive Boulevard, Room 5163, Bethesda, MD 20892, or call non-
toll-free number (301) 443-1942 or Email your request, including your
address to: dianaa@nida.nih.gov. Formal requests for additional plans
and instruments must be requested in writing.
Proposed Collection: Web-based Media Literacy Parent Training for
Substance Use Prevention in Rural Locations, 0925-New, National
Institute on Drug Abuse (NIDA), National Institutes of Health (NIH).
Need and Use of Information Collection: This study will develop a
web-based media literacy substance use prevention intervention for use
with parents and their elementary school children (approximately ages
7-12), and will evaluate the program in a randomized controlled trial
to establish program efficacy in six rural communities in North
Carolina and Texas. The primary objectives of the study are to assess
the efficacy of a media literacy education program that is specifically
designed to overcome barriers to prevention efforts in rural
communities, and to provide the scientific basis for establishing the
program, Media Detective Family, as an evidence-based substance use
prevention curriculum. The findings will provide valuable information
concerning: (1) The appropriateness of using technology for substance
use prevention programming (i.e., internet, Smartphone, or tablet-based
applications) to reach rural families with elementary school-aged
children;
[[Page 35041]]
(2) improvements in parents' and children's critical thinking skills
associated with intervention exposure; (3) improvements in parent-child
communication about substances and the media associated with
intervention exposure; and (4) reductions in children's behavioral
intentions to use substances associated with intervention exposure.
OMB approval is requested for two years. There are no costs to
respondents other than their time. There are no capital, operating,
and/or maintenance costs. The total estimated annualized burden hours
are 1067.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Frequency of Average time Annual hour
Type of respondents respondents response per response burden
----------------------------------------------------------------------------------------------------------------
Adults:
Permission & Consent........................ 200 1 10/60 33.33
Pretest..................................... 1 50/60 166.67
Posttest.................................... 1 45/60 150.00
Follow-up................................... 1 45/60 150.00
Usage Log................................... 2 10/60 67.00
Children:
Assent...................................... 200 1 10/60 33.33
Pretest..................................... 1 50/60 166.67
Posttest.................................... 1 45/60 150.00
Follow-up................................... 1 45/60 150.00
----------------------------------------------------------------------------------------------------------------
Dated: June 5, 2013.
Glenda J. Conroy,
Executive Officer, (OM Director), National Institute on Drug Abuse,
NIH.
[FR Doc. 2013-13795 Filed 6-10-13; 8:45 am]
BILLING CODE 4140-01-P