Proposed Collection; Comment Request; Graduate Student Training Program Application, 34692-34693 [E7-12175]
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34692
Federal Register / Vol. 72, No. 121 / Monday, June 25, 2007 / Notices
of screening to improve outcomes for
women exposed to IPV.
Based on the recommendations of a
recent expert panel, in order to provide
this evidence we are proposing to
conduct a randomized controlled trial.
The trial will recruit 3680 women in a
public obstetrics, gynecology, and
family planning clinic. Women
attending this clinic tend to be African
American and of lower socioeconomic
status. For this study (the Main Study),
women will be randomly allocated to
one of three arms: (1) Screened for IPV,
and if disclosing IPV, provided
information on available IPV services;
(2) not screened and all receiving
information on available IPV services; or
(3) a control group that will not be
screened nor receive information on
available IPV services. All three arms
will be assessed with a self-report
measure for mental health, disability,
and quality of life at baseline utilizing
an audio-computer-assisted structured
interview (A–CASI) and at a 12-month
follow-up utilizing a computerizedassisted telephone interview (CATI). A
pretest with 196 women in this same
clinic will be conducted to test the
enrollment, randomization, interview,
and follow-up procedures; provide
estimates for outcome measures and a
potential mediator of outcomes (contact
of IPV services); and establish the
concordance between measures used at
baseline (in the clinic) and at a oneweek follow-up over the phone. The
study arms of the Pretest, which vary
slightly from those of the Main Study,
are designed to accomplish these
intermediate objectives. The results will
be used to refine the measures,
procedures, and sample size
requirements for the Main Study. The
results from the Main Study, the
Randomized Controlled Trial, will guide
CDC as well as other governmental
agencies, professional and health care
organizations, and women’s advocate
groups in formulating its
recommendations and policies
regarding routine screening.
There are no costs to respondents
other than their time to participate in
the survey. The total estimated
annualized burden hours are 717.7.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Respondents
Potential Eligibility for Pretest ......................................................................................................
Pretest Baseline Participants .......................................................................................................
Pretest Follow-up Participants .....................................................................................................
Potential Eligibility for Main Study ...............................................................................................
Main Study Baseline Participants ................................................................................................
Main Study Follow-up Participants ..............................................................................................
Dated: June 19, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–12241 Filed 6–22–07; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
sroberts on PROD1PC70 with NOTICES
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panels (SEP): Risk Factors
for Birth Defects, Request for
Application (RFA) DD 07–001
In accordance with Section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the following meeting:
Time and Date: 9 a.m.–5 p.m., August
1, 2007 (Closed).
Place: Teleconference.
Status: The meeting will be closed to
the public in accordance with
provisions set forth in Section 552b(c)
(4) and (6), Title 5 U.S.C., and the
Determination of the Director,
Management Analysis and Services
VerDate Aug<31>2005
23:08 Jun 22, 2007
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Office, CDC, pursuant to Public Law 92–
463.
Matters To Be Discussed: The meeting
will include the review, discussion, and
evaluation of applications received in
response to ‘‘Risk Factors for Birth
Defects,’’ RFA DD 07–001.
Contact Person for More Information:
Juliana Cyril, Ph.D., Scientific Review
Administrator, Office of Public Health
Research, CDC, 1600 Clifton Road, NE.,
Mailstop D72, Atlanta, GA 30333,
Telephone 404–639–4639.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both CDC
and the Agency for Toxic Substances
and Disease Registry.
Dated: June 18, 2007.
Elaine L. Baker,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. E7–12222 Filed 6–22–07; 8:45 am]
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Number of
responses per
respondents
210
196
176
4600
3680
2580
Average
burden per
response
(in hours)
1
1
1
1
1
1
1/60
15/60
12/60
1/60
17/60
22/60
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment
Request; Graduate Student Training
Program Application
SUMMARY: In compliance with the
requirement of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995,
for opportunity for public comment on
proposed data collection projects, the
Graduate Partnerships Program/OITE/
OIR/OD, the National Institutes of
Health (NIH) will publish periodic
summaries of proposed projects to be
submitted to the Office of Management
and Budget (OMB) for review and
approval.
Proposed Collection
Title: Graduate Student Training
Program Application. Type of
Information Collection Request:
Revision. Form Number: 0925–0501.
