Submission for OMB review; Comment Request; 24-hour Dietary Recall Method Comparison and the National Cancer Institute (NCI) Validation and Observational Feeding Studies, 39962-39963 [E9-19022]
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39962
Federal Register / Vol. 74, No. 152 / Monday, August 10, 2009 / Notices
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[FR Doc. E9–19102 Filed 8–7–09; 8:45 am]
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National Institutes of Health
Submission for OMB review; Comment
Request; 24-hour Dietary Recall
Method Comparison and the National
Cancer Institute (NCI) Validation and
Observational Feeding Studies
SUMMARY: Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Cancer Institute (NCI), the National
Institutes of Health (NIH), has submitted
to the Office of Management and Budget
(OMB) a request to review and approve
the information collection listed below.
This proposed information collection
was previously published in the Federal
Register on June 3, 2009 (74 FR 26702)
Number of
respondents
rmajette on DSK29S0YB1PROD with NOTICES
Study Questionnaire
24HR recall comparison study:
Information and Consent ..........................................................................
Screener ...................................................................................................
Dietary Recall 1 ........................................................................................
Dietary Recall 2 ........................................................................................
Demographics questionnaire ....................................................................
VerDate Nov<24>2008
15:09 Aug 07, 2009
Jkt 217001
PO 00000
Frm 00048
Fmt 4703
Sfmt 4703
and allowed 60-days for public
comment. One public comment was
received on June 5 requesting a copy of
the data collection plans. The plans
were sent to the responder on June 10.
The purpose of this notice is to allow an
additional 30 days for public comment.
The 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.
Proposed Collection: Title: 24-hour
Dietary Recall Method Comparison and
the National Cancer Institute (NCI)
Validation and Observational Feeding
Studies. Type of Information Collection
Request: NEW. Need and Use of
Information Collection: The objective of
the two studies is to compare the
performance of the newly developed
computerized Automated SelfAdministered 24-Hour Recall (ASA24)
approach to collecting 24-hour recall
(24HR) data with the current standard,
the interviewer-administered
Automated Multiple Pass Method
(AMPM). The ultimate goal is to
determine to what extent the new
automated instrument can be used
instead of the more expensive
interviewer-administered instrument in
the collection of dietary intake data.
Frequency of Response: Twice. Affected
Public: Individuals. Type of
Respondents: For the 24-hour Dietary
Recall Method Comparison study,
approximately 1,200 adult members
from three health maintenance
organization plans (in Minnesota,
California, and Michigan) between ages
20 and 70 years. For the NCI
Observational Feeding Study,
approximately 90 adult residents from
the Washington, DC metropolitan area
between ages 20 and 70 years. The
annual reporting burden is estimated at
1052 hours (see table below). This
amounts to an estimated 2105 burden
hours over the 2-year data collection
period with a total cost to the
respondents $37,210. There are no
Capital costs, Operating costs, and/or
Maintenance Costs to report.
Average
time
response
(Minutes)
Frequency
of
response
650
600
540
486
540
E:\FR\FM\10AUN1.SGM
1
1
1
1
1
10AUN1
15/60
3/60
30/60
30/60
8/60
Annual hour
burden
162.50
30.00
270.00
243.00
72.00
39963
Federal Register / Vol. 74, No. 152 / Monday, August 10, 2009 / Notices
Average
time
response
(Minutes)
Frequency
of
response
Number of
respondents
Study Questionnaire
Annual hour
burden
243
1
3/60
12.15
Subtotal .............................................................................................
........................
........................
........................
789.65
NCI validation and observational feeding study:
Screener ...................................................................................................
Reminder Telephone Call .........................................................................
Eating 3 meals ..........................................................................................
Dietary Recall ...........................................................................................
Demographics questionnaire ....................................................................
100
90
90
80
80
1
1
1
1
1
3/60
3/60
135/60
30/60
8/60
5.00
4.50
202.50
40.00
10.67
Subtotal .............................................................................................
........................
........................
........................
262.67
Total ...................................................................................................
rmajette on DSK29S0YB1PROD with NOTICES
Preference survey ....................................................................................
........................
........................
........................