Expiration Date: November 30, 2007.
Need and Use of Information Collection:
The information gathered in the
Graduate Student Training Program
application will enable the evaluation
and identification of graduate students
wishing to perform part or all of their
PhD dissertation research within the
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34693
Federal Register / Vol. 72, No. 121 / Monday, June 25, 2007 / Notices
NIH Intramural Research Program (NIH–
IRP). The application for admission into
the Graduate Partnerships Program
(GPP) models many university graduate
school applications, key areas
including: Contact information,
citizenship status, identification of
partnerships to which the student
wishes to apply, educational history,
standardized examination scores, letters
of recommendation, research interests,
personal statement / proposed research,
and NIH investigator for dissertation
research. In addition, race, ethnicity,
gender, and disability questions are
included though optional for
completion; used only for statistical
purposes in evaluating GPP recruiting
efforts and compliance with federal
regulations. The Graduate Student
Training Program application will be
used by the NIH Admission Committees
to identify candidates for admission in
institutional and individual
partnerships.
Frequency of Response: Once.
Affected Public: Individuals. Type of
Respondents: Students pursuing an
advanced degree, Ph.D., who would like
to perform part or all of their
dissertation research in the NIH
Intramural Research Program
laboratories.
The annual reporting burden is
displayed in the following table:
ESTIMATES OF ANNUAL BURDEN HOURS
Estimated
number of respondents
Estimated
number of responses per
respondent
Average burden hours per
response
Estimated total
annual burden
hours requested
Graduate Student Applicants On-Line .............................................................
Post-baccalaureate Applicants On-Line ..........................................................
Collection & Submission of Hardcopy Documents ..........................................
Recommendations (600 × 3) ...........................................................................
Feedback Questions ........................................................................................
100
500
600
1800
200
1
1
1
1
1
0.50
0.50
0.50
0.25
0.25
50
250
300
450
50
Totals ........................................................................................................
3200
........................
........................
1100
Type of respondents
Estimates of capital costs, operating
costs, and/or maintenance costs are
displayed in the following table:
ESTIMATE OF ANNUAL COST TO THE FEDERAL GOVERNMENT
Annualized capital, start-up cost
Amount
Operational/maintenance & purchase components
Amount
Information Collection ...................................................
Application Design, Development, Testing ..................
$0.00
12,000.00
Trouble-shooting and monitoring fees ..........................
Maintenance .................................................................
$2000.00
1000.00
Total .......................................................................
12,000.00
Total .......................................................................
3,000.00
Estimate of Other Total Annual Cost
Burden: $15,000.00.
sroberts on PROD1PC70 with NOTICES
Request for Comments
Written comments and/or suggestions
from the public and affected agencies
should address one or more of the
following points: (1) Evaluate whether
the proposed collection of information
is necessary for the proper performance
of the function of the agency, including
whether the information will have
practical utility; (2) Evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and (4) 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.
VerDate Aug<31>2005
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For Further Information: To request
more information on the proposed
project or to obtain a copy of the data
collection plans and instruments,
contact: Dr. Patricia Wagner, Director of
Admissions & Registrar, Graduate
Partnerships Program, National
Institutes of Health, 2 Center Drive,
Building 2 / Room 2E12, Bethesda,
Maryland 20892–0234, or call 301–594–
9603 or E-mail your request, including
your address to: wagnerpa@od.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60 days of the date of
this publication.
Dated: June 18, 2007.
Michael M. Gottesman,
Deputy Director for Intramural Research,
National Institutes of Health.
[FR Doc. E7–12175 Filed 6–22–07; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions;
Availability for Licensing
National Institutes of Health,
Public Health Service, HHS.
ACTION: Notice.
AGENCY:
SUMMARY: The inventions listed below
are owned by an agency of the U.S.
Government and are available for
licensing in the U.S. in accordance with
35 U.S.C. 207 to achieve expeditious
commercialization of results of
federally-funded research and
development. Foreign patent
applications are filed on selected
inventions to extend market coverage
for companies and may also be available
for licensing.