1,052.32
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies should
address one or more of the following
points: (1) Whether the proposed
collection of information is necessary
for the proposed performance of the
functions of the agency, including
whether the information may have
practical utility; (2) The accuracy of the
estimate of the burden of the proposed
collection of information including the
validity of the methodology and
assumptions used; (3) Ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
Ways to minimize the burden of the
collection of information on those who
are to respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
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
Attention: NIH Desk Officer, Office of
Management and Budget, at
OIRA_submission@omb.eop.gov or by
fax to 202–395–6974. To request more
information on the proposed project or
to obtain a copy of the data collection
plans, contact Frances E. Thompson,
PhD, Project Officer, National Cancer
Institute, NIH, EPN 4095A, 6130
Executive Boulevard MSC 7335,
Bethesda, Maryland 20892–7335, or call
non-toll-free number 301–594–4410, or
FAX your request to 301–435–3710, or
e-mail your request, including your
address, to thompsof@mail.nih.gov.
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.
VerDate Nov<24>2008
15:09 Aug 07, 2009
Jkt 217001
Dated: July 31, 2009.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National
Institutes of Health.
[FR Doc. E9–19022 Filed 8–7–09; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–N–0366]
Food and Drug Administration,
HHS.
ACTION:
Important dates are as follows:
1. The application due date is
September 7, 2009.
2. The anticipated start date is in
September 2009.
3. The opening date is August 10,
2009.
4. The expiration date is September 8,
2009.
DATES:
FOR FURTHER INFORMATION AND
ADDITIONAL REQUIREMENTS CONTACT:
Nancy Stanisic, Office of Critical Path
Programs (HF–18), rm. 14B45, Food
and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857,
301–827–1660.
Gladys M. Bohler, Grants
Management Specialist, Office of
Frm 00049
Fmt 4703
Funding Opportunity Description
Number: RFA FD–09–019
Catalog of Federal Domestic Assistance
Number: 93.103
A. Background
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of grant funds for the
support of Office of Critical Path
Programs (OCPP). The goal of OCPP is
to develop an administrative and
scientific infrastructure to support the
creation and execution of a series of
projects under the FDA’s Critical Path
Initiative.
PO 00000
SUPPLEMENTARY INFORMATION:
I. Funding Opportunity Description
Office of Critical Path Programs—
Critical Path Initiative
AGENCY:
Acquisitions and Grants Services
(HFA–500), Food and Drug
Administration, 5630 Fishers Lane,
rm. 2105, Rockville, MD 20857,
301–827–7168.
For more information on this funding
opportunity announcement (FOA) and
to obtain detailed requirements, please
refer to the full FOA located at https://
www.fda.gov/oc/initiatives/criticalpath/
.
Sfmt 4703
The Critical Path Initiative, launched
by FDA in 2004, has the objective of
helping modernize the development,
evaluation, manufacture, and use of
FDA-regulated products. Through
nationwide collaboration with other
Federal, academic, scientific, and
industry organizations, the initiative
seeks to develop new tools to facilitate
innovation in FDA-regulated product
development. Examples of tools include
novel biomarkers, laboratory assays,
genetic tests, and state-of-the art
information technologies, etc. In this
initiative, FDA plays the role of a
facilitator in the creation of partnerships
and collaborations to support specific
scientific projects.
B. Research Objectives
FDA’s Office of the Commissioner is
announcing its intent to accept and
consider a single source application for
the award of a Cooperative Agreement
to the Critical Path Institute (C-Path).
FDA anticipates providing up to $1.5
million (direct and indirect costs
combined) during fiscal year (FY) 2009
to support research and related efforts of
E:\FR\FM\10AUN1.SGM
10AUN1
]]>Agencies
[Federal Register Volume 74, Number 152 (Monday, August 10, 2009)]
[Notices]
[Pages 39962-39963]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-19022]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB review; Comment Request; 24-hour Dietary
Recall Method Comparison and the National Cancer Institute (NCI)
Validation and Observational Feeding Studies
SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National Cancer Institute (NCI), the
National Institutes of Health (NIH), has submitted to the Office of
Management and Budget (OMB) a request to review and approve the
information collection listed below. This proposed information
collection was previously published in the Federal Register on June 3,
2009 (74 FR 26702) and allowed 60-days for public comment. One public
comment was received on June 5 requesting a copy of the data collection
plans. The plans were sent to the responder on June 10. The purpose of
this notice is to allow an additional 30 days for public comment. The
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.