ADDRESSES: Licensing information and
copies of the U.S. patent applications
listed below may be obtained by writing
to the indicated licensing contact at the
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]]>Agencies
[Federal Register Volume 72, Number 121 (Monday, June 25, 2007)]
[Notices]
[Pages 34692-34693]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-12175]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment Request; Graduate Student Training
Program Application
SUMMARY: In compliance with the requirement of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995, for opportunity for public comment
on proposed data collection projects, the Graduate Partnerships
Program/OITE/OIR/OD, the National Institutes of Health (NIH) will
publish periodic summaries of proposed projects to be submitted to the
Office of Management and Budget (OMB) for review and approval.
Proposed Collection
Title: Graduate Student Training Program Application. Type of
Information Collection Request: Revision. Form Number: 0925-0501.
Expiration Date: November 30, 2007. Need and Use of Information
Collection: The information gathered in the Graduate Student Training
Program application will enable the evaluation and identification of
graduate students wishing to perform part or all of their PhD
dissertation research within the
[[Page 34693]]
NIH Intramural Research Program (NIH-IRP). The application for
admission into the Graduate Partnerships Program (GPP) models many
university graduate school applications, key areas including: Contact
information, citizenship status, identification of partnerships to
which the student wishes to apply, educational history, standardized
examination scores, letters of recommendation, research interests,
personal statement / proposed research, and NIH investigator for
dissertation research. In addition, race, ethnicity, gender, and
disability questions are included though optional for completion; used
only for statistical purposes in evaluating GPP recruiting efforts and
compliance with federal regulations. The Graduate Student Training
Program application will be used by the NIH Admission Committees to
identify candidates for admission in institutional and individual
partnerships.
Frequency of Response: Once. Affected Public: Individuals. Type of
Respondents: Students pursuing an advanced degree, Ph.D., who would
like to perform part or all of their dissertation research in the NIH
Intramural Research Program laboratories.
The annual reporting burden is displayed in the following table:
Estimates of Annual Burden Hours
----------------------------------------------------------------------------------------------------------------
Estimated Estimated
Estimated number of Average burden total annual
Type of respondents number of responses per hours per burden hours
respondents respondent response requested
----------------------------------------------------------------------------------------------------------------
Graduate Student Applicants On-Line............. 100 1 0.50 50
Post-baccalaureate Applicants On-Line........... 500 1 0.50 250
Collection & Submission of Hardcopy Documents... 600 1 0.50 300
Recommendations (600 x 3)....................... 1800 1 0.25 450
Feedback Questions.............................. 200 1 0.25 50
---------------------------------------------------------------
Totals...................................... 3200 .............. .............. 1100
----------------------------------------------------------------------------------------------------------------
Estimates of capital costs, operating costs, and/or maintenance
costs are displayed in the following table:
Estimate of Annual Cost to the Federal Government
----------------------------------------------------------------------------------------------------------------
Operational/maintenance &
Annualized capital, start-up cost Amount purchase components Amount
----------------------------------------------------------------------------------------------------------------
Information Collection........................ $0.00 Trouble-shooting and monitoring $2000.00
fees.
Application Design, Development, Testing...... 12,000.00 Maintenance..................... 1000.00
---------------- ---------------
Total..................................... 12,000.00 Total........................ 3,000.00
----------------------------------------------------------------------------------------------------------------
Estimate of Other Total Annual Cost Burden: $15,000.00.
Request for Comments
Written comments and/or suggestions from the public and affected
agencies should address one or more of the following points: (1)
Evaluate whether the proposed collection of information is necessary
for the proper performance of the function of the agency, including
whether the information will have practical utility; (2) Evaluate the
accuracy of the agency's estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (3) Enhance the quality, utility, and clarity of
the information to be collected; and (4) 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.
For Further Information: To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact: Dr. Patricia Wagner, Director of Admissions &
Registrar, Graduate Partnerships Program, National Institutes of
Health, 2 Center Drive, Building 2 / Room 2E12, Bethesda, Maryland
20892-0234, or call 301-594-9603 or E-mail your request, including your
address to: wagnerpa@od.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 60 days
of the date of this publication.
Dated: June 18, 2007.
Michael M. Gottesman,
Deputy Director for Intramural Research, National Institutes of Health.
[FR Doc. E7-12175 Filed 6-22-07; 8:45 am]
BILLING CODE 4140-01-P