Proposed Collection: Title: 24-hour Dietary Recall Method
Comparison and the National Cancer Institute (NCI) Validation and
Observational Feeding Studies. Type of Information Collection Request:
NEW. Need and Use of Information Collection: The objective of the two
studies is to compare the performance of the newly developed
computerized Automated Self-Administered 24-Hour Recall (ASA24)
approach to collecting 24-hour recall (24HR) data with the current
standard, the interviewer-administered Automated Multiple Pass Method
(AMPM). The ultimate goal is to determine to what extent the new
automated instrument can be used instead of the more expensive
interviewer-administered instrument in the collection of dietary intake
data. Frequency of Response: Twice. Affected Public: Individuals. Type
of Respondents: For the 24-hour Dietary Recall Method Comparison study,
approximately 1,200 adult members from three health maintenance
organization plans (in Minnesota, California, and Michigan) between
ages 20 and 70 years. For the NCI Observational Feeding Study,
approximately 90 adult residents from the Washington, DC metropolitan
area between ages 20 and 70 years. The annual reporting burden is
estimated at 1052 hours (see table below). This amounts to an estimated
2105 burden hours over the 2-year data collection period with a total
cost to the respondents $37,210. There are no Capital costs, Operating
costs, and/or Maintenance Costs to report.
----------------------------------------------------------------------------------------------------------------
Average time
Study Questionnaire Number of Frequency of response Annual hour
respondents response (Minutes) burden
----------------------------------------------------------------------------------------------------------------
24HR recall comparison study:
Information and Consent..................... 650 1 15/60 162.50
Screener.................................... 600 1 3/60 30.00
Dietary Recall 1............................ 540 1 30/60 270.00
Dietary Recall 2............................ 486 1 30/60 243.00
Demographics questionnaire.................. 540 1 8/60 72.00
[[Page 39963]]
Preference survey........................... 243 1 3/60 12.15
---------------------------------------------------------------
Subtotal................................ .............. .............. .............. 789.65
===============================================================
NCI validation and observational feeding study:
Screener.................................... 100 1 3/60 5.00
Reminder Telephone Call..................... 90 1 3/60 4.50
Eating 3 meals.............................. 90 1 135/60 202.50
Dietary Recall.............................. 80 1 30/60 40.00
Demographics questionnaire.................. 80 1 8/60 10.67
---------------------------------------------------------------
Subtotal................................ .............. .............. .............. 262.67
===============================================================
Total................................... .............. .............. .............. 1,052.32
----------------------------------------------------------------------------------------------------------------
Request for Comments: Written comments and/or suggestions from the
public and affected agencies should address one or more of the
following points: (1) Whether the proposed collection of information is
necessary for the proposed performance of the functions of the agency,
including whether the information may have practical utility; (2) The
accuracy of the estimate of the burden of the proposed collection of
information including the validity of the methodology and assumptions
used; (3) Ways to enhance the quality, utility, and clarity of the
information to be collected; and (4) Ways to minimize the burden of the
collection of information on those who are to respond, including the
use of appropriate automated, electronic, mechanical, or other
technological collection techniques or other forms of information
technology.
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 Attention: NIH Desk Officer, Office of Management and
Budget, at OIRA_submission@omb.eop.gov or by fax to 202-395-6974. To
request more information on the proposed project or to obtain a copy of
the data collection plans, contact Frances E. Thompson, PhD, Project
Officer, National Cancer Institute, NIH, EPN 4095A, 6130 Executive
Boulevard MSC 7335, Bethesda, Maryland 20892-7335, or call non-toll-
free number 301-594-4410, or FAX your request to 301-435-3710, or e-
mail your request, including your address, to thompsof@mail.nih.gov.
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.
Dated: July 31, 2009.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National Institutes of Health.
[FR Doc. E9-19022 Filed 8-7-09; 8:45 am]
BILLING CODE 4140-01-P
